[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"University of Oviedo\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":298},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,10,0,[8,49,79,105,130,157,182,211,241,273],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":20,"enrollmentInfo":21,"targetDuration":4,"studyType":24,"phases":25,"briefSummary":27,"conditions":28,"keywords":30,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":38,"lastUpdatePostDateStruct":39,"startDateStruct":42,"completionDateStruct":44,"leadSponsor":46,"locationsCount":4},"100630387","health-promotion-workshop-in-primary-school-children-100630387",false,"NCT07487012","Health Promotion Workshop in Primary School Children","Impact of a Health Promotion Workshop on Knowledge of Healthy Habits and Postural Hygiene in 3rd Grade Primary School Children","HEALTH-KIDS","Inclusion Criteria:\n\nStudents enrolled in 3rd grade of Primary Education at the participating school.\n\nAge between 8 and 9 years.\n\nWritten informed consent from parents or legal guardians.\n\nExclusion Criteria:\n\nPrevious participation in similar health education workshops during the current academic year.\n\nCognitive, sensory or communication difficulties that prevent understanding of the questionnaire.\n\nAbsence from school on the days of data collection.",true,"ALL","8 Years","9 Years",{"count":22,"type":23},40,"ESTIMATED","INTERVENTIONAL",[26],"NA","This study evaluates whether a brief educational workshop can improve knowledge of healthy habits and postural hygiene in primary school children.\n\nThe study will be conducted in 3rd grade students (8-9 years old) from a primary school in Spain. Children in the intervention group will attend a 45-minute health promotion workshop covering physical activity, correct posture in daily activities, backpack organization and basic musculoskeletal self-care. Children in the control group will not receive the workshop during the initial phase.\n\nAll participating students will complete a short knowledge questionnaire before and after the workshop period. The study aims to determine whether children who receive the workshop show greater improvement in knowledge compared to those who do not.\n\nParticipation is voluntary and requires written informed consent from parents or legal guardians. No medical procedures, treatments, access to medical records or biological samples are involved. Data will be coded and treated confidentially.",[29],"Health Education in Schoolchildren",[31,32,33,34,35,36],"School health promotion","Postural hygiene","Healthy habits","Primary school children","Educational intervention","Health knowledge","NOT_YET_RECRUITING","2026-03-20",{"date":40,"type":41},"2026-03-25","ACTUAL",{"date":43,"type":23},"2026-02",{"date":45,"type":23},"2026-04",{"name":47,"class":48},"University of Oviedo","OTHER",{"id":50,"slug":51,"hasResults":11,"nctId":52,"briefTitle":53,"officialTitle":54,"acronym":55,"eligibilityCriteria":56,"healthyVolunteers":17,"sex":57,"minAge":58,"maxAge":4,"enrollmentInfo":59,"targetDuration":4,"studyType":24,"phases":61,"briefSummary":62,"conditions":63,"keywords":65,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":72,"lastUpdatePostDateStruct":73,"startDateStruct":75,"completionDateStruct":76,"leadSponsor":78,"locationsCount":4},"100630386","educational-program-on-exercise-during-pregnancy-100630386","NCT07486999","Educational Program on Exercise During Pregnancy","Educational Intervention on Therapeutic Exercise During Pregnancy: A Pilot Randomized Controlled Trial","EDUPREG","Inclusion Criteria:\n\n* Pregnant women between 24 and 36 weeks of gestation\n* Age 18 years or older\n* Ability to understand Spanish\n* Low-risk pregnancy\n\nExclusion Criteria:\n\n* High-risk pregnancy\n* Medical contraindications to exercise during pregnancy\n* Inability to complete online questionnaires","FEMALE","18 Years",{"count":60,"type":23},30,[26],"This study aims to evaluate whether a short educational session about safe therapeutic exercise during pregnancy can improve knowledge, confidence, and physical activity levels in pregnant women.\n\nAlthough exercise during pregnancy is safe and beneficial, many women have doubts or lack information about how to exercise correctly. This can lead to low physical activity levels during pregnancy.\n\nIn this pilot randomized controlled trial, pregnant women attending primary care health centers will be invited to participate. After completing baseline questionnaires, participants will be randomly assigned to one of two groups. The control group will receive standard prenatal information provided during routine care. The experimental group will receive standard care plus a structured educational session about therapeutic exercise during pregnancy.\n\nParticipants will complete questionnaires measuring knowledge about exercise during pregnancy, confidence to exercise safely, and physical activity levels before the intervention and two weeks afterward.\n\nThe study is educational only. No mandatory physical exercise is required, and usual medical care will not be modified. The results will help determine whether brief educational interventions can support healthier lifestyles during pregnancy.",[64],"Pregnancy",[66,67,35,68,69,70,71],"Exercise during pregnancy","Therapeutic exercise","Self-efficacy","Physical activity","Prenatal care","Pilot randomized trial","2026-03-17",{"date":74,"type":41},"2026-03-23",{"date":43,"type":23},{"date":77,"type":23},"2026-05",{"name":47,"class":48},{"id":80,"slug":81,"hasResults":11,"nctId":82,"briefTitle":83,"officialTitle":84,"acronym":4,"eligibilityCriteria":85,"healthyVolunteers":11,"sex":57,"minAge":58,"maxAge":4,"enrollmentInfo":86,"targetDuration":4,"studyType":88,"phases":4,"briefSummary":89,"conditions":90,"keywords":92,"overallStatus":96,"whyStopped":4,"lastUpdateSubmitDate":97,"lastUpdatePostDateStruct":98,"startDateStruct":100,"completionDateStruct":101,"leadSponsor":103,"locationsCount":104},"100624371","physical-activity-fatigue-social-support-and-psychological-well-being-in-women-with-primary-hypothyroidism-100624371","NCT07408765","Physical Activity, Fatigue, Social Support, and Psychological Well-Being in Women With Primary Hypothyroidism","Physical Activity, Fatigue, Social Support, and Psychological Well-Being in Women With Primary Hypothyroidism: A Multicenter Observational Cohort Study","Inclusion Criteria:\n\n* Have a diagnosis of primary hypothyroidism (clinical or subclinical), established by a specialist in Endocrinology or Internal Medicine based on TSH and FT4 levels.\n* Female.\n* Are aged ≥18 years at the time of inclusion.\n* Have stable treatment for thyroid dysfunction (levothyroxine dose or other replacement regimen without relevant modifications) for at least the previous 3 months, or a stable clinical condition if treatment is not required.\n* Are able to ambulate independently in the community (with or without usual assistive devices), allowing participation in light to moderate physical activity.\n* Are able to understand and complete the questionnaires independently.\n* Have provided written informed consent\n\nExclusion Criteria:\n\n* Have a diagnosis of severe medical conditions that predominantly limit the ability to perform physical activity independently of hypothyroidism (e.g., advanced heart failure, severe chronic respiratory disease).\n* Have severe psychiatric disorders or significant cognitive impairment that hinder understanding of the information or reliable completion of the questionnaires.\n* Have undergone major surgery, severe trauma, or an acute medical condition that has substantially limited physical activity in the three months prior to assessment.\n* Are pregnant or in the immediate postpartum period, due to potential hormonal and functional interference with the study variables.\n* Are concurrently participating in a clinical trial or a structured physical exercise program.",{"count":87,"type":23},96,"OBSERVATIONAL","Background. Primary hypothyroidism, both clinical and subclinical, is frequently associated with persistent fatigue, reduced psychological well-being, and lower levels of physical activity in adult women. However, evidence integrating these psychosocial factors remains limited and methodologically heterogeneous.\n\nObjective. To analyze the association between physical activity and fatigue, social support, and psychological well-being in women with primary hypothyroidism; to compare these profiles between clinical and subclinical hypothyroidism; and to explore the moderating effect of social support and psychological well-being on the relationship between fatigue and physical activity.\n\nMethods. An observational, analytical, multicenter cohort study will be conducted including 96 adult women with primary hypothyroidism from the Principality of Asturias. Physical activity levels will be assessed using the International Physical Activity Questionnaire-Short Form (IPAQ-SF), while fatigue, social support, and psychological well-being will be measured using the Fatigue Severity Scale (FSS), the Medical Outcomes Study Social Support Survey (MOS-SSS), and the WHO-5 Well-Being Index, respectively. Confounding variables will include age, body mass index, type of hypothyroidism (clinical or subclinical), and time since diagnosis. Descriptive analyses, comparisons between clinical and subclinical groups, and multiple linear regression models will be performed.\n\nExpected results. The study is expected to identify physical activity levels within the sample and determine which psychosocial factors are independently associated with physical activity. Additionally, fatigue is anticipated to be negatively associated with physical activity, whereas social support and psychological well-being are expected to show positive associations and potential moderating effects.",[91],"Hypothyroidism Primary",[93,94,69,95],"Female","Hypothyroidism","Physiotherapy","RECRUITING","2026-02-16",{"date":99,"type":41},"2026-02-19",{"date":97,"type":41},{"date":102,"type":23},"2026-05-15",{"name":47,"class":48},1,{"id":106,"slug":107,"hasResults":11,"nctId":108,"briefTitle":109,"officialTitle":110,"acronym":4,"eligibilityCriteria":111,"healthyVolunteers":17,"sex":57,"minAge":58,"maxAge":4,"enrollmentInfo":112,"targetDuration":4,"studyType":88,"phases":4,"briefSummary":114,"conditions":115,"keywords":117,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":124,"lastUpdatePostDateStruct":125,"startDateStruct":127,"completionDateStruct":128,"leadSponsor":129,"locationsCount":104},"100624370","residual-athletic-identity-body-image-and-emotional-symptoms-in-retired-rhythmic-gymnasts-100624370","NCT07408752","Residual Athletic Identity, Body Image, and Emotional Symptoms in Retired Rhythmic Gymnasts","Residual Athletic Identity, Body Image, and Emotional Symptoms in Retired Rhythmic Gymnasts: A Cross-Sectional Observational Study","Inclusion Criteria:\n\n* Are aged ≥18 years.\n* Are female.\n* Have practiced rhythmic gymnastics during their competitive stage at any competitive level.\n* Are retired from competitive practice at the time of participation.\n* Are able to report the time elapsed since retirement and the type of retirement (voluntary or involuntary).\n* Agree to participate by providing informed consent and completing the online survey.\n\nExclusion Criteria:\n\n* Are not truly retired (i.e., maintain active competitive participation at the time of the study).\n* Have a time since retirement greater than 5 years.\n* Have incomplete questionnaires for variables essential to the analysis.\n* Provide clearly inconsistent or implausible responses in key variables (e.g., evident incompatibilities between age, age at initiation, and career duration) that preclude valid interpretation of the data.",{"count":113,"type":23},100,"Background. Rhythmic gymnastics is a sport characterized by high physical and aesthetic demands and typically early competitive retirement. In this context, athletic identity and body image play a central role during the athletic career and may be compromised after retirement, particularly in aesthetic disciplines. However, the relationship between these constructs in retired rhythmic gymnasts has been scarcely investigated.\n\nObjective. To analyze the relationship between athletic identity and body image in retired rhythmic gymnasts, in order to better understand the psychosocial factors influencing post-retirement adaptation.\n\nMethods. An observational, analytical, cross-sectional study will be conducted using a self-administered online survey targeting retired rhythmic gymnasts aged ≥18 years. The primary study variables will be positive body image and residual athletic identity. Additional independent and predictive variables will include sociodemographic characteristics and sport career-related factors (age, age at initiation in rhythmic gymnastics, duration of the athletic career, highest competitive level achieved, and satisfaction with the athletic career). A set of potential confounding or moderating variables will also be considered (time since retirement and type of sport retirement). Statistical analyses will include descriptive statistics, bivariate analyses, and multiple linear regression models adjusted for potential confounders.\n\nExpected results. An association between residual athletic identity and body image after sport retirement is expected, moderated by time since retirement and type of retirement, with implications for identifying profiles of greater vulnerability and informing the design of preventive interventions.",[116],"Retirement",[118,119,120,121,116,122,123],"Gymnastics","Athletes","Body Image","Identity, Self","Mental Health","Adaptation","2026-02-12",{"date":126,"type":41},"2026-02-17",{"date":124,"type":23},{"date":102,"type":23},{"name":47,"class":48},{"id":131,"slug":132,"hasResults":11,"nctId":133,"briefTitle":134,"officialTitle":135,"acronym":4,"eligibilityCriteria":136,"healthyVolunteers":11,"sex":18,"minAge":58,"maxAge":4,"enrollmentInfo":137,"targetDuration":4,"studyType":88,"phases":4,"briefSummary":139,"conditions":140,"keywords":142,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":150,"lastUpdatePostDateStruct":151,"startDateStruct":152,"completionDateStruct":154,"leadSponsor":156,"locationsCount":104},"100625188","clinical-and-psychosocial-factors-associated-with-physical-activity-level-in-adults-with-marfan-syndrome-100625188","NCT07419386","Clinical and Psychosocial Factors Associated With Physical Activity Level in Adults With Marfan Syndrome","Clinical and Psychosocial Factors Associated With Physical Activity Level in Adults With Marfan Syndrome: A Cross-Sectional Observational Study","Inclusion Criteria:\n\n* Adults (≥18 years).\n* A confirmed diagnosis of Marfan syndrome according to accepted clinical criteria used in routine follow-up.\n* Ability to understand and complete an online questionnaire in Spanish.\n* Access to the internet and an appropriate device to complete the survey.\n* Provision of informed consent to participate in the study.\n\nExclusion Criteria:\n\n* Patients with cognitive impairment or comprehension\u002Fliteracy difficulties that preclude valid completion of the questionnaires.\n* Who have experienced a major cardiovascular event or undergone recent cardiovascular\u002Faortic surgery that substantially limits physical activity during the most recent reference period (e.g., within the past 3 months).\n* With acute conditions or recent musculoskeletal injuries not attributable to Marfan syndrome that markedly restrict physical activity during the previous 7 days (the reference period of the IPAQ-SF).\n* With incomplete questionnaires for essential variables (IPAQ-SF and\u002For main predictors)",{"count":138,"type":23},118,"Background. Marfan syndrome is a genetic connective tissue disorder with cardiovascular and musculoskeletal involvement. Despite clinical advances, many patients exhibit low levels of physical activity, influenced by clinical and psychosocial factors such as fear of exertion, fatigue, or pain. Physical activity behavior in this population remains insufficiently characterized.\n\nObjective. To assess the level of physical activity in adults with Marfan syndrome and to identify the main associated clinical and psychosocial factors, in order to determine predictors of low physical activity.\n\nMethods. An observational, analytical, cross-sectional study will be conducted. Adults with a diagnosis of Marfan syndrome will be included. The primary outcome will be physical activity level, assessed using the International Physical Activity Questionnaire-Short Form. The main independent variables will include kinesiophobia (Tampa Scale for Kinesiophobia), physical activity self-efficacy, perceived fatigue (Fatigue Severity Scale), musculoskeletal pain (Brief Pain Inventory-Short Form), and cardiovascular clinical factors. Potential confounders will include age, sex, body mass index, time since diagnosis, medical recommendations regarding exercise, and current pain. Descriptive analyses and a multivariable logistic regression model will be performed to identify independent predictors of low physical activity.\n\nExpected results. To characterize the level of physical activity in adults with Marfan syndrome and to identify the clinical and psychosocial factors that independently predict low physical activity in this population.",[141],"Marfan Syndrome",[143,144,145,146,147,148,149],"Marfan syndrome","Motor activity","Exercise","Kinesiophobia","Fatigue","Pain","Self efficacy","2026-02-11",{"date":99,"type":41},{"date":153,"type":23},"2026-02-22",{"date":155,"type":23},"2026-05-26",{"name":47,"class":48},{"id":158,"slug":159,"hasResults":11,"nctId":160,"briefTitle":161,"officialTitle":162,"acronym":4,"eligibilityCriteria":163,"healthyVolunteers":11,"sex":18,"minAge":58,"maxAge":164,"enrollmentInfo":165,"targetDuration":167,"studyType":88,"phases":4,"briefSummary":168,"conditions":169,"keywords":171,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":174,"lastUpdatePostDateStruct":175,"startDateStruct":177,"completionDateStruct":179,"leadSponsor":181,"locationsCount":104},"100586736","physical-activity-in-patients-with-systemic-lupus-erythematosus-100586736","NCT06919250","Physical Activity in Patients With Systemic Lupus Erythematosus","Physical Activity and Its Impact on Health in Patients With Systemic Lupus Erythematosus. A Multicenter Cohort Study.","Inclusion Criteria:\n\n* Patients with a diagnosis of systemic lupus erythematosus\n* Of legal age\n* Residents in Spain\n* Who sign the informed consent document.\n\nExclusion Criteria:\n\n* Patients dependent in the development of activities of daily living.\n* Unable to ambulate without the help of third parties.\n* Who have undergone surgery in the last 6 months.","65 Years",{"count":166,"type":23},63,"1 Day","Background. Systemic lupus erythematosus is a chronic autoimmune disease. Among its main clinical manifestations are musculoskeletal symptoms such as myopathies, arthritis, arthralgias or osteonecrosis. Physical activity can improve the perception of quality of life and well-being of these patients.\n\nObjective. To assess the degree of physical activity in patients with systemic lupus erythematosus, and to identify the main clinical, sociodemographic and anthropometric variables that influence it.\n\nMethod. Ambispective cohort study. Sixty-three patients with systemic lupus erythematosus will be recruited. The primary variable will be the degree of physical activity (International Physical Activity Questionnaire). Secondary and modifying variables will be: fatigue (Fatigue Assessment Scale), health-related quality of life (Short Form-36 Health Survey), sleep disorders (Pittsburgh Sleep Quality Index), depressive (Beck Depression Inventory -II) and anxiety symptoms (Hamilton Anxiety Rating Scale), age, and disease activity, duration and damage. Possible confounding variables will be sex, toxic habits (smoking), diagnosis of other pathologies and exposure to therapy. In the analysis, the degree of physical activity of patients with lupus erythematosus will be calculated and a multiple regression analysis will be performed to evaluate the predictive model that best fits the degree of activity of these patients.\n\nExpectedresults. To identify the degree of physical activity of patients with systemic lupus erythematosus and to identify the predictive model of physical activity in these patients.",[170],"Lupus Erythematosus, Systemic",[172,69,173,95],"Systemic Lupus Erythematosus","Prevention","2025-04-04",{"date":176,"type":41},"2025-04-09",{"date":178,"type":23},"2025-03-31",{"date":180,"type":23},"2025-05-20",{"name":47,"class":48},{"id":183,"slug":184,"hasResults":11,"nctId":185,"briefTitle":186,"officialTitle":187,"acronym":188,"eligibilityCriteria":189,"healthyVolunteers":11,"sex":18,"minAge":4,"maxAge":4,"enrollmentInfo":190,"targetDuration":4,"studyType":88,"phases":4,"briefSummary":192,"conditions":193,"keywords":195,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":203,"lastUpdatePostDateStruct":204,"startDateStruct":206,"completionDateStruct":208,"leadSponsor":210,"locationsCount":4},"100579379","prevalence-of-temporomandibular-joint-disorders-in-wind-musicians-100579379","NCT06823531","Prevalence of Temporomandibular Joint Disorders in Wind Musicians","Prevalence of Temporomandibular Joint Disorders in Wind Musicians and Their Relationship with Instrument Type","TMD-WIND","Inclusion Criteria:\n\n* Wind musicians (professional or student).\n* Any age (if under 18, parental\u002Flegal guardian consent is required).\n* Signed informed consent.\n\nExclusion Criteria:\n\n* History of maxillofacial surgery.\n* Presence of neurological disorders affecting mandibular function.\n* Recent treatment for TMD.\n* Severe bruxism diagnosis.",{"count":191,"type":23},50,"This study aims to analyze the prevalence of temporomandibular joint disorders (TMD) in wind musicians, differentiating the impact by instrument type (woodwind vs. brass) and identifying potential risk factors (embouchure, posture, practice time). A cross-sectional observational design will be used, including professional and student musicians from orchestras and conservatories.",[194],"Temporomandibular Disorders (TMD)",[196,197,198,199,200,201,202],"Temporomandibular disorders","TMD","Orofacial pain","Embouchure Disorders","Bruxism","Mandibular Mobility","Jaw diseases","2025-03-09",{"date":205,"type":41},"2025-03-11",{"date":207,"type":23},"2025-03-15",{"date":209,"type":23},"2025-04-15",{"name":47,"class":48},{"id":212,"slug":213,"hasResults":11,"nctId":214,"briefTitle":215,"officialTitle":216,"acronym":217,"eligibilityCriteria":218,"healthyVolunteers":17,"sex":18,"minAge":58,"maxAge":4,"enrollmentInfo":219,"targetDuration":4,"studyType":24,"phases":220,"briefSummary":221,"conditions":222,"keywords":228,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":203,"lastUpdatePostDateStruct":235,"startDateStruct":237,"completionDateStruct":238,"leadSponsor":240,"locationsCount":104},"100578748","efficacy-of-shock-wave-therapy-in-post-stroke-muscle-spasticity-management-100578748","NCT06815328","Efficacy of Shock Wave Therapy in Post-Stroke Muscle Spasticity Management","Efficacy of Shock Wave Therapy in Patients with Muscle Spasticity After a Stroke","SWT-PI","\"Inclusion Criteria\":\n\n* Adults aged 18 years or older.\n* Confirmed diagnosis of stroke (ischemic or hemorrhagic) at least 6 months prior to enrollment.\n* Clinically diagnosed muscle spasticity, measured by the Modified Ashworth Scale (MAS), with a score of 0 to 3.\n* Stable medical condition that permits participation in the intervention.\n* No significant changes in spasticity-related treatment for at least 3 months prior to the study.\n* Ability to provide written informed consent to participate in the study.\n* Ability to attend weekly sessions and follow-up visits as required.\n\n\"Exclusion Criteria\":\n\n* Severe spasticity or contractures unresponsive to prior treatments.\n* Contraindications to Shock Wave Therapy, including:\n* Local infections in the treatment area.\n* Known or suspected malignancy near the treatment site.\n* Severe bleeding disorders or anticoagulation therapy.\n* Pregnancy.\n* Neurological conditions other than stroke that could interfere with study outcomes (e.g., Parkinson's disease, multiple sclerosis).\n* Recent treatments that might interfere with spasticity assessment, including:\n* Injections of botulinum toxin within the past 6 months.\n* Recent surgery or other interventions targeting spasticity.\n* Cognitive impairment or other conditions preventing the participant from following instructions or completing study tasks.\n* Severe cardiovascular, renal, or hepatic disease that might complicate therapy or participation.\n* Inability to commit to follow-up visits or complete the intervention protocol due to logistical, mobility, or health-related issues.",{"count":191,"type":23},[26],"The goal of this clinical trial is to evaluate the efficacy and safety of shock wave therapy (SWT) in reducing muscle spasticity in patients who have suffered a stroke. The main questions it aims to answer are:\n\nDoes SWT reduce muscle tone and improve joint range of motion in post-stroke patients with spasticity? Does SWT improve the quality of life for these patients? What side effects, if any, occur during or after SWT? Researchers will compare SWT to conventional spasticity treatments to determine its effectiveness and potential advantages.\n\nParticipants will:\n\nUndergo SWT sessions as part of their rehabilitation protocol over a period of 8 weeks.\n\nAttend follow-up visits to assess muscle tone, joint mobility, and overall functional improvement.\n\nComplete quality-of-life questionnaires to measure the therapy's impact on daily living.",[223,224,225,226,227,95],"Stroke","Spasticity","Post-stroke","Muscle Hypertonia","Neurological Disorders",[229,230,231,232,233,234],"Shock Wave Therapy","Post-Stroke Spasticity","Non-Invasive Therapy","Quality of Life","Neurological physical therapy","Muscle Hypertonia Treatment",{"date":236,"type":41},"2025-03-12",{"date":207,"type":23},{"date":239,"type":23},"2025-04-30",{"name":47,"class":48},{"id":242,"slug":243,"hasResults":11,"nctId":244,"briefTitle":245,"officialTitle":246,"acronym":247,"eligibilityCriteria":248,"healthyVolunteers":17,"sex":18,"minAge":58,"maxAge":4,"enrollmentInfo":249,"targetDuration":4,"studyType":88,"phases":4,"briefSummary":251,"conditions":252,"keywords":257,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":265,"lastUpdatePostDateStruct":266,"startDateStruct":268,"completionDateStruct":270,"leadSponsor":272,"locationsCount":4},"100581309","impact-of-equestrian-sports-crossfit-and-gym-training-on-pelvic-floor-health-pelfisport--100581309","NCT06848634","Impact of Equestrian Sports, CrossFit, and Gym Training on Pelvic Floor Health (PELFISPORT )","Impact of Equestrian Sports, CrossFit, and Gym Training on Pelvic Floor Health in Athletes and Non-Athletes: A Cross-Sectional Study","PELFISPORT","Inclusion Criteria:\n\n* Adults 18 years or older.\n* Voluntary participation with signed informed consent.\n* Completion of the online survey.\n* For the sports groups (Equestrian, CrossFit, Gym, Other Sports):\n\n  * Minimum 2 years of experience in the sport.\n  * Minimum 2 training sessions per week.\n\nExclusion Criteria:\n\n* Individuals under 18 years old.\n* Participants who do not complete the survey.\n* Individuals with neurological conditions affecting mobility.\n* Individuals with mobility impairments unrelated to sports.\n* Sports participants with less than 2 years of experience or training less than twice per week.",{"count":250,"type":23},200,"This observational cross-sectional study investigates the impact of equestrian sports, CrossFit, and gym training on pelvic floor health in both athletes and non-athletes. The study aims to determine whether specific sports are associated with a higher risk of pelvic floor dysfunction, including urinary incontinence, pelvic organ prolapse, and chronic pelvic pain.\n\nParticipants will complete an online survey that collects demographic information, sports participation details, and pelvic floor health symptoms. The survey includes standardized questionnaires to assess pelvic floor function. Data will be analyzed to compare the prevalence of pelvic floor issues among different sports and between athletes and non-athletes.\n\nThe study seeks to provide insights into how sports participation influences pelvic health and to raise awareness of pelvic floor dysfunction in both male and female athletes.",[253,254,255,256],"Pelvic Floor Dysfunction","Urinary Incontinence","Pelvic Organ Prolapse (POP)","Chronic Pelvic Pain",[258,259,260,261,262,263,264,69],"Urinary incontinence","Pelvic organ prolapse","Chronic pelvic pain","Equestrian sports","CrossFit","Gym training","Women's health","2025-02-26",{"date":267,"type":41},"2025-02-27",{"date":269,"type":23},"2025-02-28",{"date":271,"type":23},"2025-04-05",{"name":47,"class":48},{"id":274,"slug":275,"hasResults":11,"nctId":276,"briefTitle":277,"officialTitle":277,"acronym":4,"eligibilityCriteria":278,"healthyVolunteers":11,"sex":18,"minAge":58,"maxAge":4,"enrollmentInfo":279,"targetDuration":4,"studyType":24,"phases":281,"briefSummary":282,"conditions":283,"keywords":286,"overallStatus":96,"whyStopped":4,"lastUpdateSubmitDate":290,"lastUpdatePostDateStruct":291,"startDateStruct":293,"completionDateStruct":295,"leadSponsor":297,"locationsCount":104},"100564460","cognitive-behavioral-treatment-with-activity-trackers-for-smoking-cessation-100564460","NCT06629467","Cognitive Behavioral Treatment with Activity Trackers for Smoking Cessation","Inclusion Criteria:\n\n* Being aged 18 or over.\n* Smoking at least 10 cigarettes per day.\n\nExclusion Criteria:\n\n* Being currently receiving other psychological or pharmacological treatment for smoking cessation.\n* Being diagnosed with substance use disorder or severe psychiatric disorder.\n* Active suicidal ideation.",{"count":280,"type":23},128,[26],"Given the high prevalence of deaths per year attributable to tobacco use, improving smoking cessation treatments is an important public health priority Worldwide. It is also known that practicing physical activity (PA) may help smoking cessation. Physical activity trackers have been demonstrated to increase PA levels in different studies with various populations, as a sole intervention or in combination with interventions targeting PA.\n\nThis study aims to examine the feasibility, effect, and cost-effectiveness of cognitive-behavioral therapy (CBT) + Personalized physical activity (PA) + Physical Activity Tracker use (Fitbit Versa 3®) for smoking cessation. Given the high prevalence of deaths per year attributable to tobacco use, improving smoking cessation treatments is an important public health priority worldwide.\n\nIn this study, an estimated sample of 128 adult smokers will be randomly allocated to one of the following conditions: 1) CBT for smoking cessation + personalized PA plan + Fitbit Versa 3®; 2) CBT for smoking cessation + personalized PA plan.\n\nMail goals: 1) To examine the feasibility (i.e., adherence, perceived utility, satisfaction) of integrating Fitbit Versa 3® into a CBT protocol for smoking cessation; 2) to examine the effectiveness of CBT for smoking cessation + personalized PA plan + Fitbit Versa 3® and CBT for smoking cessation + personalized PA plan in terms of smoking abstinence rates (point-prevalence and days of continuous abstinence), PA (i.e., steps per day, moderate to vigorous physical activity) and mental health outcomes (anxiety and depression symptoms, emotional dysregulation); 3) to examine the cost-effectiveness of CBT for smoking cessation + personalized PA plan + Fitbit Versa 3® vs. CBT for smoking cessation + personalized PA plan in terms of smoking abstinence rates (point-prevalence and days of continuous abstinence), PA (i.e., steps per day, moderate to vigorous physical activity) and mental health outcomes (anxiety and depression symptoms, emotional dysregulation).",[284,285],"Tobacco Use Cessation","Physical Activity",[287,69,288,289],"Tobacco","Activity tracker","Cognitive-behavioral therapy","2024-10-04",{"date":292,"type":41},"2024-10-08",{"date":294,"type":41},"2023-05-10",{"date":296,"type":23},"2025-12-01",{"name":47,"class":48},""]