[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"physical-fitness\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:physical-fitness":27},{"pageToken":4,"total":5,"offset":6,"count":7,"results":8},null,30,0,25,[9,43,77,110,146,171,205,257,282,312,341,367,400,424,450,523,545,575,611,635,671,703,726,752,782],{"id":10,"slug":11,"hasResults":12,"nctId":13,"briefTitle":14,"officialTitle":15,"acronym":4,"eligibilityCriteria":16,"healthyVolunteers":17,"sex":18,"minAge":4,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":4,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":31,"lastUpdatePostDateStruct":32,"startDateStruct":35,"completionDateStruct":37,"leadSponsor":39,"locationsCount":42},"100640124","effects-of-blood-flow-restriction-training-on-body-composition-and-maximal-strength-in-military-personnel-100640124",false,"NCT07628478","Effects of Blood Flow Restriction Training on Body Composition and Maximal Strength in Military Personnel","Effects of Blood Flow Restriction Training on Body Composition and Maximal Strength in Military Personnel: A Prospective Randomized Controlled Trial","Inclusion Criteria:\n\n* Male cadets from military academy;\n* No contraindications to blood flow restriction training (no circulatory diseases, skin allergies);\n* Healthy and capable of high-intensity exercise;\n* Signed informed consent\n\nExclusion Criteria:\n\n* Major sports injury within 2 years (fracture, ligament tear, muscle\u002Ftendon rupture, habitual joint dislocation);\n* Cardiovascular or visceral organ diseases;\n* Other conditions unsuitable for training",true,"ALL",{"count":20,"type":21},36,"ESTIMATED","INTERVENTIONAL",[24],"NA","This study aims to compare the effects of low-intensity blood flow restriction training combined with resistance training versus traditional high-intensity resistance training on body composition (skeletal muscle mass, body fat mass) and maximal strength (isometric mid-thigh pull, vertical jump, isometric squat pull) in male military academy cadets. The study lasts for 6 weeks and adopts a randomized parallel-group design.",[27,28,29],"Physical Fitness","Muscle Strength","Body Composition","RECRUITING","2026-06-04",{"date":33,"type":34},"2026-06-05","ACTUAL",{"date":36,"type":21},"2026-06-01",{"date":38,"type":21},"2026-07-28",{"name":40,"class":41},"Yang Liu","OTHER",1,{"id":44,"slug":45,"hasResults":12,"nctId":46,"briefTitle":47,"officialTitle":47,"acronym":4,"eligibilityCriteria":48,"healthyVolunteers":12,"sex":49,"minAge":50,"maxAge":51,"enrollmentInfo":52,"targetDuration":4,"studyType":22,"phases":54,"briefSummary":55,"conditions":56,"keywords":61,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":69,"lastUpdatePostDateStruct":70,"startDateStruct":72,"completionDateStruct":73,"leadSponsor":75,"locationsCount":4},"100637766","effects-of-moderate-intensity-interval-aerobic-exercise-miiae-on-inflammatory-immune-metabolic-physical-fitness-and-quality-of-life-parameters-in-breast-cancer-patients-undergoing-radiotherapy-100637766","NCT07583719","Effects of Moderate-intensity Interval Aerobic Exercise (MIIAE) on Inflammatory, Immune, Metabolic, Physical Fitness, and Quality of Life Parameters in Breast Cancer Patients Undergoing Radiotherapy.","Inclusion Criteria:\n\n* Women aged between 20 and 65 years.\n* Clinical diagnosis of breast cancer (Stage I-III).\n* Patients who have undergone lumpectomy or mastectomy.\n* Scheduled to start radiotherapy treatment.\n* Sedentary lifestyle according to international physical activity guidelines.\n* Ability to understand and follow instructions.\n* Ability to provide written informed consent.\n\nExclusion Criteria:\n\n* Presence of infectious disease.\n* Cardiovascular or respiratory disease.\n* Metastatic disease.\n* Uncontrolled diabetes mellitus.\n* Neuropathy.\n* Physically active individuals meeting WHO physical activity recommendations.\n* Participation in an exercise intervention program within the last 3 months.\n* Any condition that, in the opinion of the research team, may compromise safety or participation.","FEMALE","20 Years","65 Years",{"count":53,"type":21},40,[24],"Breast cancer and its treatment with radiotherapy may be associated with systemic inflammatory, hematological, cardiac, body composition, functional and quality-of-life alterations. Exercise has emerged as a non-pharmacological strategy with potential benefits during oncological treatment; however, further evidence is needed regarding the effects of supervised moderate-intensity interval aerobic exercise during radiotherapy.\n\nThis randomized controlled trial aims to evaluate the effects of a supervised moderate-intensity interval aerobic exercise programme on systemic inflammatory and immune-derived hematological indices, cardiac biomarkers, body composition, muscle strength, lower-limb power, sleep quality and breast cancer-specific quality of life in women with breast cancer undergoing radiotherapy.\n\nParticipants will be allocated to either an experimental group performing supervised moderate-intensity interval aerobic exercise during radiotherapy or to a control group receiving usual care without structured exercise during the study period. Outcomes will be assessed at baseline and after completion of the intervention period.",[57,58,59,27,60],"Radiotherapy","Inflamation","Immune System","Breast Cancer",[62,63,29,64,65,60,66,67],"Interval Training","Inflammation","Quality of Life","Immune function","Sleep","oncology rehabilitation","NOT_YET_RECRUITING","2026-05-06",{"date":71,"type":34},"2026-05-13",{"date":36,"type":21},{"date":74,"type":21},"2026-12-31",{"name":76,"class":41},"Universidad Francisco de Vitoria",{"id":78,"slug":79,"hasResults":12,"nctId":80,"briefTitle":81,"officialTitle":82,"acronym":4,"eligibilityCriteria":83,"healthyVolunteers":17,"sex":18,"minAge":84,"maxAge":85,"enrollmentInfo":86,"targetDuration":4,"studyType":22,"phases":87,"briefSummary":88,"conditions":89,"keywords":93,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":101,"lastUpdatePostDateStruct":102,"startDateStruct":104,"completionDateStruct":106,"leadSponsor":108,"locationsCount":42},"100635450","effects-of-8-week-crossfit-based-concurrent-training-on-fitness-body-composition-and-psychological-outcomes-in-schoolchildren-100635450","NCT07552844","Effects of 8-Week CrossFit-Based Concurrent Training on Fitness, Body Composition, and Psychological Outcomes in Schoolchildren","Effects of an 8-Week CrossFit-Based Concurrent Training Program on Physical Fitness, Body Composition, and Psychological Outcomes in Schoolchildren: A Randomized Controlled Trial Protocol","Inclusion Criteria:\n\n* Age: 7-11 years.\n* Students enrolled at CEIP Pablo García Baena (Córdoba).\n\nFor the experimental group:\n\n* Availability to attend the Triple XXX Box (Polígono Pedroches, C. los Alfareros, Parcel 119, 14014 Córdoba), where both assessments and training sessions will be conducted.\n* Availability to attend training sessions twice per week for the 8-week intervention period.\n* No participation in extracurricular physical activity prior to the start of the CrossFit program.\n\nFor the control group:\n\nNo participation in extracurricular physical activity. Informed consent signed by parents or legal guardians. No medical, psychological, or behavioral contraindications that would prevent participation in physical activity.\n\nExclusion Criteria:\n\n* Children with musculoskeletal injuries, diseases, or medical, psychological, or behavioral conditions that limit physical activity or interfere with the assessment of outcomes.\n* Inability or anticipated difficulty in regularly attending training sessions.\n* Refusal of parents or legal guardians to provide informed consent.","7 Years","11 Years",{"count":5,"type":21},[24],"This study examines the effects of an 8-week CrossFit-based concurrent training program in boys and girls aged 7 to 11 years, comparing an experimental group (n=15) with a control group (n=15). The aim is to assess changes in strength, cardiorespiratory fitness, body composition, and psychological variables such as anxiety, stress, and self-esteem, using field-based physical tests (CMJ, Course Navette, handgrip strength, etc.) and validated questionnaires. The study follows a randomized controlled trial design with pre- and post-intervention assessments. The experimental group will complete two weekly CrossFit sessions adapted for children, while the control group will maintain their usual routine without structured physical training. The hypothesis states that the intervention will significantly improve both physical performance and psychological well-being in the experimental group compared to the control group.",[90,91,92,27,29],"Children","Crossfit","Psychology, Child",[94,95,96,97,98,99,27,100],"children","stress","anxiety","exercise training","crossfit","self-esteem","body composition","2026-04-25",{"date":103,"type":34},"2026-04-30",{"date":105,"type":21},"2026-06",{"date":107,"type":21},"2026-07",{"name":109,"class":41},"Maimónides Biomedical Research Institute of Córdoba",{"id":111,"slug":112,"hasResults":12,"nctId":113,"briefTitle":114,"officialTitle":115,"acronym":4,"eligibilityCriteria":116,"healthyVolunteers":12,"sex":18,"minAge":117,"maxAge":4,"enrollmentInfo":118,"targetDuration":4,"studyType":120,"phases":4,"briefSummary":121,"conditions":122,"keywords":126,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":137,"lastUpdatePostDateStruct":138,"startDateStruct":140,"completionDateStruct":142,"leadSponsor":144,"locationsCount":42},"100620234","immuno-fit-observational-study-100620234","NCT07354971","IMMUNO-FIT Observational Study","The Immuno-FIT Observational Study: A Phase II Window Observational Study Investigating the Effects of Immunotherapy on Cardiopulmonary Fitness, Quality of Life, and Treatment Outcomes in Patients With Advanced Cancer","Inclusion Criteria:\n\n* Age ≥18 years\n* Histologically confirmed solid malignancy\n* Receiving immune checkpoint inhibitors in one of the following settings:\n\n  * Adjuvant: Single-agent anti-PD-1, anti-PD-L1, or anti-CTLA-4\n  * Metastatic\u002FPalliative: Single-agent or dual-agent anti-PD-1, anti-PD-L1, or anti-CTLA-4\n* ECOG Performance Status 0-2\n* Able to perform cardiopulmonary exercise testing\n* Able to provide written informed consent\n* Willing and able to comply with study procedures and follow-up schedule\n\nExclusion Criteria:\n\n* Age \\\u003C18 years\n* Prior systemic anti-cancer immunotherapy for unresectable or metastatic disease, EXCEPT:\n* Prior adjuvant or neoadjuvant immunotherapy if all treatment-related adverse events have returned to baseline or stabilized\n* Prior anti-PD-1, anti-PD-L1, or anti-CTLA-4 therapy with at least 6 months since last dose and date of disease recurrence\n* Absolute contraindications to cardiopulmonary exercise testing:\n* Acute myocardial infarction within 6 weeks\n* Unstable angina\n* Uncontrolled cardiac arrhythmias causing symptoms or hemodynamic compromise\n* Active endocarditis\n* Symptomatic severe aortic stenosis\n* Uncontrolled heart failure\n* Acute pulmonary embolism or pulmonary infarction\n* Acute myocarditis or pericarditis\n* Suspected or known dissecting aneurysm\n* Acute systemic infection\n* Inability to perform cardiopulmonary exercise testing (e.g., severe lower limb dysfunction, severe peripheral vascular disease)\n* Inability to provide informed consent\n* Currently enrolled in another interventional clinical trial that would confound study outcomes\n\nADDITIONAL EXCLUSION CRITERIA FOR RESEARCH BIOPSY SUB-STUDY:\n\n* Severe cardiopulmonary disease precluding safe sedation (for endoscopic biopsies)\n* Suspected bowel obstruction or perforation (for gastrointestinal biopsies)\n* Uncorrectable severe coagulopathy (INR \\>1.5, platelet count \\\u003C50,000\u002FµL)\n* Severe portal hypertension with high-risk varices (for upper endoscopy)\n* Lesion inaccessible for safe biopsy as determined by a performing clinician","18 Years",{"count":119,"type":21},67,"OBSERVATIONAL","This observational study will investigate how immunotherapy affects physical fitness, quality of life, and treatment tolerance in adults with solid cancers. Immunotherapy can cause a range of side effects that impact daily functioning and may lead to treatment delays or early discontinuation. Physical fitness may influence how well patients cope with treatment, yet little is known about how fitness changes during immunotherapy or whether baseline fitness is linked to outcomes.\n\nParticipants will complete fitness testing using cardiopulmonary exercise testing (CPET) and quality-of-life questionnaires before starting immunotherapy and again 12 weeks later. Blood samples will also be taken, and long-term outcomes including survival, disease progression, and quality of life will be followed for up to 24 months. All cancer treatment will remain standard of care.\n\nA small number of participants will be invited to take part in an optional research biopsy at week 12 to explore how physical fitness relates to changes in the tumour's immune environment.\n\nThe study will help researchers understand natural changes in fitness during immunotherapy, identify whether baseline fitness is associated with treatment tolerance or outcomes, and generate information needed to design future trials testing exercise-based interventions during immunotherapy.",[123,124,27,64,125],"Neoplasms","Immunotherapy","Drug-Related Side Effects and Adverse Reactions",[124,127,27,128,64,129,130,131,132,133,134,135,136],"Immune Checkpoint Inhibitors","Cardiopulmonary Exercise Testing","Immune-Related Adverse Events","Cancer","Exercise Physiology","Tumour Microenvironment","PD-1","PD-L1","CTLA-4","Observational Study","2026-04-22",{"date":139,"type":34},"2026-04-28",{"date":141,"type":34},"2026-03-26",{"date":143,"type":21},"2028-12-31",{"name":145,"class":41},"University Hospital Southampton NHS Foundation Trust",{"id":147,"slug":148,"hasResults":12,"nctId":149,"briefTitle":150,"officialTitle":151,"acronym":4,"eligibilityCriteria":152,"healthyVolunteers":17,"sex":18,"minAge":117,"maxAge":4,"enrollmentInfo":153,"targetDuration":4,"studyType":22,"phases":155,"briefSummary":156,"conditions":157,"keywords":159,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":162,"lastUpdatePostDateStruct":163,"startDateStruct":165,"completionDateStruct":167,"leadSponsor":169,"locationsCount":42},"100632929","xuong-tan-lac-than-exercise-for-range-of-motion-and-muscle-endurance-100632929","NCT07520071","\"Xuong Tan Lac Than\" Exercise for Range of Motion and Muscle Endurance","Assessment of Changes in Range of Motion and Muscle Endurance After Practicing the \"Xuong Tan Lac Than\" Exercise in Healthy Volunteers","INCLUSION CRITERIA\n\n* Aged 18 years or older\n* Voluntarily agree to participate in the study\n* Vital signs within normal limits,\n\nEXCLUSION CRITERIA\n\n* Participants with concomitant internal or surgical medical conditions\n* Refusal to participate in the study at any time\n* Inability to perform or complete the assessment procedures\n* Engaging in vigorous physical activity within 2 days prior to the study participation",{"count":154,"type":21},34,[24],"The goal of this clinical trial is to learn the effects of the \"Xuong tan lac than\" exercise on range of motion and muscle endurance in healthy volunteers. The main questions it aims to answer are:\n\n* Does practicing the \"Xuong tan lac than\" exercise improve joint range of motion (cervical spine, lumbar spine, shoulder, elbow, wrist, knee, and ankle)?\n* Does the exercise improve muscle endurance around these joints?\n\nParticipants will:\n\n* Perform the \"Xuong tan lac than\" exercise for 12 weeks (5 days per week, once daily).\n* Be trained to perform the exercise correctly before starting the intervention.\n* Undergo assessments of joint range of motion and muscle endurance at baseline and after 2, 4, 8, and 12 weeks.",[158,27],"Healthy",[160,161],"Traditional Vietnamese exercise","Xuong tan lac than","2026-04-06",{"date":164,"type":34},"2026-04-09",{"date":166,"type":34},"2026-01-15",{"date":168,"type":21},"2026-09-01",{"name":170,"class":41},"University of Medicine and Pharmacy at Ho Chi Minh City",{"id":172,"slug":173,"hasResults":12,"nctId":174,"briefTitle":175,"officialTitle":176,"acronym":177,"eligibilityCriteria":178,"healthyVolunteers":12,"sex":18,"minAge":117,"maxAge":4,"enrollmentInfo":179,"targetDuration":4,"studyType":22,"phases":181,"briefSummary":182,"conditions":183,"keywords":188,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":197,"lastUpdatePostDateStruct":198,"startDateStruct":200,"completionDateStruct":202,"leadSponsor":203,"locationsCount":4},"100631070","sustainability-of-the-effects-of-an-adapted-physical-activity-program-on-physical-fitness-and-psycho-behavioral-factors-in-patients-with-chronic-diseases-100631070","NCT07495891","Sustainability of the Effects of an Adapted Physical Activity Program on Physical Fitness and Psycho-behavioral Factors in Patients With Chronic Diseases","Sustainability of the Effects of an Adapted Physical Activity Program on Physical Fitness and Psycho-behavioral Factors in Patients With Chronic Diseases: the Influence of Program Duration and the Use of a Smartwatch","DURATECH-APA","Inclusion Criteria:\n\n* Patients over the age of 18\n* French-speaking patients\n* Patients with a chronic condition diagnosed by a doctor\n* Patients with a doctor's prescription for APA\n* Patients capable of understanding instructions\n* Patients enrolled in the Social Security system\n* Patients referred to Maison Sport Santé La Musse by a doctor for the first time\n\nNon inclusion Criteria :\n\n* Medical contraindications to physical exertion\n* Pregnant women\n* Individuals under legal guardianship, conservatorship, or judicial protection.\n* Severe cognitive or motor impairment\n* Lack of proficiency in French\n* Patients in the acute phase requiring specialized care\n* Patients simultaneously participating in another interventional research study\n* Inability to attend sessions regularly or adhere to the schedule of evaluations.\n* Patients who have already completed a program at the Maison Sport Santé\n\nExclusion Criteria:\n\n* Completion of fewer than 16 APA sessions (less than 70% of sessions)\n* Acute exacerbation of a chronic condition during follow-up\n* For groups without smartwatches, the use of a digital tool such as a physical activity tracker by participants would constitute an exclusion criterion\n* Completion of a patient therapeutic education program",{"count":180,"type":21},280,[24],"This study aims to determine the extent to which different approaches to adapted physical activity coaching influence physical fitness, psycho-behavioral, and anthropometric parameters in patients with stabilized chronic conditions who have been referred to a Sport-Health Center by their physician. The trial includes four parallel groups, distinguishing between two program durations (3 months or 6 months) and the use or non-use of a smartwatch as a tool for monitoring activity. All participants complete 24 sessions of adapted physical activity (APA), in accordance with the standard practices of the La Musse Sport-Health Center, where the study is entirely conducted. However, the distribution of sessions differs by group: two sessions per week over three months or one session per week over six months. Randomization is stratified by age, sex, and baseline fitness level. Assessments are conducted at the following five time points: enrollment (T0), end of the 3-month program (T1), end of the 6-month program (T2), followed by follow-up at 12 months (T3) and 18 months (T4), to observe the durability of the effects after the supervised phase. The primary outcome measure is improvement in physical fitness and anthropometric parameters, objectively measured using tests recognized for their reliability (TDM6, Sit-to-Stand 30s, Timed Up and Go, Sit and Reach, grip strength, BMI, waist circumference). The secondary outcomes focus on changes in motivation toward health-related physical activity (EMAPS), perceived self-efficacy to engage in physical activity (ECS), and self-reported physical activity (IPAQ-SF), which will be collected regularly throughout the program, more frequently than in standard care. A total of 280 patients will be enrolled to ensure sufficient statistical power, taking into account an anticipated loss-to-follow-up rate over 18 months. Data collection and processing will be pseudonymized and conducted on the secure network of La Musse Hospital.",[184,185,186,187,27],"Adapted Physical Activity","Smartwatches","Chronic Disease","Motivation for Physical Activity",[189,190,191,192,193,194,195,196],"Adapted physical activity","Chronic diseases","Smartwatch","Sustainability of effects","Motivation for physical activity","Self-efficacy in physical activity","Physical fitness","Longitudinal follow-up","2026-03-23",{"date":199,"type":34},"2026-03-27",{"date":201,"type":21},"2026-03-30",{"date":143,"type":21},{"name":204,"class":41},"Hopital La Musse",{"id":206,"slug":207,"hasResults":12,"nctId":208,"briefTitle":209,"officialTitle":210,"acronym":211,"eligibilityCriteria":212,"healthyVolunteers":17,"sex":213,"minAge":117,"maxAge":214,"enrollmentInfo":215,"targetDuration":4,"studyType":22,"phases":217,"briefSummary":218,"conditions":219,"keywords":234,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":248,"lastUpdatePostDateStruct":249,"startDateStruct":251,"completionDateStruct":253,"leadSponsor":255,"locationsCount":42},"100629969","impact-of-training-load-on-the-gut-microbiome-and-its-relation-to-exercise-performance-muscle-phenotype-and-markers-of-overreaching-in-healthy-men-100629969","NCT07481578","Impact of Training Load on the Gut miCrobiome And Its Relation to exeRcise Performance, mUscle Phenotype, and markerS of Overreaching in Healthy Men","ICARUS: Impact of Training Load on the Gut Microbiome and Its Relation to Exercise Performance, Muscle Phenotype, and Markers of Overreaching in Healthy Men: Phase A - Human Trial","ICARUS","Inclusion criteria:\n\n* Males between 18 and 45 years old.\n* Recreationally active individuals, with a weekly exercise training volume between one and six hours per week.\n* Good health status confirmed by a sport medical screening, which includes a sport medical questionnaire and resting electrocardiogram.\n* Body Mass Index (BMI) between 18.5 and 27.5 kg\u002Fm².\n* Masters the Dutch language.\n\nExclusion criteria:\n\n* Engagement in strenuous competitive sports one month prior to or during the study intervention.\n* Medication and vaccination: Pro- or antibiotic treatment during the past three months, non-steroidal anti-inflammatory drugs (NSAIDs) or cholestyramine during the past month, drugs interfering with intestinal permeability (e.g., prokinetics, laxatives, lubiprostone, loperamide, anti-spasmodics, linaclotide, proton pump inhibitors) during the past month. Vaccinations within one month prior to or during the study intervention.\n* Blood donations within three months or plasma donation within one month prior to or during the study intervention.\n* Inflammatory bowel disease (Crohn or colitis ulcerosa) or celiac disease.\n* Diagnosed irritable bowel syndrome.\n* Intake of any performance-enhancing medication or nutritional supplements known to modulate the gut microbiome in the two months prior to or during the study.\n* Substance abuse, including alcohol consumption of more than three units\u002Fday (weekly average).\n* Any injury or pathology considered a contraindication for performing physical exercise, as determined by the medical doctor overseeing the preparticipation medical screening.\n* No access to smartphone and\u002For computer with internet access.\n* No willingness to use the Polar Flow app and MijnEetmeter to collect physical activity, heart rate, sleep, and food intake data.\n* Concomitant participation in another interventional trial, without approval from the research team.\n* Any other reasons considered by the research team that the participant will not complete the study.","MALE","45 Years",{"count":216,"type":21},45,[24],"The goal of this study is to learn how different amounts of supervised indoor cycling training change gut health (gut bacteria, the substances gut bacteria make, and the gut barrier integrity), and how these changes relate to changes in fitness, muscle health, and signs of doing too much training (a state called 'overreaching'). The study includes healthy, recreationally active men aged 18 to 45 years.\n\nThe primary questions, for which the study is powered (sufficient participants included), are:\n\n1. Does moderate load training change blood and faecal levels of butyrate (a short-chain fatty acid made by gut bacteria) after eight weeks compared with a control group?\n2. Compared to moderate load training, do higher training loads lead to different responses in blood and faecal levels of butyrate?\n\nResearchers will compare:\n\n* A control group that does not complete structured training;\n* A moderate-load training group that completes eight weeks of supervised cycling (4x\u002Fweek);\n* A high-load training group that completes four weeks of moderate-load training followed by four weeks of higher training load (twice the number of training sessions).\n\nParticipants will:\n\n* Be randomly assigned to one of the three groups;\n* Complete 8 weeks of supervised indoor cycling sessions if assigned to a training group;\n* Complete four study assessment periods (baseline, after week four, after week eight, and after a short taper (rest period);\n* Provide blood, stool, skeletal muscle, urine, saliva, and breath samples during the assessment periods;\n* Complete fitness and performance tests and questionnaires during the assessment periods.",[220,221,222,223,224,225,226,227,228,229,27,230,231,232,233],"Exercise","Overreaching","Butyrate","Gut Microbiome","Exercise Performance","Skeletal Muscle","Glucose Tolerance","Hormones","Vascular Health","Muscle Adaptation","Heart Rate Variability (HRV)","Anthropometric Measurements","Metabolic Health","Food Intake",[235,236,237,238,239,240,241,195,221,242,243,244,230,245,246,247],"Exercise training","Training load","Overload training","Fecal butyrate","Gut health","Exercise performance","Muscle phenotype","Glucometabolic health","Vascular health","Muscle adaptation","Anthropometrics","Metabolic health","Food intake","2026-03-16",{"date":250,"type":34},"2026-03-19",{"date":252,"type":34},"2024-10-07",{"date":254,"type":21},"2027-05-31",{"name":256,"class":41},"Stefan De Smet",{"id":258,"slug":259,"hasResults":12,"nctId":260,"briefTitle":261,"officialTitle":262,"acronym":4,"eligibilityCriteria":263,"healthyVolunteers":17,"sex":18,"minAge":117,"maxAge":264,"enrollmentInfo":265,"targetDuration":4,"studyType":120,"phases":4,"briefSummary":266,"conditions":267,"keywords":271,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":273,"lastUpdatePostDateStruct":274,"startDateStruct":276,"completionDateStruct":278,"leadSponsor":280,"locationsCount":42},"100627798","physical-fitness-assessment-in-professional-and-amateur-e-sports-players-100627798","NCT07453316","Physical Fitness Assessment in Professional and Amateur E-Sports Players","Comparing the Physical Fitness Levels of Professional and Amateur E-Sports Players","Inclusion Criteria:\n\n* Adults aged 18 to 30 years\n* Able to read and understand Turkish\n* Professional e-sports players:\n* ≥25 hours per week of structured gaming\n* Affiliated with a competitive team or organization\n* Participates in official tournaments at least once per month\n* Receives income or sponsorship related to gaming\n\nAmateur e-sports players:\n\n* ≤15 hours per week of recreational gaming\n* Not affiliated with a professional team or league\n* Does not receive income or sponsorship from gaming\n* Voluntary agreement to participate and provide informed consent\n\nExclusion Criteria:\n\n* History of respiratory, cardiovascular, or neurological disorders\n* History of surgery within the last 6 months\n* Current use of medication that may affect physical performance\n* Currently undergoing physical therapy or rehabilitation\n* Any musculoskeletal injury that may impair performance during physical fitness testing.","30 Years",{"count":53,"type":21},"The aim of this observational cross-sectional study is to compare the physical fitness characteristics of professional and amateur e-sports players and to determine whether differences exist between the two groups in terms of physical fitness parameters.",[27,268,269,270],"Musculoskeletal Health","Sedentary Behavior","E-Athletes",[272],"E-Sports, Physical Fitness, Professional Gamers, Amateur Gamers, Sedentary Lifestyle, Musculoskeletal Health, Reaction Time, Balance, Aerobic Capacity","2026-03-02",{"date":275,"type":34},"2026-03-05",{"date":277,"type":21},"2026-03-09",{"date":279,"type":21},"2027-03-09",{"name":281,"class":41},"Istinye University",{"id":283,"slug":284,"hasResults":12,"nctId":285,"briefTitle":286,"officialTitle":287,"acronym":288,"eligibilityCriteria":289,"healthyVolunteers":17,"sex":18,"minAge":117,"maxAge":290,"enrollmentInfo":291,"targetDuration":4,"studyType":22,"phases":292,"briefSummary":293,"conditions":294,"keywords":297,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":303,"lastUpdatePostDateStruct":304,"startDateStruct":306,"completionDateStruct":308,"leadSponsor":310,"locationsCount":42},"100622984","diaphragmatic-kinesio-taping-with-hiit-in-trained-individuals-100622984","NCT07390721","Diaphragmatic Kinesio Taping With HIIT in Trained Individuals","Effects of Diaphragmatic Kinesio Taping-Assisted HIIT Exercises on Aerobic Capacity, Anaerobic Capacity, and Balance in Trained Individuals","DKT-HIIT","Inclusion Criteria:\n\n* Aged 18-35 years\n* Male or female trained individuals\n* At least 6 months of regular training history\n* Training at least 3-5 days per week\n* Estimated VO₂max ≥ 50 ml\u002Fkg\u002Fmin\n* No known contraindication to high-intensity exercise\n* No allergy or skin condition preventing kinesio taping\n* Able to provide written informed consent\n\nExclusion Criteria:\n\n* History of cardiovascular, respiratory, or metabolic disease (e.g., asthma, COPD, diabetes, heart disease)\n* Major musculoskeletal injury or surgery within the past 6 months\n* Any pathology affecting diaphragm or respiratory muscles\n* Active smoking or substance abuse\n* Use of performance-enhancing drugs\n* Skin disease in the abdominal region","35 Years",{"count":5,"type":21},[24],"This study examines whether adding diaphragmatic kinesio taping to high-intensity interval training (HIIT) improves physical performance in trained individuals. Participants will be randomly assigned to one of two groups. One group will perform an 8-week HIIT program on a cycle ergometer. The other group will follow the same HIIT program and will also receive diaphragmatic kinesio taping before each exercise session. The taping is applied to support breathing muscles and may help improve oxygen use during exercise.\n\nBefore and after the training period, participants will undergo tests to measure aerobic capacity (VO₂max), anaerobic power (Wingate test), balance (Y-Balance test), lung function (spirometry), body composition, and heart rate responses. The results of this study will help determine whether diaphragmatic kinesio taping provides additional benefits when combined with HIIT training.",[295,27,296],"Postural Balance","Healthy Volunteers",[298,299,300,301,302],"VO2max","Balance","Kinesio Taping","High-Intensity Interval Training","Anaerobic Performance","2026-02-05",{"date":305,"type":34},"2026-02-09",{"date":307,"type":34},"2025-09-01",{"date":309,"type":21},"2026-12-30",{"name":311,"class":41},"Agri Ibrahim Cecen University",{"id":313,"slug":314,"hasResults":12,"nctId":315,"briefTitle":316,"officialTitle":317,"acronym":318,"eligibilityCriteria":319,"healthyVolunteers":17,"sex":18,"minAge":320,"maxAge":4,"enrollmentInfo":321,"targetDuration":4,"studyType":22,"phases":323,"briefSummary":324,"conditions":325,"keywords":329,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":166,"lastUpdatePostDateStruct":333,"startDateStruct":335,"completionDateStruct":337,"leadSponsor":339,"locationsCount":4},"100621023","open-space-and-closed-years-100621023","NCT07365228","Open Space and Closed Years","OPEN SPACE AND CLOSED YEARS","OS&CY","Inclusion Criteria:\n\n* physical fitness status which allows active participation in the physical exercising program organized as a tretment\n\nExclusion Criteria:\n\n* health conditions not allowing the participation in treatment program","50 Years",{"count":322,"type":21},150,[24],"The primary objective of this project is to examine the effects of a specific multicomponent physical activity program (MPAP), conducted in an outdoor setting, on the health and functional-motor status (HFMS) of women over the age of 60. Additionally, the study will investigate the influence of sociodemographic factors (SDF), physical literacy (PL), and health literacy (HL) on the baseline HFMS and the subsequent changes resulting from the KTP.\n\nStudy Methodology\n\nThe program participants will consist of older women (\\>60 years; n=60) whose current HFMS allows for participation in the exercise protocol. They will be divided into two groups:\n\nExperimental Group: Will participate in the MPAP.\n\nControl Group: Will not participate in the MPAP.\n\nThe exercise intervention (MPAP) will include a combination of aerobic activities, strength exercises, balance, and flexibility. It will be conducted two to three times per week across two three-month cycles, separated by a three-month break.\n\nData Collection and Environment Assessments: Sociodemographic factors, physical literacy, and health literacy will be measured at the start of the study. A series of HFMS indicators will be recorded before and after each exercise cycle.\n\nSetting: The MPAP will be performed outdoors in a public park.\n\nProject Significance Beyond analyzing the direct effects of the exercise program and the correlations between the measured variables, this project will contribute to a deeper understanding of the importance of the natural environment in implementing goal-oriented physical activity for the elderly population.",[27,326,327,29,328],"Health Literacy","Lipid Profile","Physical Literacy",[330,331,332],"physical fitness","health status","postmenopausal women",{"date":334,"type":34},"2026-01-26",{"date":336,"type":21},"2026-01-01",{"date":338,"type":21},"2029-06-01",{"name":340,"class":41},"Goran Kuvacic",{"id":342,"slug":343,"hasResults":12,"nctId":344,"briefTitle":345,"officialTitle":345,"acronym":4,"eligibilityCriteria":346,"healthyVolunteers":12,"sex":213,"minAge":117,"maxAge":347,"enrollmentInfo":348,"targetDuration":4,"studyType":22,"phases":349,"briefSummary":350,"conditions":351,"keywords":4,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":358,"lastUpdatePostDateStruct":359,"startDateStruct":361,"completionDateStruct":363,"leadSponsor":365,"locationsCount":42},"100617154","the-effects-of-neuromuscular-training-on-knee-biomechanics-during-jump-landing-among-college-basketball-players-post-acl-reconstruction-and-rehabilitation-100617154","NCT07314931","The Effects of Neuromuscular Training on Knee Biomechanics During Jump-Landing Among College Basketball Players Post ACL Reconstruction and Rehabilitation","Inclusion Criteria:Male college basketball players\n\nAge 18-25 years\n\nHistory of anterior cruciate ligament (ACL) reconstruction surgery at least 12 months before enrollment\n\nCleared by physician for sports participation\n\nWilling to provide informed consent and comply with study procedures\n\nExclusion Criteria:Previous ACL injury on the contralateral knee\n\nOther major lower-limb injuries (e.g., meniscus, cartilage, fractures) in the past 12 months\n\nCurrent knee pain, swelling, or instability that prevents safe participation\n\nNeurological, cardiovascular, or systemic conditions that may affect training safety\n\nParticipation in another structured neuromuscular training program within the past 6 months","25 Years",{"count":5,"type":21},[24],"Basketball players often injure the anterior cruciate ligament (ACL), a key structure that stabilizes the knee. Even after surgery and standard rehabilitation, many athletes continue to have problems with knee stability, movement control, and performance during jumping and landing. These issues increase the risk of re-injury and can limit their ability to return to competition.\n\nNeuromuscular training (NMT) is a type of exercise program that focuses on improving balance, muscle coordination, and movement patterns. It uses activities such as jump-landing drills, balance tasks, agility exercises, and core training. Previous research shows that NMT can help athletes land more safely, reduce harmful knee movements, and improve sport performance. However, little is known about its long-term benefits in college basketball players who are more than one year post-ACL surgery.\n\nThis study aims to evaluate whether a 12-week NMT program, added to standard basketball training, can improve knee biomechanics, stability, and performance in college basketball players with a history of ACL reconstruction. Thirty participants will be randomly assigned to either an NMT group or a control group. Both groups will complete basketball training, but only the NMT group will receive the additional neuromuscular exercises.\n\nKnee movement will be measured using 3D motion capture and force plates, and performance will be tested through vertical jumps and other sport-specific tasks. The main outcomes will include knee angles during landing, ground reaction forces, dynamic stability, and jump height.\n\nThe expected outcome is that athletes who undergo NMT will demonstrate safer landing strategies, better knee control, and improved performance compared to those who only receive standard basketball training. These findings may help coaches and healthcare providers design safer, more effective rehabilitation programs for athletes after ACL surgery.",[352,353,354,355,27,356,357],"Anterior Cruciate Ligament Reconstruction Rehabilitation","Knee Injuries","Biomechanical Data","Athletic Performance","Neuromuscular Training","Basketball Players","2026-01-06",{"date":360,"type":34},"2026-01-07",{"date":362,"type":21},"2025-12-10",{"date":364,"type":21},"2026-05-15",{"name":366,"class":41},"Universiti Sains Malaysia",{"id":368,"slug":369,"hasResults":12,"nctId":370,"briefTitle":371,"officialTitle":372,"acronym":373,"eligibilityCriteria":374,"healthyVolunteers":17,"sex":18,"minAge":117,"maxAge":51,"enrollmentInfo":375,"targetDuration":4,"studyType":22,"phases":377,"briefSummary":378,"conditions":379,"keywords":380,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":390,"lastUpdatePostDateStruct":391,"startDateStruct":393,"completionDateStruct":395,"leadSponsor":397,"locationsCount":399},"100612679","bpit-5-week-multi-site-study-movement-efficiency-mobility--neuromuscular-adaptation-100612679","NCT07256717","BPIT 5-Week Multi-Site Study: Movement Efficiency, Mobility & Neuromuscular Adaptation","Balanced Progressive Intensity Training (BPIT): A Five-Week Multi-Site Clinical Evaluation of Functional Movement, Mobility, and Neuromuscular Adaptation in Healthy Adults (18-65 Years)","BPIT_5LINE_369","Inclusion Criteria:\n\n* Adults aged 18-65 years Generally healthy with regular physical activity history (at least 1-2 sessions per week for the past 3 months) Able to commit to 3-5 supervised training sessions per week for 5 weeks Willing and able to provide written informed consent Cleared by pre-screening (no acute injury, no contraindications)\n\nExclusion Criteria:\n\n* Acute musculoskeletal injury within the past 3 months Known cardiovascular, metabolic, or orthopaedic conditions that contraindicate exercise Pregnancy or planning pregnancy Use of medications or supplements that significantly affect muscle recovery or performance (e.g., corticosteroids, anabolic agents) Inability to follow the BPIT protocol or attend required sessions",{"count":376,"type":21},369,[24],"This prospective, multi-site, single-arm interventional study evaluates the 5-Line Principle of Balanced Progressive Intensity Training (BPIT) over 5 weeks in healthy adults aged 18-65 years. All participants receive supervised BPIT sessions (3-5 per week) progressing through five intensity lines defined by anatomical landmarks and ground reaction force:\n\nGround-Based (Low) Knee-Level (Low-Moderate) Standing (Moderate) Head-Level (Moderate-High) Plyometric (High-Impact)\n\nThe study aims to quantify improvements in functional movement efficiency, joint mobility, postural control, strength adaptation, and heart-rate variability while monitoring safety and individual overload indicators.",[27],[381,382,383,384,385,386,387,388,389],"Balanced Progressive Intensity Training","BPIT","5-Line Principle","Movement Efficiency","Heart Rate Variability","Postural Control","Strength Training","Exercise Intervention","Neuromuscular Adaptation","2025-12-08",{"date":392,"type":34},"2025-12-16",{"date":394,"type":34},"2025-10-10",{"date":396,"type":21},"2026-02-25",{"name":398,"class":41},"MMSx Authority Institute for Movement Mechanics & Biomechanics Research Inc.",10,{"id":401,"slug":402,"hasResults":12,"nctId":403,"briefTitle":404,"officialTitle":405,"acronym":4,"eligibilityCriteria":406,"healthyVolunteers":17,"sex":18,"minAge":117,"maxAge":264,"enrollmentInfo":407,"targetDuration":4,"studyType":22,"phases":409,"briefSummary":410,"conditions":411,"keywords":4,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":415,"lastUpdatePostDateStruct":416,"startDateStruct":418,"completionDateStruct":420,"leadSponsor":422,"locationsCount":42},"100541531","square-step-exercises-in-healthy-young-adults-100541531","NCT06331078","Square Step Exercises in Healthy Young Adults","Comparison of the Effects of Square Step Exercises and Aerobic Exercise on Cognitive Functions and Physical Fitness in Healthy Young Adults","Inclusion Criteria:\n\n* International Physical Activity Questionnaire score \\\u003C600 Metabolic Equivalents (METs),\n* No neurological or orthopedic problems affecting gait, balance and lower extremities\n* No vision or hearing problems, and no history of musculoskeletal surgery.\n\nExclusion Criteria:\n\n* Participants who have pain due to a musculoskeletal problem\n* Participants who are continuing another routine exercise program",{"count":408,"type":21},50,[24],"This study aims to compare the effectiveness of Square Stepping Exercise and aerobic exercise on cognitive function and physical fitness in young adults. Participants aged 18-30 with low physical activity levels will be randomly assigned to either the Square Stepping Exercise Group or Aerobic Exercise Group. Both interventions will be supervised by a physiotherapist, performed twice a week for 40 minutes over 4 weeks. Cognitive function will be assessed using various tests, including attention, short-term memory, and executive function evaluations. Physical fitness will be evaluated through jump tests and balance assessments. Blinded assessors will conduct evaluations at baseline and post-intervention in both groups to determine the impact of square stepping exercise and aerobic exercise on cognitive and physical health in young adults.",[220,412,413,414,27],"Square Step Exercises","Aerobic Exercise","Cognitive Function","2025-08-14",{"date":417,"type":34},"2025-08-19",{"date":419,"type":21},"2025-12-01",{"date":421,"type":21},"2027-12-01",{"name":423,"class":41},"Fenerbahce University",{"id":425,"slug":426,"hasResults":12,"nctId":427,"briefTitle":428,"officialTitle":429,"acronym":4,"eligibilityCriteria":430,"healthyVolunteers":17,"sex":18,"minAge":431,"maxAge":84,"enrollmentInfo":432,"targetDuration":4,"studyType":22,"phases":434,"briefSummary":435,"conditions":436,"keywords":438,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":441,"lastUpdatePostDateStruct":442,"startDateStruct":444,"completionDateStruct":446,"leadSponsor":448,"locationsCount":4},"100602249","influence-of-strength-training-on-myopia-care-in-kindergarten-children-100602249","NCT07121049","Influence of Strength Training on Myopia Care in Kindergarten Children","Study on the Influence of Muscle Strength and Physical Fitness Training on Myopia Health Care for Children in Kindergarten","Inclusion Criteria:\n\n* Children aged 5-7 who are going to be promoted from kindergarten to first grade\n* Must be able to exercise\n\nExclusion Criteria:\n\n* heart disease\n* respiratory problems\n* severe allergies","5 Years",{"count":433,"type":21},120,[24],"With the advancement of technology and changes in lifestyle, the physical activity levels of modern children have gradually decreased. This affects their physical health, psychological development, and social skills, and may increase the risk of nearsightedness. Therefore, it is essential to implement muscle training and outdoor activities in schools, travel agencies, and kindergartens. This project aims to promote the comprehensive development of children through systematic muscle training and enhanced outdoor activities, integrating college students from early childhood education programs, travel agencies, and kindergartens to establish habits that prevent nearsightedness.\n\nIn the kindergarten setting, 60 children in the senior class will serve as the control group, while another 60 will be in the intervention group. The intervention group will participate in 10 weeks of muscle training and outdoor activities, including core exercises 3 times a week for 60 minutes each session from 4pm to 6pm. Additionally, there will be subsidized a total of 2 outdoor activities on weekends. This approach will not only improve the children's coordination and flexibility but also enhance their physical fitness. Regarding travel agencies, tailored outdoor activities specifically designed for young children can be created, such as ecological explorations and wilderness survival training, allowing children to enjoy the fun of movement and learning in a safe environment. Travel agencies should collaborate with educational institutions to provide professional guidance and safety assurances, giving parents peace of mind. For kindergartens, a comprehensive outdoor activity plan should be established, regularly organizing sports days and group competitions to encourage children to participate in team sports like soccer and relay races. This not only helps improve the children's muscle strength but also fosters their spirit of cooperation and social skills. Through these methods, we aim to effectively increase children's activity levels, promote their overall development, and reduce the risk of nearsightedness.",[437,27,28],"Myopia",[439,440,437],"Kindergartens","Muscle training","2025-08-12",{"date":443,"type":34},"2025-08-13",{"date":445,"type":21},"2025-08-20",{"date":447,"type":21},"2026-08-19",{"name":449,"class":41},"Hungkuang University",{"id":451,"slug":452,"hasResults":12,"nctId":453,"briefTitle":454,"officialTitle":455,"acronym":456,"eligibilityCriteria":457,"healthyVolunteers":17,"sex":18,"minAge":458,"maxAge":4,"enrollmentInfo":459,"targetDuration":4,"studyType":120,"phases":4,"briefSummary":461,"conditions":462,"keywords":485,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":514,"lastUpdatePostDateStruct":515,"startDateStruct":517,"completionDateStruct":519,"leadSponsor":521,"locationsCount":42},"100469557","generation-victoria-cohort-2020s-a-statewide-longitudinal-cohort-study-of-victorian-children-and-their-parents-100469557","NCT05394363","Generation Victoria Cohort 2020s: A Statewide Longitudinal Cohort Study of Victorian Children and Their Parents","Generation Victoria Cohort 2020s. A Statewide Longitudinal Cohort of Victorian Children and Their Parents","GenV","Inclusion Criteria (Children):\n\n* Birth date between 4th October 2021 and 3rd October 2023\n* Live at the time of recruitment\n* Residing in Victoria at the time of recruitment\n* Has a legally acceptable representative capable of understanding the informed consent document and providing consent on the child's behalf, who provides a signed and dated informed consent form (e.g. a parent\u002Fguardian)\n\nInclusion Criteria (Adults):\n\n* Be a parent or guardian of a child who meets the eligibility criteria above\n* Provide a signed and dated informed consent form or have a legally acceptable representative capable of understanding the informed consent document and providing consent on the participant's behalf.\n\nExclusion criteria:\n\n* Children who are deceased at the time of recruitment (i.e. still born or died after birth) and their parents\u002Fguardians\n* Families unable to provide informed consent in any of the languages available","1 Day",{"count":460,"type":21},150000,"Generation Victoria (GenV) is a longitudinal, population-based study of Victorian children and their parents that will bring together data on a wide range of conditions ,exposures and outcomes. GenV blends study-collected, study-enhanced and linked data. It will be multi-purpose, supporting observational, interventional, health services and policy research within the same cohort. It is designed to address physical, mental and social issues experienced during childhood, as well as the antecedents of a wide range of diseases of ageing. It seeks to generate translatable evidence (prediction, prevention, treatments, services) to improve future wellbeing and reduce the future disease burden of children and adults.\n\nThe GenV Cohort 2020s is open to all children born over a two-year period, and their parents, residing in the state of Victoria Australia. The GenV Cohort 2020s is preceded by an Advance Cohort of children born between 5 Dec 2020 and 3 October 2021, and their parents. This comprises all families recruited at GenV's Vanguard hospital (Joan Kirner Women's and Children's) and at birthing hospitals throughout Victoria as GenV scaled up to commence recruiting for the GenV Cohort 2020s. The Advance Cohort have ongoing and full participation in GenV for their lifetime unless they withdraw but may have less complete data and biosamples.",[463,464,465,466,467,468,469,64,470,471,472,473,474,475,476,477,478,479,480,27,481,482,483,63,484],"Mental Health","Child Wellbeing","Infant Health","Child Health","Reproductive Health","Healthy Aging","Health Equity","Social Determinants of Health","Environmental Exposure","Genetics","Cognition","Learning","Child Development","Congenital Abnormalities","Disability","Injuries","Communicable Diseases","Noncommunicable Diseases","Diet","Obesity","Allergy and Immunology","Intergenerational Relations",[486,456,487,488,489,466,490,90,491,492,493,494,495,496,497,498,499,500,501,502,503,504,469,505,506,507,508,509,510,511,470,512,513],"Generation Victoria","Cohort Studies","Data Collection","Data Linkage","Midlife Health","Infants","Family","Parents","Mothers","Fathers","Life course perspective","Population Health","Longitudinal Studies","Genetics, population","Demography","Epidemiology","Health Disparity","Minority Health","Vulnerable Populations","Clinical Trial","Randomized Controlled Trial","Pragmatic Clinical Trial","Health Services Research","Economic Models","Value of Life","Geographic Information Systems","Climate Change","Built Environment","2025-07-30",{"date":516,"type":34},"2025-08-03",{"date":518,"type":34},"2021-10-04",{"date":520,"type":21},"2033-10",{"name":522,"class":41},"Murdoch Childrens Research Institute",{"id":524,"slug":525,"hasResults":12,"nctId":526,"briefTitle":527,"officialTitle":527,"acronym":4,"eligibilityCriteria":528,"healthyVolunteers":17,"sex":18,"minAge":320,"maxAge":529,"enrollmentInfo":530,"targetDuration":4,"studyType":120,"phases":4,"briefSummary":532,"conditions":533,"keywords":4,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":536,"lastUpdatePostDateStruct":537,"startDateStruct":539,"completionDateStruct":541,"leadSponsor":543,"locationsCount":42},"100599190","physical-fitness-and-hot-executive-function-in-alzheimers-risk-100599190","NCT07081269","Physical Fitness and Hot Executive Function in Alzheimer's Risk","Inclusion Criteria:\n\n* Age 50-70.\n* Able to engage in fitness testing.\n* Normal vision or corrected-to-normal vision.\n\nExclusion Criteria:\n\n* Suffering from cardiopulmonary-related diseases.\n* Suffering from cognitive, neurological or psychiatric disorders (e.g., dementia, Parkinson's disease, epilepsy, depression, schizophrenia, etc.).\n* Suffering from infectious diseases (e.g., hepatitis, human immunodeficiency virus or Creutzfeldt-Jakob disease).\n* Having a history of drug or alcohol abuse.\n* Having colour vision deficiency (e.g., colour blindness).\n* Having a family history of aneurysm.\n* Taking medications that affect brain function.","70 Years",{"count":531,"type":21},240,"This 18-month study tracks how physical fitness relates to executive function in older adults, aiming to determine if fitness improvements predict better cognitive performance. Participants complete assessments at baseline and 18 months, including cardiorespiratory fitness (YMCA bike test), muscle strength (chest and leg press tests), and executive function (computer tasks with brain activity recording via EEG). Additional measures include physical activity questionnaires, cognitive screening (MMSE), memory tests (digit span), demographics (age, sex, education), and blood tests for APOE ε4 gene status. No exercise program will be provided, allowing observation of natural fitness-cognition relationships in daily life.",[534,535,27],"Executive Function (Cognition)","Event-Related Potentials","2025-07-15",{"date":538,"type":34},"2025-07-23",{"date":540,"type":34},"2025-01-10",{"date":542,"type":21},"2027-07-31",{"name":544,"class":41},"National Taiwan Normal University",{"id":546,"slug":547,"hasResults":12,"nctId":548,"briefTitle":549,"officialTitle":550,"acronym":551,"eligibilityCriteria":552,"healthyVolunteers":17,"sex":18,"minAge":553,"maxAge":4,"enrollmentInfo":554,"targetDuration":4,"studyType":22,"phases":556,"briefSummary":557,"conditions":558,"keywords":563,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":567,"lastUpdatePostDateStruct":568,"startDateStruct":570,"completionDateStruct":571,"leadSponsor":573,"locationsCount":4},"100595529","probiotics-and-active-aging-enhancing-gut-health-100595529","NCT07033637","Probiotics and Active Aging: Enhancing Gut Health","Promoting Health Through Symbiosis: Exploring the Relationship Between Gut Microbiota, Probiotics, and Physical Activity in Older Adults","PAAEGH","Inclusion Criteria:\n\n* Adults aged 60 years or older.\n* Residents of Castilla-La Mancha or Madrid.\n* Able to provide informed consent.\n* For the intervention group: enrolled in a municipal physical activity program with a minimum frequency of 2 sessions per week.\n* Willing to participate in all assessments and follow study instructions.\n* Consent: Participants must provide written informed consent to participate in the study.\n\nExclusion Criteria:\n\n* Recent serious musculoskeletal injuries (e.g., muscle tears, ligament ruptures, fractures).\n* Current symptoms during exercise such as chest pain, dizziness, or joint pain.\n* Uncontrolled hypertension (≥160\u002F100 mmHg).\n* Recent cardiac failure or infectious disease (e.g., meningitis, hepatitis, flu).\n* Chronic gastrointestinal diseases (e.g., Crohn's disease, ulcerative colitis, IBS).\n* Regular use of medications affecting gut motility or microbiota (e.g., laxatives \\>3 times\u002Fweek).\n* Immunodeficiency (e.g., HIV, active cancer).\n* Use of antibiotics (oral or parenteral) within 4 weeks prior to the study.\n* Regular intake of probiotic supplements or foods (e.g., Actimel) within 2 weeks prior to the study.","60 Years",{"count":555,"type":21},90,[24],"The general objective of this clinical trial is to assess the physical fitness and gut microbiota of older adults, thereby highlighting the importance of focusing on health maintenance. By making use of available resources and fostering collaboration among the elements involved in the study, more specific objectives can be defined:\n\n1. To determine the state of the gut flora in older adults through the analysis of the intestinal microbiota.\n2. To identify changes in the intestinal microbiota resulting from the intake of probiotics in older adults.\n3. To evaluate the effects of the intestinal microbiota in older adults participating in a training programme.\n4. To assess the physical fitness and perceived quality of life in older adults who engage in sport activities supported by technology.\n\nParticipants will:\n\n* Perform physical tests such as the 6-Minute Walk Test (6MWT), the Timed Up and Go (TUG), and the Sit-to-Stand test.\n* Complete wellbeing questionnaires to assess their perceived quality of life and health status.\n* Complete dietary habit questionnaires.\n* Provide stool samples for microbiota analysis.\n* Take part in exercise interventions or placebo exercise sessions, depending on their assigned group.",[559,560,561,27,463,562,158],"Gut -Microbiota","Older People","Physical Activity","Probiotic",[564,565,566],"older people","gut microbiota","physical activity","2025-06-13",{"date":569,"type":34},"2025-06-24",{"date":307,"type":21},{"date":572,"type":21},"2026-06-30",{"name":574,"class":41},"Jose Luis Felipe",{"id":576,"slug":577,"hasResults":12,"nctId":578,"briefTitle":579,"officialTitle":579,"acronym":580,"eligibilityCriteria":581,"healthyVolunteers":17,"sex":18,"minAge":50,"maxAge":264,"enrollmentInfo":582,"targetDuration":4,"studyType":22,"phases":583,"briefSummary":584,"conditions":585,"keywords":590,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":604,"lastUpdatePostDateStruct":605,"startDateStruct":607,"completionDateStruct":608,"leadSponsor":609,"locationsCount":4},"100588270","analysis-of-new-materials-and-artificial-turf-products-influence-and-impact-on-athlete-performance-and-perception-100588270","NCT06939218","Analysis of New Materials and Artificial Turf Products: Influence and Impact on Athlete Performance and Perception","ANMATT","Inclusion Criteria: Gender: Male or female football players. Experience: Players who have played football for at least one full season prior to participating in the study.\n\nPlaying Level: Players who have played at the base or amateur level for at least 6 years.\n\nHealth Status: Players who do not have active or chronic injuries that could affect their ability to perform performance tests.\n\nWillingness to Participate: Players who are willing to undergo performance tests and complete perception questionnaires.\n\nRecent Injury History: Players who have not experienced significant injuries in the three months prior to the start of the study.\n\nMedical Conditions: Players who do not have pre-existing medical conditions that could affect their ability to perform performance tests or endanger their health during the tests.\n\nMedication: Players who are not taking medications that could affect their ability to perform performance tests.\n\nConsent: Players who have signed an informed consent form to participate in the study and are willing to consistently follow the study protocols.\n\nAge: Players between 20 and 30 years old (to obtain a more homogeneous sample). -\n\nExclusion Criteria: Recent Injury: Players who have experienced a significant injury in the last three months that required medical attention or could affect their ability to perform performance tests.\n\nChronic Illness: Players who have a chronic illness that could affect their ability to perform performance tests.\n\nMedication: Players who are taking medications that could affect their ability to perform performance tests or could affect their understanding of the questionnaires and perception tools.\n\nMedical History: Players who have a history of cardiovascular, pulmonary, or neurological disease.\n\nRecent Surgery: Players who have had major surgery in the last six months that could affect their ability to perform performance tests.\n\nProtocol Compliance: Players who are not willing or able to consistently follow the study protocols.\n\nDisability: Players who have a physical or cognitive disability that could affect their ability to perform performance tests.\n\nConsent: Players who have not signed an informed consent form to participate in the study.\n\nAge: Players who do not meet the minimum and maximum age requirements to be included in the study.\n\n\\-",{"count":5,"type":21},[24],"This request pertains to a series of related projects on a common theme. Specifically, this set of projects aims to analyze the impact of new alternatives in materials and structures of artificial turf on athlete performance and perception, within the context of the elimination of microplastics as per Commission Regulation (EU) 2023\u002F2055 of September 25, 2023. Third-generation sports artificial turf is notable for including performance infill (granules) that provide the necessary functionality and safety for sports practice. The vast majority of fields worldwide use materials that do not comply with the new European regulation, which has granted an eight-year moratorium. Therefore, there is little time to find new alternatives. The challenge lies not only in developing new structural solutions but also in understanding their impact on athletes. This issue is of high severity, as these sports facilities are the largest in terms of space and host the highest number of Physical Activity and Sports practitioners in Europe (mainly Football, Rugby, Hockey, and Padel).\n\nFor this reason, over the past year, the IGOID Group has requested various projects to cover all the necessary phases and nuances to address this issue.\n\nThe activities included in these projects are divided into two phases:\n\nPhase 1: Evaluation of Sports Surfaces in the Laboratory (durability and surface-player and surface-ball interaction). Tests will be conducted on artificial turf samples constructed with SBR rubber (the main material to be replaced under the EU regulation), natural-origin infills, polymeric infills larger than 5 mm, and other infills. Initially, a market analysis and classification will be carried out, followed by laboratory tests. Across all projects, a minimum of 30 alternatives are expected to be analyzed.\n\nPhase 2: Field Study. Tests will be conducted on a sample of athletes on constructed surfaces representing the different alternatives evaluated in Phase 1. Performance tests and a battery of assessments will be carried out to understand athlete perception. A sample of 30 athletes will be randomly divided into groups to perform different repetitions of the test batteries, covering a minimum of six different sports facilities.",[586,587,27,588,589,158],"Artificial Turf","Athletic Performance and Injury Risk","Sports Equipment","Microplastics",[586,355,27,588,589,591,592,593,594,595,596,597,598,599,600,601,602,603],"Environmental Impact","Athlete Perception","Field Studies","Laboratory Testing","Synthetic Materials","Natural Materials","Polymer Infills","Durability","Safety","Functional Performance","Regulation Compliance","Third-Generation Turf","Football (Soccer)","2025-04-14",{"date":606,"type":34},"2025-04-22",{"date":307,"type":21},{"date":572,"type":21},{"name":610,"class":41},"University of Castilla-La Mancha",{"id":612,"slug":613,"hasResults":12,"nctId":614,"briefTitle":615,"officialTitle":616,"acronym":4,"eligibilityCriteria":617,"healthyVolunteers":12,"sex":18,"minAge":117,"maxAge":4,"enrollmentInfo":618,"targetDuration":4,"studyType":22,"phases":619,"briefSummary":620,"conditions":621,"keywords":4,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":626,"lastUpdatePostDateStruct":627,"startDateStruct":629,"completionDateStruct":631,"leadSponsor":633,"locationsCount":42},"100580033","concurrent-training-in-patients-undergoing-atrial-fibrillation-ablation-100580033","NCT06832033","Concurrent Training in Patients Undergoing Atrial Fibrillation Ablation.","Effects of a Concurrent Physical Exercise Program in Patients Undergoing Atrial Fibrillation Ablation on Fibrillation Burden, Cardiac Morphology and Function, Physical Fitness, Physical Activity, Body Composition and Quality of Life.","Inclusion Criteria:\n\n* Patients aged ≥18 years\n* Undergoing catheter ablation as medical treatment for AF at least one year prior to enrollment.\n\nExclusion Criteria:\n\n* Patients who do not sign the informed consent for participation in the study.\n* Severe atrial dilatation.\n* Structural heart disease.\n* Pathology that prevents the normal practice of intervention with physical exercise",{"count":433,"type":21},[24],"Atrial fibrillation (AF) is an irregular and often very fast heart rhythm, is considered the most common sustained cardiac arrhythmia in adults worldwide, and its incidence and prevalence are increasing. Currently, the estimated prevalence of AF in adults is 2-4%, and is projected to increase 2.3-fold.\n\nAF is associated with increased morbimortality and other comorbidities (hypertension diabetes etc.) which places a significant burden on the patient himself, social health and also on health and social care expenditure.\n\nThe European Society of Cardiology proposes an integrated ABC model (A: Anticoagulation, B: main symptom management, C: optimization of comorbidities and cardiovascular) and within this model, catheter ablation (B) is considered one of the main treatments to control AF symptoms; physical activity (C) is considered one of the modifiable health risk factors and is considered within a lifestyle intervention together with weight loss.\n\nCatheter ablation of AF is currently the treatment of choice for paroxysmal AF. It uses small burns or frostbite to cause some scarring inside the heart to help interrupt the electrical signals that cause the irregular heartbeat. It is a safe procedure that has been shown to be more effective than treatment with antiarrhythmic drugs in reducing the arrhythmic burden and, therefore, the morbidity and mortality associated with the pathology.\n\nMany studies have demonstrated the beneficial effects of moderate physical activity and physical exercise on cardiovascular health. However, there is still controversy as to whether physical activity is associated with an increased risk of AF in the general population; while some studies report a decreased risk of AF, others suggest an increase or that there is no evidence of an association between AF and physical activity.\n\nFew studies have yet focused on the effects of physical activity in those subjects who have undergone catheter ablation. Studies that have evaluated physical activity with questionnaires associate it, when of moderate or high intensity, with lower recurrence of AF and lower incidence of serious events. It is true that the practice of regular and controlled physical exercise is a recognized part of the comprehensive care of patients with coronary heart disease (patients whose heart has difficulty receiving blood), and exercise is systematically identified as a central element of their rehabilitation. However, to date there is no similar approach for AF ablation patients.\n\nGiven the current situation of the subject of interest, the main objective of this project is to study the influence of a physical exercise program in patients undergoing catheter ablation of AF on different morphological and physiological variables of the heart, levels of physical activity and quality of life of patients. Investigators intend to recruit 120 participants, who will be randomly and equally distributed into a group that will perform a physical exercise intervention and a control group that will not perform any type of intervention. Participation in the study will not disrupt the normal practice of the health care system with these patients.",[622,623,561,27,66,64,624,625],"Atrial Fibrillation (AF)","Physical Exercise","Electrocardiogram","Echocardiogram","2025-02-14",{"date":628,"type":34},"2025-02-18",{"date":630,"type":34},"2024-09-09",{"date":632,"type":21},"2026-09",{"name":634,"class":41},"Marcos Echevarría",{"id":636,"slug":637,"hasResults":12,"nctId":638,"briefTitle":639,"officialTitle":640,"acronym":641,"eligibilityCriteria":642,"healthyVolunteers":12,"sex":18,"minAge":51,"maxAge":643,"enrollmentInfo":644,"targetDuration":4,"studyType":22,"phases":646,"briefSummary":647,"conditions":648,"keywords":653,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":662,"lastUpdatePostDateStruct":663,"startDateStruct":665,"completionDateStruct":667,"leadSponsor":669,"locationsCount":42},"100578698","interactive-exergaming-with-otago-exercise-program-on-mobility-in-community-dwelling-older-adults-100578698","NCT06814678","Interactive Exergaming With Otago Exercise Program on Mobility in Community-Dwelling Older Adults","Effectiveness of Interactive Exergaming Combined With the Otago Exercise Program on Mobility in Older Individuals Living in Communities: A Cluster-Randomized Controlled Study","GAME-OEP","Inclusion Criteria:\n\n* Age ≥ 65 years\n* Abnormal mobility based on ICOPE screening (Five-time chair stand test \\> 12 seconds)\n* Able to stand holding handrail for \\> 30 seconds\n\nExclusion Criteria:\n\n* Severe visual impairment\n* Lower limb fracture\n* Acute serious illness\n* Moderate to severe cognitive impairment (SPMSQ \\> 5 errors)\n* Diagnosed psychiatric disorders","99 Years",{"count":645,"type":21},100,[24],"This clinical trial aims to evaluate the effectiveness of interactive exergaming combined with Otago Exercise Program on mobility among community-dwelling older adults aged 65 and above. The main research questions are:\n\nDoes this combined exercise intervention improve elderly mobility? Does this program enhance muscle strength and psychological well-being?\n\nResearchers will compare two groups: one group will do the combined exercise program for 12 weeks, while the other group will continue their usual activities.\n\nParticipants will:\n\n* Have their health checked three times: at the start, after 12 weeks, and 3 months later\n* If in the exercise group, attend exercise sessions twice a week for 12 weeks\n* Complete tests about their physical abilities and how they feel emotionally\n\nWho can take part:\n\n* Adults age 65 or older\n* People who need more than 12 seconds to stand up and sit down 5 times\n* People who can stand for at least 30 seconds with support\n\nPeople cannot take part if they have serious vision problems, recent leg injuries, major illnesses, significant memory problems, or mental health conditions.",[649,650,27,651,652],"Physical Functional Performance","Psychological Health","Mobility Limitation","Aging",[654,655,656,657,658,659,660,661],"Otago Exercise Program","Interactive exergaming","Mobility decline","Community-dwelling older adults","Physical performance","Intrinsic capacity","Psychological health","Muscle strength","2025-02-02",{"date":664,"type":34},"2025-02-07",{"date":666,"type":21},"2025-02-11",{"date":668,"type":21},"2026-03-31",{"name":670,"class":41},"National Taiwan University",{"id":672,"slug":673,"hasResults":12,"nctId":674,"briefTitle":675,"officialTitle":676,"acronym":677,"eligibilityCriteria":678,"healthyVolunteers":17,"sex":18,"minAge":264,"maxAge":51,"enrollmentInfo":679,"targetDuration":4,"studyType":22,"phases":681,"briefSummary":682,"conditions":683,"keywords":684,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":694,"lastUpdatePostDateStruct":695,"startDateStruct":697,"completionDateStruct":699,"leadSponsor":701,"locationsCount":42},"100572010","effect-of-biostrength-training-on-muscle-strength-and-satisfaction-in-adults-aged-30-65-100572010","NCT06727695","Effect of BioStrength Training on Muscle Strength and Satisfaction in Adults Aged 30-65","A Comparative Study of Training Effectiveness: Technogyms Biostrength Devices Vs. Conventional Strength Training Devices: a Randomized Controlled Trial","BIO-STR","Inclusion Criteria:\n\n* • Age between 30 and 65 years\n\n  * Healthy individuals without significant medical conditions\n  * Less than 6 months of prior strength training experience\n  * Willing and able to participate in a 12-week training program\n  * Capable of performing strength training exercises such as leg press and chest press\n  * Able to provide written informed consent\n\nExclusion Criteria:\n\n* • History of coronary heart disease\n\n  * History of stroke\n  * Need for changes in antihypertensive treatment within 3 months prior to study start\n  * Arthritis\n  * Pregnancy or less than three months postpartum\n  * Pain and movement restrictions\n  * Use of medications that affect muscle strength or performance (e.g., anabolic steroids, beta-2 agonists, glucocorticoids, statins, benzodiazepines, ACE inhibitors, angiotensin-II receptor blockers, diuretics)\n  * Any medical condition preventing participation in planned endurance and strength training",{"count":680,"type":21},42,[24],"This study aims to evaluate the effectiveness of Technogyms BioStrength equipment compared to traditional strength training equipment over a 12-week intervention period. The study will determine whether BioStrength machines produce more effective results in terms of muscle strength and body composition. Participants will be allocated to either the BioStrength group or the traditional training group using a minimisation technique to balance important prognostic factors such as handgrip strength, age and gender between the groups. Key measurements include maximum strength tests (10RM) for leg press and chest press, handgrip strength using a dynamometer, and body composition using bioimpedance analysis. Circumference measurements will also be taken. The study will assess whether BioStrength equipment provides superior results in muscle strength, body composition and training efficiency compared to conventional gym equipment.",[28,29,27],[685,661,686,687,688,689,690,691,692,693],"Strength training","Body composition","Customer satisfaction","BioStrength","Technogym","Resistance training","Fitness equipment","Handgrip strength","Randomized controlled trial","2024-12-05",{"date":696,"type":34},"2024-12-11",{"date":698,"type":34},"2024-10-08",{"date":700,"type":21},"2025-10-01",{"name":702,"class":41},"University of Graz",{"id":704,"slug":705,"hasResults":12,"nctId":706,"briefTitle":707,"officialTitle":708,"acronym":709,"eligibilityCriteria":678,"healthyVolunteers":17,"sex":18,"minAge":264,"maxAge":51,"enrollmentInfo":710,"targetDuration":4,"studyType":22,"phases":711,"briefSummary":712,"conditions":713,"keywords":714,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":694,"lastUpdatePostDateStruct":720,"startDateStruct":721,"completionDateStruct":723,"leadSponsor":725,"locationsCount":42},"100572011","comparison-of-two-biocircuit-programs-impact-on-physical-fitness-and-body-composition-in-adults-aged-30-65-100572011","NCT06727708","Comparison of Two BioCircuit Programs: Impact on Physical Fitness and Body Composition in Adults Aged 30-65","A Comparative Study of Two Biocircuit Training Programs:Tone Your Body Vs. Boost Performance on Physical Performance and Body Composition a Randomized Controlled Trial","Biocircuit",{"count":680,"type":21},[24],"This study aims to compare the effects of two BioCircuit training programmes, 'Tone Your Body' and 'Boost Performance', on physical fitness and body composition in adults aged 30-65 years. Participants will be randomized to one of the two exercise programmes and will undergo a 12-week intervention with baseline and post-intervention measurements of fitness and body composition. The study aims to determine which programme is more effective in improving overall physical fitness, muscle mass and reducing body fat.",[28,29,27],[715,685,716,686,195,717,690,718,693,719],"Circle Training","Muscle mass","BioCircuit","Body fat reduction","Handgripstrength",{"date":696,"type":34},{"date":722,"type":34},"2024-10-31",{"date":724,"type":21},"2025-10-31",{"name":702,"class":41},{"id":727,"slug":728,"hasResults":12,"nctId":729,"briefTitle":730,"officialTitle":731,"acronym":4,"eligibilityCriteria":732,"healthyVolunteers":17,"sex":18,"minAge":117,"maxAge":347,"enrollmentInfo":733,"targetDuration":4,"studyType":22,"phases":734,"briefSummary":735,"conditions":736,"keywords":738,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":743,"lastUpdatePostDateStruct":744,"startDateStruct":746,"completionDateStruct":748,"leadSponsor":750,"locationsCount":4},"100560716","effects-of-an-immersive-virtual-reality-program-100560716","NCT06580769","Effects of an Immersive Virtual Reality Program","Effects on Physical Condition and Body Composition of a Physical Exercise Program Implemented Through Immersive Virtual Reality in University Adults: Protocol for a Randomized Controlled Trial","Inclusion Criteria:\n\n* Be a university student\n* Present medical consent authorizing the performance of physical activity\n* Signing of informed consent\n\nExclusion Criteria:\n\n* Have a physical or mental impairment that prevents you from engaging in physical activity\n* Have a vision impairment that does not allow you to use the immersive virtual reality\n* Belong to a special interest group (professional athletes or pregnant women)",{"count":5,"type":21},[24],"A tool that could be useful to eliminate the barriers of not practicing physical activity can be immersive virtual reality, which is characterized by being a technique where a person, through the use of a screen mounted on the head, receives images, sounds and tactile sensations of a simulated world.\n\nIn the area of physical exercise, evidence places immersive virtual reality as a tool that encourages healthy behaviors and the practice of physical activity, increasing adherence to exercise in the long term. In addition to the fact that performing physical activity by this means generates a high level of enjoyment in the participants, so if the use of this technology generates enjoyment in those who use it and contributes to complying with the recommendations of physical activity, it is logical to think that a physical exercise program executed through immersive virtual reality could contribute to improving parameters related to people's health. Therefore, the objective of this randomized controlled trial is to evaluate the effect of a physical exercise program carried out through immersive virtual reality on health-related variables.",[561,737,27],"Virtual Reality",[739,740,741,742],"fat","Muscle","strength","cardiorespiratory fitness","2024-11-18",{"date":745,"type":34},"2024-11-19",{"date":747,"type":21},"2024-12-01",{"date":749,"type":21},"2025-04-30",{"name":751,"class":41},"Universidad Autónoma de Chile",{"id":753,"slug":754,"hasResults":12,"nctId":755,"briefTitle":756,"officialTitle":756,"acronym":757,"eligibilityCriteria":758,"healthyVolunteers":17,"sex":18,"minAge":85,"maxAge":759,"enrollmentInfo":760,"targetDuration":4,"studyType":22,"phases":762,"briefSummary":763,"conditions":764,"keywords":766,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":773,"lastUpdatePostDateStruct":774,"startDateStruct":776,"completionDateStruct":778,"leadSponsor":780,"locationsCount":42},"100535654","effectiveness-of-a-multicomponent-intervention-to-promote-physical-activity-levels-during-the-school-day-moveschool-100535654","NCT06254638","Effectiveness of a Multicomponent Intervention to Promote Physical Activity Levels During the School Day (MOVESCHOOL)","MOVESCHOOL","Inclusion Criteria:\n\n* Adolescents in 1st, 2nd and 3rd year of ESO.\n* Adolescents with informed consent signed by the family\u002Fguardian.\n* Schools with at least 80 students enrolled in 1st, 2nd and 3rd ESO.\n* Schools belonging to the regions of Cáceres and Cádiz.\n\nExclusion Criteria:\n\n* Adolescents with any physical disability or health condition that may limit physical activity levels.\n* Schools participating in any other physical activity or health promotion program.","16 Years",{"count":761,"type":21},900,[24],"Study based a multicomponent school-based intervention during the school-day (i.e., Physically active learning, active breaks, and active recess) on Physical Activity, health, educational, and cognition outcomes in adolescents.",[561,765,27,473],"Adolescents",[767,768,769,770,771,772],"Active Break","Physically active learning","Active Recess","Motivational variables","Sedentary time","Academic indicators","2024-09-12",{"date":775,"type":34},"2024-09-19",{"date":777,"type":34},"2023-09-01",{"date":779,"type":21},"2026-08-31",{"name":781,"class":41},"University of Extremadura",{"id":783,"slug":784,"hasResults":12,"nctId":785,"briefTitle":786,"officialTitle":786,"acronym":787,"eligibilityCriteria":788,"healthyVolunteers":17,"sex":18,"minAge":85,"maxAge":759,"enrollmentInfo":789,"targetDuration":4,"studyType":22,"phases":791,"briefSummary":792,"conditions":793,"keywords":794,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":796,"lastUpdatePostDateStruct":797,"startDateStruct":798,"completionDateStruct":800,"leadSponsor":802,"locationsCount":42},"100561433","effectiveness-of-integrating-physically-active-learning-through-co-teaching-in-extremadura-activa-mente-project-100561433","NCT06590103","Effectiveness of Integrating Physically Active Learning Through Co-teaching in Extremadura: ACTIVA-MENTE Project","ACTIVA-MENTE","Inclusion Criteria:\n\n* Adolescents in 1st, 2nd, 3rd and 4th year of ESO.\n* Adolescents with informed consent signed by the family\u002Fguardian.\n* Schools with at least 210 students enrolled in 1st, 2nd, 3rd and 4th year of ESO.\n* Schools belonging to the Autonomous Community of Extremadura.\n\nExclusion Criteria:\n\n* Adolescents with any physical disability or health condition that may limit physical activity levels.\n* Schools participating in any other physical activity or health promotion program.",{"count":790,"type":21},800,[24],"Study based on a school-based physically active learning intervention during the school day on physical activity, fitness, health and education outcomes in adolescents.",[561,765,27],[795,770,771,772],"Physuca active learning","2024-09-06",{"date":775,"type":34},{"date":799,"type":34},"2024-09-02",{"date":801,"type":21},"2025-06-15",{"name":781,"class":41}]