[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"performance\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:performance":31},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,14,0,[8,54,82,93,129,164,191,218,252,281,308,334,361,392],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":4,"enrollmentInfo":20,"targetDuration":23,"studyType":24,"phases":4,"briefSummary":25,"conditions":26,"keywords":33,"overallStatus":41,"whyStopped":4,"lastUpdateSubmitDate":42,"lastUpdatePostDateStruct":43,"startDateStruct":46,"completionDateStruct":48,"leadSponsor":50,"locationsCount":53},"100054043","intraoperative-cognitive-load-in-anesthesia-nurses-across-anesthetic-phases-100054043",false,"NCT07568158","Intraoperative Cognitive Load in Anesthesia Nurses Across Anesthetic Phases","Carga Cognitiva Intraoperatoria Del Enfermero\u002Fa de Anestesia Según la Fase Del Acto Anestésico: Estudio Observacional Con NASA-TLX","ENCOPER","Inclusion Criteria:\n\n* Registered nurse anesthetist actively working at Hospital Clínic de Barcelona.\n* Minimum 3 months in the current anesthesia nursing position.\n* Voluntary participation with signed informed consent.\n* Scheduled surgery (including deferred urgent surgery) or solid organ transplantation.\n* General anesthesia (endotracheal intubation or laryngeal mask airway) or spinal anesthesia with sedation.\n* Minimum duration of 30 minutes.\n\nExclusion Criteria:\n\n* Refusal to participate or withdrawal of informed consent.\n* Spinal anesthesia without sedation.\n* Exclusive regional anesthesia without sedation.\n* Sedation alone without regional technique.\n* Duration less than 30 minutes.\n* Cases involving an unexpected intraoperative emergency requiring urgent additional personnel.\n* Cases started under spinal anesthesia converted to general anesthesia for any clinical or technical reason.",true,"ALL","18 Years",{"count":21,"type":22},50,"ESTIMATED","8 Months","OBSERVATIONAL","The goal of this observational study is to measure the cognitive load (mental effort) of anesthesia nurses during real surgical procedures at Hospital Clínic de Barcelona, Spain. The main questions it aims to answer are:\n\n* Does cognitive load vary across the three phases of anesthetic care (induction, maintenance, and emergence\u002Frecovery)?\n* Is cognitive load higher during general anesthesia than during spinal anesthesia with sedation?\n* How do surgical specialty and patient complexity relate to cognitive load?\n* How does monitor alarm perception relate to cognitive load during surgery?\n\nParticipants (anesthesia nurses) will complete the NASA Task Load Index (NASA-TLX) questionnaire - a validated 6-item tool measuring mental effort - three times per surgical case: after induction or spinal block, during maintenance, and after patient awakening or sedation reversal. They will also answer 4 brief questions about alarm management at the end of each case. No changes are made to clinical care. Participation adds approximately 11 minutes per surgical case.",[27,28,29,30,31,32],"Alarm Fatigue","Perioperative","Patient Safety","Cognitive Load","Performance","Cognitive Load, Performance",[34,35,36,37,38,29,39,40],"NASA-TLX","Anesthesia Nursing","Perioperative Nursing","Mental Workload","Intraoperative","Monitor Alarms","Operating Room","RECRUITING","2026-07-10",{"date":44,"type":45},"2026-07-13","ACTUAL",{"date":47,"type":45},"2026-06-01",{"date":49,"type":22},"2027-02-28",{"name":51,"class":52},"Hospital Clinic of Barcelona","OTHER",1,{"id":55,"slug":56,"hasResults":11,"nctId":57,"briefTitle":58,"officialTitle":58,"acronym":59,"eligibilityCriteria":60,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":61,"enrollmentInfo":62,"targetDuration":4,"studyType":63,"phases":64,"briefSummary":66,"conditions":67,"keywords":70,"overallStatus":73,"whyStopped":4,"lastUpdateSubmitDate":74,"lastUpdatePostDateStruct":75,"startDateStruct":77,"completionDateStruct":78,"leadSponsor":80,"locationsCount":53},"100642275","the-role-of-carbohydrate-blends-and-electrolytes-on-physical-and-mental-performance-during-cycling-in-the-heat-100642275","NCT07658820","The Role of Carbohydrate Blends and Electrolytes on Physical and Mental Performance During Cycling in the Heat","CARB-HEAT","Inclusion Criteria:\n\n* Healthy and injury free (muscle, skeletal) for greater than 2 months\n* Active cyclists who train at least 3 times per week\n* Body mass index (BMI) range of 18.5-30 kg\u002Fm2\n* VO₂max ≥ 51 mL\u002Fkg\u002Fmin for male participants\n* VO₂max ≥ 45 mL\u002Fkg\u002Fmin for female participants\n\nExclusion Criteria:\n\n* Taking medicine influences the cardiovascular system\n* non-steroidal anti-inflammatory drugs during the last week\n* Cancer Diagnosis during the last 5 years\n* Current Pregnancy\n* History of renal disease, hypertension, obstructive gastrointestinal tract disease, disorders or impairment of the gag reflex, previous gastrointestinal surgery\n* History of heat stroke\n* Use of testosterone therapy\n* Adults who are unable to consent (impaired decision-making capacity)\n* Adults having Felinization of the esophagus\n* Adults who will undergo Nuclear Magnetic Resonance (NMR) or MRI scanning within 3 days of swallowing a temperature sensitive pills","55 Years",{"count":5,"type":22},"INTERVENTIONAL",[65],"NA","The aim of the present study is to evaluate the effectiveness of a milk permeate-based sports drink on hydration, carbohydrate oxidation, exercise performance, vigilance, and reaction time in the heat. We anticipate that the milk permeate, with 44 g per liter and high sodium and potassium, will lead to better hydration, energy delivery, and physical and cognitive performance.",[68,69,31],"Hydration","Dehydration (Physiology)",[71,72],"exercise in the heat","cognitive performance","NOT_YET_RECRUITING","2026-06-17",{"date":76,"type":45},"2026-06-22",{"date":76,"type":22},{"date":79,"type":22},"2027-12-31",{"name":81,"class":52},"Arizona State University",{"id":83,"slug":4,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":4,"enrollmentInfo":84,"targetDuration":23,"studyType":24,"phases":4,"briefSummary":25,"conditions":85,"keywords":86,"overallStatus":41,"whyStopped":4,"lastUpdateSubmitDate":87,"lastUpdatePostDateStruct":88,"startDateStruct":89,"completionDateStruct":90,"leadSponsor":92,"locationsCount":53},"100636628",{"count":21,"type":22},[27,28,29,30,31,32],[34,35,36,37,38,29,39,40],"2026-06-15",{"date":74,"type":45},{"date":47,"type":45},{"date":91,"type":22},"2027-01-01",{"name":51,"class":52},{"id":94,"slug":95,"hasResults":11,"nctId":96,"briefTitle":97,"officialTitle":97,"acronym":4,"eligibilityCriteria":98,"healthyVolunteers":17,"sex":99,"minAge":19,"maxAge":100,"enrollmentInfo":101,"targetDuration":4,"studyType":63,"phases":103,"briefSummary":104,"conditions":105,"keywords":112,"overallStatus":41,"whyStopped":4,"lastUpdateSubmitDate":120,"lastUpdatePostDateStruct":121,"startDateStruct":123,"completionDateStruct":125,"leadSponsor":127,"locationsCount":53},"100638291","effects-of-carbon-fiber-insoles-on-cmj-and-sprint-performance-100638291","NCT07589231","Effects of Carbon Fiber Insoles on CMJ and Sprint Performance","Inclusion Criteria:\n\n* Men aged 18-30 years\n* Moderate physical activity (2-4 times\u002Fweek)\n* No injuries in the last 6 months\n\nExclusion Criteria:\n\n* Use of orthoses or podiatric pathologies\n* Neurological or cardiovascular disease\n* Refusal to sign informed consent","MALE","30 Years",{"count":102,"type":22},38,[65],"This study evaluates the effects of VKTRY carbon fiber insoles on vertical jump and sprint performance in moderately active men. Participants will perform tests with and without insoles, assessing both objective performance and subjective perception using a Likert-type scale.",[106,107,108,31,109,110,111],"Healthy","Sportsman","Prevention","Healthy Adult Man","Sports Performance","Athletic Performance and Injury Risk",[113,114,115,116,117,118,119],"sprint","insoles","carbon fiber insoles","vertical jump","biomechanics","sports performance","my jump lab","2026-05-13",{"date":122,"type":45},"2026-05-15",{"date":124,"type":45},"2025-10-30",{"date":126,"type":22},"2026-06-30",{"name":128,"class":52},"Benjamín Cuenca Valero",{"id":130,"slug":131,"hasResults":11,"nctId":132,"briefTitle":133,"officialTitle":134,"acronym":135,"eligibilityCriteria":136,"healthyVolunteers":17,"sex":99,"minAge":19,"maxAge":137,"enrollmentInfo":138,"targetDuration":4,"studyType":63,"phases":140,"briefSummary":141,"conditions":142,"keywords":148,"overallStatus":73,"whyStopped":4,"lastUpdateSubmitDate":156,"lastUpdatePostDateStruct":157,"startDateStruct":158,"completionDateStruct":160,"leadSponsor":162,"locationsCount":53},"100640496","acute-effects-of-exercise-bars-on-proprioception-reactiontime-power-and-upper-extremity-performance-100640496","NCT07574788","Acute Effects of Exercise Bars on Proprioception, ReactionTime, Power and Upper Extremity Performance","The Effect of Acutely Applied Exercise Bars on Proprioception, Reaction Time, Power and Upper Extremity Performance","EXBAR-RT","Inclusion Criteria:\n\n* Aged between 18 and 35 years\n* Healthy individuals\n* No history of upper extremity injury\n* No neurological disorders\n* Voluntary participation\n\nExclusion Criteria:\n\n* Presence of any neurological disease\n* History of upper extremity surgery\n* Current musculoskeletal pain or injury\n* Any condition affecting proprioception or reaction time\n* Inability to comply with study procedures","35 Years",{"count":139,"type":22},45,[65],"This study will be conducted between May and August 2026 at Aydın Adnan Menderes University, Faculty of Health Sciences, with male individuals aged 18-35. For the study, cases will first be divided into 3 groups by computer-assisted randomization.The first group will be the Flex-i bar group, the second group will be the Theraband Flex bar group, and the third group will be the Sham bar group. Group 1 will perform the exercises with the Flex-i bar, while Group 2 will perform them with the Theraband Flex bar. The control group will perform the exercises with a rolling pin.After group assignment of cases is completed, demographic information such as age, height and weight of the participants will be recorded. Then, pre-exercise assessments of the participants will be conducted. The assessment will include proprioception, reaction time, power and upper extremity performance. Following the initial assessment, each group will perform their exercises with their own exercise material. Measurements will be repeated after the exercises. Measurements will be taken three times during the assessments and the best result will be recorded.",[143,144,145,31,146,147],"Reaction Time","Proprioception","Power","Athletic Performance","Flexi-bar",[149,150,151,152,153,154,155],"reaction time","proprioception","power","performance tests","performance","exercise bars","acute effect","2026-05-10",{"date":120,"type":45},{"date":159,"type":22},"2026-05-01",{"date":161,"type":22},"2026-08-01",{"name":163,"class":52},"Aydin Adnan Menderes University",{"id":165,"slug":166,"hasResults":11,"nctId":167,"briefTitle":168,"officialTitle":169,"acronym":4,"eligibilityCriteria":170,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":4,"enrollmentInfo":171,"targetDuration":4,"studyType":63,"phases":173,"briefSummary":174,"conditions":175,"keywords":179,"overallStatus":73,"whyStopped":4,"lastUpdateSubmitDate":182,"lastUpdatePostDateStruct":183,"startDateStruct":185,"completionDateStruct":187,"leadSponsor":189,"locationsCount":53},"100624268","eeg-guided-binaural-beat-audio-to-reduce-performance-related-stress-and-improve-cognition-100624268","NCT07407426","EEG-Guided Binaural Beat Audio to Reduce Performance-Related Stress and Improve Cognition","Effects of EEG-guided Binaural Beat Audio Intervention on Brain Reactivity Associated With Performance-related Stress and Cognition Among Professional Musicians: A Randomized, Double-blinded, Sham-controlled Functional Neuroimaging Trial","Inclusion Criteria:\n\n* Adults (18+ years) enrolled as undergraduate music majors at Texas Tech University\n* Currently preparing for an upcoming concert performance within the next 3 months\n* Able to read standard musical notation\n\nExclusion Criteria:\n\n* Subjects with contraindications to undergo MRI after being screened by the TTNI safety screening sheet - specifically, Subjects with implanted devices that are not compatible with MRI including, but not limited to cardiac pacemakers, cardiac defibrillators, aneurysm clips, carotid artery vascular clamps, implanted nerve stimulators (neuron-stimulators also called TENS or wires), bone growth or bone fusion stimulators, cochlear implants, vagus nerve stimulators, filters for blood clots (Umbrella, Greenfield, bird's nest), embolization coils (e.g. Gianturco) in the brain, ocular implants, vascular stents, medication pumps, medication patches delivering medications, implanted limbs, ventricular shunts, metal joints, rods, plates, pins, screws, nails, or clips, penile implants, or contraceptives devices including IUDs, cervical pessaries and diaphragms Subjects who have undergone cataract surgery Subjects who have shrapnel or metal in the head, eyes or skin Subjects with a history of working with metal fragments ( or have had metal removed from eyes Subjects with gunshot wounds or BB gun injury Subjects with permanent metal body piercings or jewelry that cannot be removed Subjects who use hearing aids or have braces \u002F permanent retainers that cannot be removed temporarily for the MRI scans Subjects with large tattoos in the head and neck area Subjects with claustrophobia Subjects who are currently pregnant or suspected to be pregnant\n* Physical, medical, neurological or psychiatric impairments (including substance abuse)\n* Current use of medications that could affect cognitive performance (including beta-blockers, stimulants, anxiolytics, antidepressants, or antipsychotics)\n* History of head injury resulting in loss of consciousness\u002Fhistory of brain surgery\n* History of diagnosed hearing impairment or use of hearing aids\n* Current or past diagnosis of epilepsy or seizure disorders\n* Unwillingness or inability to refrain from alcohol consumption 48 hours prior to the study visit\n* Unwillingness or inability to refrain from caffeine consumption 12 hours prior to the study visit\n* Current\u002Fpast history of substance abuse\n* Pregnancy or possibility of pregnancy\n* Unwillingness or inability to follow written, on-screen, and verbal instructions given by the study team",{"count":172,"type":22},32,[65],"Performance-related stress can impair sustained attention, inhibitory control, and memory. This randomized, double-blinded, sham-controlled parallel-arm trial evaluates whether a 30-minute EEG-guided binaural beat audio intervention reduces subjective stress\u002Fperformance anxiety and improves cognition, and whether it changes task-related brain reactivity measured by fMRI. The intervention uses real-time single-electrode EEG recorded over the left prefrontal cortex to dynamically adjust binaural beat frequencies to guide the brain toward a target state; the sham condition uses non-binaural music delivered through identical headphones.\n\nAdult music majors preparing for an upcoming concert will complete pre- and post-intervention fMRI sessions during cognitive\u002Fmusic tasks (Stop Signal Reaction Task, Music Reading Task, Music Memory Retrieval Task) and complete visual analog scales (VAS) assessing performance anxiety, stress, and related subjective states. The primary outcomes include fMRI task-related activity in stress-regulation regions (dlPFC, amygdala, hippocampus), behavioral inhibition indices from the stop-signal task, music memory retrieval accuracy, and VAS-reported stress\u002Fperformance anxiety.",[176,31,177,178],"Cognitive Abilities","Stress","Cognitive Performance",[180,72,181],"neurofeedback","stress","2026-04-06",{"date":184,"type":45},"2026-04-13",{"date":186,"type":22},"2026-04-07",{"date":188,"type":22},"2026-08-30",{"name":190,"class":52},"Texas Tech University Health Sciences Center",{"id":192,"slug":193,"hasResults":11,"nctId":194,"briefTitle":195,"officialTitle":195,"acronym":196,"eligibilityCriteria":197,"healthyVolunteers":17,"sex":18,"minAge":198,"maxAge":19,"enrollmentInfo":199,"targetDuration":4,"studyType":63,"phases":201,"briefSummary":202,"conditions":203,"keywords":207,"overallStatus":73,"whyStopped":4,"lastUpdateSubmitDate":211,"lastUpdatePostDateStruct":212,"startDateStruct":214,"completionDateStruct":215,"leadSponsor":216,"locationsCount":53},"100629584","clinical-trial-of-lactiplantibacillus-plantarum-dad-13-on-gut-microbiota-profile-and-performance-in-adolescent-athletes-100629584","NCT07476573","Clinical Trial of Lactiplantibacillus Plantarum Dad-13 on Gut Microbiota Profile and Performance in Adolescent Athletes","Dad-13","Inclusion Criteria:\n\n* Residing in the BPPLOP dormitory of Central Java Province;\n* Having a normal body mass index;\n* Being an athlete in an endurance sport;\n* Having no growth disorders\n\nExclusion Criteria:\n\n* Injury, any health contraindication or failure to perform exercise procedures;\n* Gastrointestinal infections, diseases, disorders;\n* Past history of gastrointestinal surgery;\n* Failure to follow the study protocol;\n* Declared general feeling of being unwell","12 Years",{"count":200,"type":22},30,[65],"The aim of this research is to analyze the effect of a Lactiplantibacillus plantarum Dad-13 supplementation on the gut microbiota profile and performance of adolescent athletes.",[204,205,31,206],"Athlete","Probiotic","Gut Microbiota",[208,209,153,210],"athlete","probiotic","gut microbiota","2026-03-19",{"date":213,"type":45},"2026-03-23",{"date":184,"type":22},{"date":188,"type":22},{"name":217,"class":52},"Gadjah Mada University",{"id":219,"slug":220,"hasResults":11,"nctId":221,"briefTitle":222,"officialTitle":223,"acronym":224,"eligibilityCriteria":225,"healthyVolunteers":17,"sex":226,"minAge":4,"maxAge":4,"enrollmentInfo":227,"targetDuration":229,"studyType":24,"phases":4,"briefSummary":230,"conditions":231,"keywords":239,"overallStatus":73,"whyStopped":4,"lastUpdateSubmitDate":243,"lastUpdatePostDateStruct":244,"startDateStruct":246,"completionDateStruct":248,"leadSponsor":250,"locationsCount":4},"100622850","magia-h3s-point-of-care-test-performance-for-hiv-hbv-hcv-and-syphilis-screening-in-pregnant-women-in-dr-congo-100622850","NCT07388979","MAGIA H3S Point of Care Test Performance for HIV, HBV, HCV, and Syphilis Screening in Pregnant Women in DR Congo","MAGIa In-vitro- Diagnostics Medical Device Dedicated to Combined Screening of HIV, HBV, HCV and Syphilis and HBV Reflective Panels aMong Congolese pregnAnt woMen Attending to Ante Natal Care Consultations","MAGICS MAM","Inclusion Criteria:\n\n* Being pregnant, regardless of age or stage of pregnancy (prenatal period);\n* Having signed an informed consent form at the start of prenatal care (CPN) to participate in the study.\n\nNote: for pregnant minors, the consent of a parent or legal guardian is required;\n\n* Have chosen to attend prenatal care at the healthcare facility selected for the study;\n* Plan to give birth at the same healthcare facility where they were included in the study;\n* Plan to attend postnatal care (PNC) and preschool consultations (PSC) at the same healthcare facility where they were included in the study.\n* Plan to give birth at the same health facility where they were enrolled;\n* Plan to attend postnatal consultations (PNC) and preschool consultations (PSC) at the same facility\n\nExclusion Criteria:\n\n* Women in labor or who refuse to give their consent.","FEMALE",{"count":228,"type":22},7500,"12 Months","Performance study to evaluate the clinical performance of the In-Vitro Diagnostic Medical Device MagIA H3S (a Multiplex Point-of-Care test for the combined detection of Human Immunodeficiency Virus (HIV), Hepatitis B and C and Syphilis) from pregnant women attending antenatal care (ANC) services in the Democratic Republic of the Congo. This study aligns with the WHO 2022-2030 strategy for the integrated elimination of mother-to-child transmission of HIV, HBV, HCV, and syphilis.",[232,233,234,235,236,31,237,238],"HIV - Human Immunodeficiency Virus","HBV (Hepatitis B Virus)","Hepatitis C Virus (HCV)","Syphilis","Mother-to-Child Transmission","Point of Care STI Testing","TREAT B",[240,241,242],"Triple elimination","Mother-to-child transmission","Democratic republic of the Congo","2026-01-28",{"date":245,"type":45},"2026-02-05",{"date":247,"type":22},"2026-03-01",{"date":249,"type":22},"2027-12-21",{"name":251,"class":52},"Gardiens de Vies",{"id":253,"slug":254,"hasResults":11,"nctId":255,"briefTitle":256,"officialTitle":257,"acronym":258,"eligibilityCriteria":259,"healthyVolunteers":17,"sex":99,"minAge":19,"maxAge":260,"enrollmentInfo":261,"targetDuration":4,"studyType":63,"phases":263,"briefSummary":264,"conditions":265,"keywords":267,"overallStatus":73,"whyStopped":4,"lastUpdateSubmitDate":272,"lastUpdatePostDateStruct":273,"startDateStruct":275,"completionDateStruct":277,"leadSponsor":279,"locationsCount":53},"100618096","bfr-rope-training-in-male-volleyball-players-100618096","NCT07327177","BFR Rope Training in Male Volleyball Players","The Effects of Blood Flow Restriction Rope Training on Athletic Performance, Muscle Strength, and Hypertrophy in Male Volleyball Players","8wBFR_rope","Inclusion Criteria:\n\n* Being healthy\n* Male volleyball athletes\n* Willing to maintain the intervention for all sessions\n\nExclusion Criteria:\n\n* Being under 18 years old\n* Having a chronic disease\n* Contraindications for exercise","25 Years",{"count":262,"type":22},26,[65],"The study will be conducted during the preparatory period of the volleyball players and will span eight weeks. Throughout this period, athletes will continue their regular volleyball training four days per week, while the experimental group (n = 10) will perform rope training with blood flow restriction (BFR) twice per week, and the control group (n = 10) will perform the same rope training without BFR. Assessments will be carried out at the beginning of the 8-week period (pre-test) and at the end of the intervention (post-test). For both groups, all exercises will target the upper-extremity muscle groups. During the study, participants will be instructed to avoid consuming any medications, engaging in additional strenuous physical activities, and using any techniques or ergogenic aids that might influence the results. In both testing sessions, a standardized warm-up protocol will be implemented, consisting of a 5-minute treadmill run at 9 km\u002Fh on a Sprint Runner device (Hoggan Health Industries, Draper, UT), followed by 3 minutes of light full-body stretching. This warm-up procedure will be applied consistently across both groups to ensure standardization.",[266,31,145],"Volleyball",[268,269,270,271],"blood flow restriction","rope","volleyball","hypertrophy","2025-12-26",{"date":274,"type":45},"2026-01-08",{"date":276,"type":22},"2025-12-11",{"date":278,"type":22},"2026-03-05",{"name":280,"class":52},"Karabuk University",{"id":282,"slug":283,"hasResults":11,"nctId":284,"briefTitle":285,"officialTitle":285,"acronym":286,"eligibilityCriteria":287,"healthyVolunteers":11,"sex":99,"minAge":288,"maxAge":137,"enrollmentInfo":289,"targetDuration":4,"studyType":63,"phases":291,"briefSummary":292,"conditions":293,"keywords":296,"overallStatus":73,"whyStopped":4,"lastUpdateSubmitDate":299,"lastUpdatePostDateStruct":300,"startDateStruct":302,"completionDateStruct":304,"leadSponsor":306,"locationsCount":4},"100613442","effects-of-pilates-training-on-ankle-proprioception-postural-control-and-performance-in-footballers-with-chronic-ankle-instability-100613442","NCT07266649","Effects of Pilates Training on Ankle Proprioception, Postural Control and Performance in Footballers With Chronic Ankle Instability","CAI","Inclusion Criteria:\n\nMale footballers aged 22-35\n\n* History of unilateral ankle sprain in past 12 months\n* Inability to bear weight post-injury\n* CAIT score \\\u003C 24\n* Minimum of 1-year experience in football\n\nExclusion Criteria:\n\n* Bilateral ankle sprains\n* Lower limb fractures or surgeries\n* Neurological conditions (e.g., MS, CMT, Stroke)","22 Years",{"count":290,"type":22},88,[65],"This study aims to contribute to the effects of Pilates training on ankle proprioception, postural control, and performance in football players with chronic ankle instability. Eighty eight participants will be randomly allocated into two groups and will receive both Pilates and balance training for eight weeks. it is hypothesized that the group that will receive Pilates taring will produce greater improvements as compared to other group.",[294,31,295],"Proprioception, Postural Balance","Chronic Ankle Instability, CAI",[297,150,298,31],"Chronic Ankle Instability","Postural Control","2025-11-24",{"date":301,"type":45},"2025-12-05",{"date":303,"type":22},"2025-11-25",{"date":305,"type":22},"2026-05-30",{"name":307,"class":52},"Lahore University of Biological and Applied Sciences",{"id":309,"slug":310,"hasResults":11,"nctId":311,"briefTitle":312,"officialTitle":313,"acronym":4,"eligibilityCriteria":314,"healthyVolunteers":11,"sex":18,"minAge":315,"maxAge":19,"enrollmentInfo":316,"targetDuration":4,"studyType":63,"phases":318,"briefSummary":319,"conditions":320,"keywords":4,"overallStatus":41,"whyStopped":4,"lastUpdateSubmitDate":325,"lastUpdatePostDateStruct":326,"startDateStruct":328,"completionDateStruct":330,"leadSponsor":332,"locationsCount":53},"100611439","acute-effects-of-different-warm-up-protocols-in-competitive-young-swimmers-100611439","NCT07240597","Acute Effects of Different Warm-Up Protocols in Competitive Young Swimmers","Acute Effects of Different Potentiation Protocols During Warm-Up in Competitive Young Swimmers: A Randomized Crossover Trial","Inclusion Criteria:\n\n* Active participation in competitive training programs (at least 10 hours per week), at least one year of experience in competitions organized by the Italian Swimming Federation, and no recent injuries.\n* Experience of resistance training for at least 6 months\n\nExclusion Criteria:\n\n* Irregular training participation\n* History of injuries in the 6 months prior to the study","11 Years",{"count":317,"type":22},15,[65],"Several warm-up strategies are commonly employed by athletes to optimize athletic performance and minimize the risk of injury. Recently, Post-Activation Performance Enhancement (PAPE) has been demonstrated to be effective in improving athletic performance. Nevertheless, the difference with the general warm-up is still unclear and poorly studied. Conventionally, short-term performance improvements achieved after brief periods of maximal activity have been attributed to PAP, a muscle memory mechanism that generates involuntary and short-lived effects (\\~28 seconds). This condition appears to be activated only by a history of localized maximal contractions. In the literature, various conditioning protocols with differing durations and intensities have been explored, often finding conflicting results in terms of athletic performance. In swimming, few PAPE warm-up protocols outside the pool have been studied, despite their potential usefulness considering the waiting times before competitions.\n\nTherefore, this study explores the effects of three different warm-up protocols in young swimmers. Specifically, different exercise protocols will be included in the athletes' usual warm-up routine, aimed at improving athletic performance through PAPE effects. In line with existing literature, the performance parameters examined are the countermovement jump (CMJ) and the times recorded for covering race distances ( 25 m, 50 m, 100 m). In addition, skin temperature, heart rate (HR), muscle oxygen saturation (SmO2), and perceived exertion (RPE) are also measured after the protocols to investigate possible relationships with performance measures. Nevertheless, the primary aim of this study is to compare different warm-up protocols in young swimmers to maximize their athletic performance.",[321,322,323,31,324],"Athletes","Post Activation Potentiation","Countermovement Jump","Warm-up","2025-11-16",{"date":327,"type":45},"2025-11-21",{"date":329,"type":22},"2025-12-02",{"date":331,"type":22},"2026-02",{"name":333,"class":52},"University of Palermo",{"id":335,"slug":336,"hasResults":11,"nctId":337,"briefTitle":338,"officialTitle":339,"acronym":340,"eligibilityCriteria":341,"healthyVolunteers":17,"sex":99,"minAge":19,"maxAge":137,"enrollmentInfo":342,"targetDuration":4,"studyType":63,"phases":343,"briefSummary":344,"conditions":345,"keywords":346,"overallStatus":73,"whyStopped":4,"lastUpdateSubmitDate":352,"lastUpdatePostDateStruct":353,"startDateStruct":355,"completionDateStruct":357,"leadSponsor":359,"locationsCount":53},"100601114","chronic-grape-extract-in-crosstraining-athletes-a-randomized-crossover-trial-100601114","NCT07106281","Chronic Grape Extract in Crosstraining Athletes: A Randomized Crossover Trial","Effect of Chronic Grape Extract Supplementation in Trained Cross-training Athletes: A Randomized, Triple-blinded, Placebo-Controlled Crossover Study","CROSSUVA","Inclusion Criteria:\n\n* Age: 18-35 years.\n* Body mass index: 18.5-30 kg\u002Fm2.\n* Ability to understand the instructions, objectives, and study protocol.\n* Minimum of 3 years of experience in crosstraining, with at least 6 hours of weekly training over the past 3 months.\n* Resident on the island of Tenerife.\n\nExclusion Criteria:\n\n* History of a significant adverse cardiovascular event, renal insufficiency, cirrhosis, eating disorder, weight control surgical intervention, or type 2 diabetes mellitus.\n* Any chronic pathology in which the intake of nutritional supplements, especially use of antioxidant supplements during the 4 weeks prior to the start of the study.\n* Any condition that, in the investigator's judgment, would impair the ability to participate in the study or represent a personal risk to the participant.\n* Use of medications that may affect the study results.\n* Unstable body weight for 3 months prior to the start of the study (\\> 4 kg loss or gain in weight).\n* Active tobacco abuse or illicit drug use, or history of treatment for alcohol abuse.\n* On a special diet or prescribed for other reasons (e.g., celiac disease).",{"count":200,"type":22},[65],"The aim of this study is to investigate the effect of cronic GSE intake in crosstraining may have a favorable impact on biochemical markers, recovery, and performance.",[31],[347,348,349,350,351],"grape seed extract","muscle damage","concurrent exercise","nutrition","recovery","2025-07-29",{"date":354,"type":45},"2025-08-06",{"date":356,"type":22},"2025-09-01",{"date":358,"type":22},"2026-01-31",{"name":360,"class":52},"Universidad de Granada",{"id":362,"slug":363,"hasResults":11,"nctId":364,"briefTitle":365,"officialTitle":366,"acronym":367,"eligibilityCriteria":368,"healthyVolunteers":17,"sex":226,"minAge":4,"maxAge":4,"enrollmentInfo":369,"targetDuration":371,"studyType":24,"phases":4,"briefSummary":372,"conditions":373,"keywords":377,"overallStatus":41,"whyStopped":4,"lastUpdateSubmitDate":383,"lastUpdatePostDateStruct":384,"startDateStruct":386,"completionDateStruct":387,"leadSponsor":389,"locationsCount":53},"100577875","impact-of-delivery-method-elite-athletes-100577875","NCT06803979","Impact of Delivery Method Elite Athletes.","The Impact of Delivery Method on the Performance of Elite Athletes.","IDEA","Inclusion Criteria:\n\n\\- Elite female athletes meeting representation limits and included in national teams organized under the Czech Olympic Committee and individual sports federations.\n\nExclusion Criteria:\n\n\\- Any male",{"count":370,"type":22},500,"100 Years","Labor itself can occur spontaneously vaginally, with the help of extraction methods, or via cesarean section. It can also be planned or awaited for the spontaneous onset of uterine contractions. Each method has its advantages and disadvantages regarding potential damage to the pelvic floor and its stability in vaginal delivery or extraction methods, or concerning the stability of the abdominal wall with subsequent wound healing after a cesarean section.\n\nThe aim of the study is to retrospectively and prospectively determine the impact of the method of delivery on the performance of female athletes through a questionnaire study. Investigators would like to answer the question of whether cesarean delivery means a later return to training for athletes, whether pregnancy is problematic for female athletes in relation to their BMI, and whether pregnancy often signifies the end of a sports career for female athletes. The questionnaire also includes questions regarding overall women's health-menstrual cycle, incontinence, and mental health of female athletes. Prospectively, the questionnaire will be sent to all female athletes who meet representation limits once a year and for two years after retiring from the national team.",[374,31,375,376,321],"Delivery","Caesarean Section","Pregnancy",[378,153,379,380,381,382],"delivery","caesarean section","pregnancy","athletes","women health","2025-03-16",{"date":385,"type":45},"2025-03-18",{"date":383,"type":22},{"date":388,"type":22},"2040-01-01",{"name":390,"class":391},"Faculty Hospital Kralovske Vinohrady","OTHER_GOV",{"id":393,"slug":394,"hasResults":11,"nctId":395,"briefTitle":396,"officialTitle":397,"acronym":4,"eligibilityCriteria":398,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":399,"enrollmentInfo":400,"targetDuration":4,"studyType":63,"phases":402,"briefSummary":403,"conditions":404,"keywords":4,"overallStatus":41,"whyStopped":4,"lastUpdateSubmitDate":409,"lastUpdatePostDateStruct":410,"startDateStruct":412,"completionDateStruct":414,"leadSponsor":416,"locationsCount":53},"100463037","acoustic-stimulation-during-restricted-sleep-after-sleep-deprivation-100463037","NCT05309473","Acoustic Stimulation During Restricted Sleep After Sleep Deprivation","Slow-wave Sleep Enhancement Using Acoustic Stimulation to Facilitate Performance Recovery During Restricted Sleep After Sleep Deprivation","Inclusion Criteria:\n\n* Healthy men and non-pregnant, non-lactating women 18 to 39 years of age (inclusive)\n* Must demonstrate adequate comprehension of the protocol, by achieving a score of at least 80% correct on a short multiple-choice quiz. Individuals who fail to achieve a passing score on the initial quiz will be given one opportunity to retest after a review of protocol information. Individuals who fail the comprehension assessment for the second time will be disqualified.\n\nExclusion Criteria:\n\n* You must have learned English as your first language\n* You must have a body mass index (BMI) below 30 (this is a mathematical calculation of your height and weight)\n* You must not have current or a history of sleeping problems (for example, insomnia or sleep apnea), or symptoms that indicate a potential sleep disorder\n* You must get an average of 6-9 hours of sleep per night and maintain a normal sleep\u002Fwake schedule\n* You must not drink excessive amounts of caffeine, alcohol, or smoke cigarettes regularly\n* You must not be on certain medications (determined on a case by case basis)\n* You must test negative for illicit drugs\n* Women must not be pregnant or nursing\n* You must not be participating in another ongoing clinical trial\n* You must have a social security number or tax identification number in order to be paid for screening and participation in the study\n* You cannot have a history of the following conditions: Cardiovascular disease, a neurologic disorder, pulmonary disease requiring inhaler use, kidney disease or kidney abnormalities, liver disease of liver abnormalities, a history of psychiatric disorder requiring hospitalization or medication within the last two years or for a continuous period of more than 6 months in the last ten years","39 Years",{"count":401,"type":22},44,[65],"The purpose of this study is to determine if brief sounds or tones presented within a restricted period of recovery sleep after a period of sleep deprivation will enhance restorative properties and improve performance during a subsequent period of wakefulness.",[405,406,407,31,408],"Sleep Deprivation","Sleep Restriction","Acoustic Stimulation","Alertness","2024-04-22",{"date":411,"type":45},"2024-04-23",{"date":413,"type":45},"2022-03-14",{"date":415,"type":22},"2026-10",{"name":417,"class":418},"Walter Reed Army Institute of Research (WRAIR)","FED"]