[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Beijing Sport University\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":283},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,11,0,[8,50,85,105,129,151,177,198,221,238,256],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":29,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":38,"lastUpdatePostDateStruct":39,"startDateStruct":42,"completionDateStruct":44,"leadSponsor":46,"locationsCount":49},"100639890","elastic-band-resistance-and-breathing-training-for-older-adults-with-pulmonary-function-impairment-100639890",false,"NCT07612072","Elastic-Band Resistance and Breathing Training for Older Adults With Pulmonary Function Impairment","Effects of Elastic-Band Resistance Training With or Without Breathing Exercise on Pulmonary Function and Functional Performance in Community-Dwelling Older Adults With Pulmonary Function Impairment: A Randomized Controlled Trial","EBBT-PFI","Inclusion Criteria:\n\n* Age 60 to 85 years\n* Pulmonary function impairment identified by community-based spirometry screening\n* Community-dwelling older adults\n* Able to communicate and walk independently\n* Willing to participate in the 12-week intervention and all study assessments\n* Provided written informed consent\n\nExclusion Criteria:\n\n* Acute or unstable cardiovascular, respiratory, or severe musculoskeletal disease that made exercise training unsafe\n* Recent acute exacerbation, surgery, severe infection, or other health event that could affect safe participation\n* Significant cognitive impairment, communication disorder, or inability to cooperate with training or assessments\n* Currently receiving systematic pulmonary rehabilitation or regular structured exercise training that could affect the intervention effect\n* Unable to meet spirometry quality-control requirements\n* Unable to complete key baseline outcome assessments","ALL","60 Years","85 Years",{"count":21,"type":22},75,"ESTIMATED","INTERVENTIONAL",[25],"NA","The goal of this clinical trial is to learn whether elastic-band resistance training, with or without breathing training, can improve lung function and physical function in older adults with pulmonary function impairment living in the community. It will also learn about the safety and feasibility of these exercise programs.\n\nThe main questions it aims to answer are:\n\nDoes elastic-band resistance training improve lung function, lower-limb muscle strength, walking ability, and exercise tolerance?\n\nDoes adding structured breathing training to elastic-band resistance training provide additional benefits for lung function and respiratory-related health status?\n\nAre these exercise programs safe and acceptable for older adults in a community setting?\n\nResearchers will compare three groups: elastic-band resistance training plus breathing training, elastic-band resistance training alone, and usual health education. This will help determine whether elastic-band resistance training is helpful and whether breathing training adds extra benefit.\n\nParticipants will:\n\nTake part in a 12-week study\n\nBe assigned by chance to one of three groups\n\nAttend supervised exercise sessions 3 times per week if assigned to an exercise group\n\nReceive usual health education and daily activity guidance\n\nComplete lung function tests, muscle strength tests, physical function tests, and questionnaires at the start of the study, at 6 weeks, and at 12 weeks",[28],"Respiration Disorders",[30,31,32,33,34,35,36],"Pulmonary Function Impairment","Elastic-Band Resistance Training","Older Adults","Pulmonary Function","Breathing Training","Exercise Intervention","Respiratory Health","NOT_YET_RECRUITING","2026-06-30",{"date":40,"type":41},"2026-07-02","ACTUAL",{"date":43,"type":22},"2026-06-10",{"date":45,"type":22},"2026-09-16",{"name":47,"class":48},"Beijing Sport University","OTHER",1,{"id":51,"slug":52,"hasResults":11,"nctId":53,"briefTitle":54,"officialTitle":55,"acronym":4,"eligibilityCriteria":56,"healthyVolunteers":57,"sex":58,"minAge":59,"maxAge":60,"enrollmentInfo":61,"targetDuration":4,"studyType":23,"phases":63,"briefSummary":64,"conditions":65,"keywords":70,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":38,"lastUpdatePostDateStruct":79,"startDateStruct":80,"completionDateStruct":82,"leadSponsor":84,"locationsCount":49},"100634963","effects-of-cistanche-supplementation-on-anaerobic-exercise-performance-and-recovery-in-men-with-different-athletic-training-levels-100634963","NCT07546513","Effects of Cistanche Supplementation on Anaerobic Exercise Performance and Recovery in Men With Different Athletic Training Levels","Effects of Cistanche Supplementation on Anaerobic Exercise Performance and Recovery in Men With Different Athletic Training Levels: A Double-Blind, Randomized, Placebo-Controlled Trial","Inclusion Criteria:\n\n* Male, aged 18 to 25 years\n* Body mass index (BMI) between 18.5 and 25.0 kg\u002Fm²\n* Able and willing to provide written informed consent\n* Willing to comply with study procedures, supplementation, training, and assessments\n* Belonging to one of the following athletic training strata:\n* High-level elite stratum: Chinese National Level-1 Athlete standard in sprint-related events, regular training in past 12 months and active during study\n* Amateur stratum: regular exercise-training background in past 12 months without National Level-1 status\n\nExclusion Criteria:\n\n* Use of steroids or ergogenic supplements during study\n* Known cardiovascular, metabolic, musculoskeletal, or other conditions making participation unsafe or affecting outcomes\n* Current use of medications affecting muscle growth, recovery, hormones, or high-intensity performance\n* Current injury or limitation preventing safe participation\n* Known allergy or intolerance to supplement\u002Fplacebo ingredients\n* Participation in another clinical trial or structured intervention during study period\n* Inability or unwillingness to comply with protocol\n* Any other condition deemed unsuitable by investigators",true,"MALE","18 Years","25 Years",{"count":62,"type":22},56,[25],"This study is a double-blind, randomized, placebo-controlled trial designed to examine whether 8 weeks of Cistanche deserticola supplementation, when combined with a standardized anaerobic training program, can improve anaerobic exercise performance, recovery, and selected body composition outcomes in young adult men with different athletic training levels.\n\nParticipants will be assigned to receive either Cistanche deserticola extract or a matched placebo while completing the same supervised anaerobic training program. The study will assess changes in anaerobic performance, including Wingate test outcomes and jump performance, as well as recovery-related indicators such as blood lactate, creatine kinase, malondialdehyde, testosterone, cortisol, and the testosterone-to-cortisol ratio. Body composition outcomes, including body fat percentage and skeletal muscle mass, will also be evaluated.\n\nThe purpose of this study is to determine whether Cistanche deserticola supplementation provides additional benefits beyond training alone, and whether these effects differ between highly trained and recreationally trained participants.",[66,67,68,69],"Athlete","Elite Athlete","Sport Performance","Exercise Recovery",[71,72,73,74,75,76,77,78],"Cistanche","anaerobic performance","exercise recovery","explosive power","lactate","muscle damage","body composition","randomized controlled trial",{"date":40,"type":41},{"date":81,"type":22},"2026-06-25",{"date":83,"type":22},"2026-09-15",{"name":47,"class":48},{"id":86,"slug":87,"hasResults":11,"nctId":88,"briefTitle":89,"officialTitle":89,"acronym":4,"eligibilityCriteria":90,"healthyVolunteers":57,"sex":17,"minAge":18,"maxAge":91,"enrollmentInfo":92,"targetDuration":4,"studyType":23,"phases":94,"briefSummary":95,"conditions":96,"keywords":4,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":98,"lastUpdatePostDateStruct":99,"startDateStruct":101,"completionDateStruct":103,"leadSponsor":104,"locationsCount":4},"100640864","the-effects-of-immersive-virtual-reality-based-exergaming-combined-with-transcranial-direct-current-stimulation-on-executive-functions-in-healthy-older-adults-100640864","NCT07591194","The Effects of Immersive Virtual Reality-Based Exergaming Combined With Transcranial Direct Current Stimulation on Executive Functions in Healthy Older Adults","Inclusion Criteria:\n\n(1) Age between 60 to 70 years old; (2) Right-handed (Edinburgh Handedness Inventory (Chinese version) \\> 40); (3) Normal overall cognitive function (Montreal Cognitive Assessment (Beijing version) ≥ 26).\n\nExclusion Criteria:\n\n(1) Musculoskeletal injury; (2) neurological\u002Fneurodegenerative disorders (e.g., Alzheimer's disease); (3) history of brain infections or cerebrovascular diseases; (4) psychiatric disorders (e.g., major depressive disorder, schizophrenia); (5) unstable or chronic medical conditions (e.g., cardiac disease, seizures (personal\u002Ffamily history)); (6) hearing and visual impairments (e.g., color blindness and conditions severely affecting the ability to see the screen or distinguish colors); (7) metal implants (e.g., pacemakers); (8) brain stimulation or exercise training intervention within the past 6 months; (9) failure to meet safety criteria for brain stimulation (e.g., pregnancy)","70 Years",{"count":93,"type":22},24,[25],"The goal of this clinical trial is to investigate the acute effects of immersive virtual reality (VR)-based exergaming combined with transcranial direct current stimulation (tDCS) on executive functions in healthy older adults. The main questions it aims to answer are:\n\n* Does VR-based exergaming combined with tDCS improve executive function performance in healthy older adults compared with a control condition?\n* Do single interventions (tDCS alone or VR-based exergaming alone) improve executive function performance compared with the control condition?\n* Does the combined intervention produce greater improvements in executive function performance than either intervention alone? Researchers will compare four intervention conditions to evaluate differences in executive function performance following each session.\n\nParticipants will:\n\n* Complete four intervention sessions in a randomized crossover sequence, with a washout period of at least 7 days between sessions\n* Receive the following intervention conditions:\n* sham-tDCS + VR-video\n* tDCS + VR-video\n* sham-tDCS + VR-exergaming\n* tDCS + VR-exergaming\n* Complete executive function assessments immediately after each session, including:\n* the Flanker task for inhibitory control\n* the more-odd shifting task for cognitive flexibility\n* the Corsi block-tapping task for working memory",[97],"Healthy Older Adults","2026-05-09",{"date":100,"type":41},"2026-05-15",{"date":102,"type":22},"2026-05-20",{"date":81,"type":22},{"name":47,"class":48},{"id":106,"slug":107,"hasResults":11,"nctId":108,"briefTitle":109,"officialTitle":110,"acronym":4,"eligibilityCriteria":111,"healthyVolunteers":11,"sex":17,"minAge":59,"maxAge":112,"enrollmentInfo":113,"targetDuration":4,"studyType":23,"phases":115,"briefSummary":116,"conditions":117,"keywords":119,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":122,"lastUpdatePostDateStruct":123,"startDateStruct":125,"completionDateStruct":126,"leadSponsor":128,"locationsCount":4},"100635830","telerehabilitation-for-patellofemoral-pain-100635830","NCT07557784","Telerehabilitation for Patellofemoral Pain","Telerehabilitation Versus Face-to-Face Supervised Rehabilitation for Patellofemoral Pain: A Randomized Non-Inferiority Trial","* Inclusion Criteria\n\n  * Aged 18 to 45 years\n  * Clinical diagnosis of patellofemoral pain\n  * History of anterior or retropatellar knee pain for at least 3 months\n  * Pain provoked by at least two of the following activities: stair ambulation, squatting, running, jumping, or prolonged sitting\n  * Baseline knee pain intensity of at least 3\u002F10 on the Numerical Rating Pain Scale\n  * Willing and able to participate in the rehabilitation program and follow-up assessments\n  * Able to provide written informed consent\n* Exclusion Criteria\n\n  * Previous knee surgery\n  * History of patellar dislocation or instability\n  * Evidence of ligament injury, meniscal injury requiring separate management, moderate to severe knee osteoarthritis, or other major structural knee pathology\n  * Concurrent hip, ankle, lumbar spine, or other musculoskeletal disorders substantially affecting lower limb function\n  * Neurological disorders affecting movement or balance\n  * Severe cardiopulmonary or systemic disease contraindicating exercise\n  * Received structured lower limb rehabilitation within the previous 3 months\n  * Pregnancy\n  * Any other condition judged by the investigators to make participation unsuitable","45 Years",{"count":114,"type":22},106,[25],"Patellofemoral pain (PFP) is a common musculoskeletal condition characterized by pain around or behind the patella during activities such as stair ambulation, squatting, running, jumping, and prolonged sitting. Exercise therapy combined with patient education is considered first-line treatment, and supervised rehabilitation is commonly used to improve adherence and clinical outcomes.\n\nTelerehabilitation may increase accessibility and reduce time and travel burden, but high-quality evidence remains limited regarding whether telerehabilitation provides outcomes that are not inferior to conventional face-to-face supervised rehabilitation in individuals with PFP.\n\nThis study is a randomized, assessor-blinded, non-inferiority trial designed to compare telerehabilitation with face-to-face supervised rehabilitation in individuals with patellofemoral pain. The trial will evaluate whether telerehabilitation is not inferior to face-to-face supervised rehabilitation in improving pain and knee-related function, while also examining psychological outcomes, self-satisfaction, and adherence.",[118],"Patellofemoral Pain, PFP",[120,121],"Telerehabilitation","Patellofemoral Pain","2026-04-25",{"date":124,"type":41},"2026-04-29",{"date":102,"type":22},{"date":127,"type":22},"2027-03-20",{"name":47,"class":48},{"id":130,"slug":131,"hasResults":11,"nctId":132,"briefTitle":133,"officialTitle":134,"acronym":4,"eligibilityCriteria":135,"healthyVolunteers":11,"sex":136,"minAge":59,"maxAge":112,"enrollmentInfo":137,"targetDuration":4,"studyType":23,"phases":139,"briefSummary":140,"conditions":141,"keywords":142,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":122,"lastUpdatePostDateStruct":146,"startDateStruct":147,"completionDateStruct":148,"leadSponsor":150,"locationsCount":49},"100635831","gait-retraining-for-runners-with-patellofemoral-pain-100635831","NCT07557797","Gait Retraining for Runners With Patellofemoral Pain","Gait Retraining Intervention for Female Runners With Patellofemoral Pain: Randomized Controlled Trial","Inclusion Criteria:\n\n* Female, Age 18-45 years\n* Unilateral\u002Fbilateral anterior knee pain \\> 4 weeks\n* VAS pain ≥ 3\u002F10 during running and ≥ 2 of the following: jumping, squatting, kneeling, stairs, prolonged sitting, or resisted knee extension\n* Running ≥ 15 km per week\n* Natural rearfoot striker\n\nExclusion Criteria:\n\n* Acute trauma, history of patellar dislocation, meniscal\u002Fchondral lesions\n* Prior knee surgery or injection in past 12 months\n* Rheumatologic, neurologic, or degenerative disease\n* Pregnancy","FEMALE",{"count":138,"type":22},44,[25],"Patellofemoral pain (PFP) is a common overuse injury in runners. Increased patellofemoral joint stress (PFJS) is an important biomechanical factor associated with PFP. Gait retraining, especially cadence modification, may reduce PFJS and improve symptoms, but evidence from randomized controlled trials remains limited. This study investigated whether wearable device-assisted gait retraining was more effective than education alone in reducing pain, improving function, and altering running biomechanics in female runners with PFP.",[118],[143,144,145],"Patellofemoral pain","gait retraining","runner",{"date":124,"type":41},{"date":100,"type":22},{"date":149,"type":22},"2026-12-15",{"name":47,"class":48},{"id":152,"slug":153,"hasResults":11,"nctId":154,"briefTitle":155,"officialTitle":155,"acronym":156,"eligibilityCriteria":157,"healthyVolunteers":57,"sex":17,"minAge":59,"maxAge":158,"enrollmentInfo":159,"targetDuration":4,"studyType":161,"phases":4,"briefSummary":162,"conditions":163,"keywords":167,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":169,"lastUpdatePostDateStruct":170,"startDateStruct":172,"completionDateStruct":174,"leadSponsor":176,"locationsCount":4},"100620684","investigation-of-autonomic-stress-response-patterns-in-college-students-with-varying-physical-activity-levels-100620684","NCT07360821","Investigation of Autonomic Stress Response Patterns in College Students With Varying Physical Activity Levels","ANS Stress\u002FPA","Inclusion Criteria:\n\nHealthy young adults aged 18-25 years\n\nBody Mass Index (BMI) within the range of 18.5-23.9 kg\u002Fm 2\n\nNo history of systematic professional athletic training (for sedentary group) or confirmed training background (for athlete groups)\n\nNo exercise contraindications or history of cardiovascular, respiratory, or metabolic diseases\n\nNo family history of sudden cardiac death\n\nAbility to understand the study protocol and sign the informed consent form\n\nExclusion Criteria:\n\nHistory of limb sports injury within the past 6 months or unhealed fractures\n\nHabits of smoking or chronic alcohol consumption\n\nPresence of implanted electronic devices (e.g., pacemakers)\n\nClinical diagnosis of psychiatric disorders such as anxiety or depression\n\nRecent use of medications affecting autonomic or cardiovascular function\n\nRegular practice of meditation or ongoing psychotherapy\n\nIrregular menstrual cycles (for female participants)\n\nPeripheral neuropathy or other autonomic nervous system disorders","30 Years",{"count":160,"type":22},60,"OBSERVATIONAL","This study aims to investigate the differences in cardiovascular stress response patterns among individuals with various physical activity levels (sedentary controls and different types of athletes). By synchronously monitoring ECG, heart rate, skin sympathetic nerve activity (SKNA), blood pressure, and cardiac output, the study will characterize physiological dynamics during resting, orthostatic challenge, cold pressor stress, and maximal exercise.",[164,165,166],"Autonomic Nervous System Activity","Cardiovascular","Physical Activity Level",[168],"SKNA; HRV; Blood Pressure Variability; Athletes; Cardiopulmonary Exercise Testing","2026-01-17",{"date":171,"type":41},"2026-01-22",{"date":173,"type":22},"2026-02-25",{"date":175,"type":22},"2026-07-30",{"name":47,"class":48},{"id":178,"slug":179,"hasResults":11,"nctId":180,"briefTitle":181,"officialTitle":182,"acronym":4,"eligibilityCriteria":183,"healthyVolunteers":11,"sex":17,"minAge":184,"maxAge":185,"enrollmentInfo":186,"targetDuration":4,"studyType":161,"phases":4,"briefSummary":187,"conditions":188,"keywords":4,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":190,"lastUpdatePostDateStruct":191,"startDateStruct":193,"completionDateStruct":195,"leadSponsor":197,"locationsCount":4},"100613309","tai-chi-improves-sleep-quality-in-mild-to-moderate-chronic-insomnia-patients-100613309","NCT07264907","Tai Chi Improves Sleep Quality in Mild to Moderate Chronic Insomnia Patients","Tai Chi Improves Sleep Quality in Patients With Mild to Moderate Chronic Insomnia","Inclusion Criteria:\n\n1. Age 40 to 69, gender unlimited;\n2. Insomnia symptoms (difficulty falling asleep, frequent awakenings during sleep, early morning awakening, etc.) occurring three or more times per week for three months or longer (meeting DSM-5 diagnostic criteria for chronic insomnia and International Classification of Sleep Disorders standards); 3.7 points \\\u003CISI baseline score ≤ 21 points (mild to moderate insomnia);\n\n4\\. The patient is dissatisfied (option 3) or very dissatisfied (option 4) with their current sleep 5. The incubation period or wake time after falling asleep is more than 30 minutes, and the total sleep time is less than 6.5 hours per day; 6. Willing to follow the exercise prescription and coach's guidance, and cooperate with the exercise intervention for 6 weeks; 7. Being able to maintain consistent lifestyle and sleep patterns throughout the study; 8. Fixed residence and no expectation of moving or traveling within 6 weeks; 9. Sign the informed consent form.\n\nExclusion Criteria:\n\n1. Exclude diseases that affect sleep (such as tumors, dementia, obstructive sleep apnea, etc.);\n2. Taking medications that may affect sleep (such as steroid hormones, sleeping pills, psychotropic drugs);\n3. Abuse of alcohol or drugs in the last 3 months;\n4. Liver or kidney dysfunction;\n5. History of severe cardiovascular and cerebrovascular diseases;\n6. History of mental illness;\n7. Expect to work night shifts or travel across time zones or sleep irregularly during the study period;\n8. Participated in other intervention clinical trials, including drugs, nutritional preparations and medical devices, within 3 months before the study.","40 Years","69 Years",{"count":160,"type":22},"What are the requirements for participating in this study?\n\n1. Age 40 to 69, gender unlimited;\n2. Insomnia symptoms (difficulty falling asleep, frequent awakenings during sleep, early morning awakening, etc.) occurring three or more times per week for three months or longer (meeting DSM-5 diagnostic criteria for chronic insomnia and International Classification of Sleep Disorders standards); 3.7 points \\\u003CISI baseline score ≤ 21 points (mild to moderate insomnia);\n\n4\\. The patient is dissatisfied (option 3) or very dissatisfied (option 4) with their current sleep 5. The incubation period or wake time after falling asleep is more than 30 minutes, and the total sleep time is less than 6.5 hours per day; 6. Willing to follow the exercise prescription and coach's guidance, and cooperate with the exercise intervention for 6 weeks; 7. Being able to maintain consistent lifestyle and sleep patterns throughout the study; 8. Fixed residence and no expectation of moving or traveling within 6 weeks; 9. Sign the informed consent form.\n\nYou are not eligible to participate in this study if you meet any of the following criteria:\n\n1. Exclude diseases that affect sleep (such as tumors, dementia, obstructive sleep apnea, etc.);\n2. Taking medications that may affect sleep (such as steroid hormones, sleeping pills, psychotropic drugs);\n3. Abuse of alcohol or drugs in the last 3 months;\n4. Liver or kidney dysfunction;\n5. History of severe cardiovascular and cerebrovascular diseases;\n6. History of mental illness;\n7. Expect to work night shifts or travel across time zones or sleep irregularly during the study period;\n8. Participated in other intervention clinical trials, including drugs, nutritional preparations and medical devices, within 3 months before the study.\n\nWhat will I experience if I participate in this study? If eligible, participants will be randomly assigned by physicians to one of two study phases: the screening and baseline assessment phase, or the intervention and follow-up phase. The trial consists of three phases, each containing two phases (experimental or control, lasting 1-2 weeks). After enrollment, participants will be randomly assigned to either the Tai Chi intervention group or the walking control group. Throughout the study, participants must cooperate with physicians to complete relevant questionnaires and attend scheduled follow-up visits.\n\nWhat might be the benefits of participating in this study? The research team will cover all expenses for the exercise program. Participants will receive free exercise training, physiological counseling, and standardized assessments throughout the study, including follow-up sessions. Our previous sports medicine research shows that 12 weeks of Tai Chi therapy can significantly improve insomnia symptoms.\n\nWhat are the risks of participating in this study? Participants who have not exercised for a long time may have adverse reactions such as muscle pain and joint pain caused by exercise in the early stage of the experiment or during the study, or even lead to the termination of the experiment.\n\nIs participation in this study mandatory? No, participation in this study is entirely voluntary.\n\nCan I quit the study midway? Yes, you can opt out at any time, and this will not affect your legal right to continue regular checkups or treatments.\n\nAre my personal information confidential? Your personal privacy will be strictly protected within the bounds of applicable laws. Monitoring officers, auditors, ethics committees, and management authorities shall be permitted to directly access participants 'original medical records to verify clinical trial procedures and data, provided such access does not violate applicable laws and regulations or infringe upon participants' privacy. Throughout the study, participants have the right to withdraw from the research at any time without facing discrimination, retaliation, or disruption of medical services. All personal information collected during the study remains confidential. Participants are entitled to consult our physicians with any questions at any time.\n\nPatient Statement (Please tick in parentheses):\n\n1. I have reviewed the relevant research materials for this study (version v1.0)···········□\n2. I have carefully considered the matter, consulted a doctor about the relevant issues, and received satisfactory answers······□\n3. I understand that participation in this study is voluntary and that I have the right to withdraw from this study at any time without any reason without affecting my medical treatment and rights·····□\n4. I understand that my relevant materials will be reviewed by the research unit or members of the strict management agency in this study. I agree to the above personnel reviewing and using my relevant materials. ·······················□\n5. I agree to participate in this study·····························□",[189],"Insomnia","2025-11-24",{"date":192,"type":41},"2025-12-04",{"date":194,"type":22},"2025-12-01",{"date":196,"type":22},"2026-06-01",{"name":47,"class":48},{"id":199,"slug":200,"hasResults":11,"nctId":201,"briefTitle":202,"officialTitle":202,"acronym":4,"eligibilityCriteria":203,"healthyVolunteers":57,"sex":17,"minAge":59,"maxAge":60,"enrollmentInfo":204,"targetDuration":4,"studyType":23,"phases":205,"briefSummary":206,"conditions":207,"keywords":209,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":213,"lastUpdatePostDateStruct":214,"startDateStruct":216,"completionDateStruct":218,"leadSponsor":220,"locationsCount":4},"100599789","effects-of-transcranial-direct-current-stimulation-after-short-term-immobilization-on-motor-learning-and-hand-function-in-healthy-young-adults-100599789","NCT07089056","Effects of Transcranial Direct Current Stimulation After Short-term Immobilization on Motor Learning and Hand Function in Healthy Young Adults","Inclusion Criteria:\n\n* (1) age between 18 and 25 years;\n* (2) normal or corrected-to-normal vision;\n* (3) right-handedness.\n\nExclusion Criteria:\n\n* (1) with history of pregnancy, cardiovascular disease, other physical impairments or illnesses;\n* (2) with personal or family history of mental illness;\n* (3) implanting any internal or external medical devices;",{"count":160,"type":22},[25],"The purpose of the study is to investigate the effects of short-term braking on the motor learning and fine motor skills of healthy adults, and to analyze whether transcranial direct current stimulation can alleviate the effects of braking on motor learning and fine motor skills.",[208],"Transcranial Direct Current Stimulation",[210,211,212],"Transcranial direct current stimulation","immobilization","motor learning","2025-07-29",{"date":215,"type":41},"2025-07-30",{"date":217,"type":22},"2025-07-21",{"date":219,"type":22},"2025-10-01",{"name":47,"class":48},{"id":222,"slug":223,"hasResults":11,"nctId":224,"briefTitle":225,"officialTitle":225,"acronym":4,"eligibilityCriteria":226,"healthyVolunteers":57,"sex":58,"minAge":4,"maxAge":4,"enrollmentInfo":227,"targetDuration":4,"studyType":23,"phases":228,"briefSummary":229,"conditions":230,"keywords":4,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":232,"lastUpdatePostDateStruct":233,"startDateStruct":234,"completionDateStruct":236,"leadSponsor":237,"locationsCount":4},"100600023","the-effects-of-transcranial-direct-current-stimulation-combined-with-resistance-training-on-motor-learning-in-healthy-young-adults-100600023","NCT07092098","The Effects of Transcranial Direct Current Stimulation Combined With Resistance Training on Motor Learning in Healthy Young Adults","Inclusion Criteria:\n\n* normal or corrected-to-normal vision\n* right-handed\n\nExclusion Criteria:\n\n* color blindness\n* color weakness\n* dyslexia\n* history of smoking\n* cardiovascular diseases\n* personal or family history of mental illness",{"count":62,"type":22},[25],"This study aimed to investigate whether six weeks of tDCS combined with lower-limb resistance training could enhance motor learning in healthy young adults and examined the persistence of any observed benefits.",[231],"Healthy Adults","2025-07-27",{"date":213,"type":41},{"date":235,"type":22},"2025-07-20",{"date":219,"type":22},{"name":47,"class":48},{"id":239,"slug":240,"hasResults":11,"nctId":241,"briefTitle":242,"officialTitle":242,"acronym":4,"eligibilityCriteria":243,"healthyVolunteers":57,"sex":17,"minAge":59,"maxAge":60,"enrollmentInfo":244,"targetDuration":4,"studyType":23,"phases":245,"briefSummary":246,"conditions":247,"keywords":249,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":235,"lastUpdatePostDateStruct":251,"startDateStruct":253,"completionDateStruct":254,"leadSponsor":255,"locationsCount":4},"100599790","intensity-dependent-effects-of-4-week-transcranial-direct-current-stimulation-on-motor-learning-in-healthy-young-adults-100599790","NCT07089069","Intensity-Dependent Effects of 4-week Transcranial Direct Current Stimulation on Motor Learning in Healthy Young Adults","Inclusion Criteria:\n\n1. age between 18 and 25 years; (2) normal or corrected-to-normal vision; (3) no history of pregnancy, cardiovascular disease, other physical impairments or illnesses, and no personal or family history of mental illness; (4) no implantation of any internal or external medical devices; and (5) right-handedness.\n\nExclusion Criteria:\n\n\\-",{"count":138,"type":22},[25],"The goal of this clinical trial is to investigate the effects of different intensities of transcranial direct current stimulationover primary motor cortex on motor learning in healthy adults. The main question it aims to answer is:\n\nWhich intensity of tDCS can best improve motor learning? Researchers will compare 1 mA, 2 mA, and 3 mA tDCS to sham tDCS to see which intensity of tDCS is most effective in improving the ability of motor learning.\n\nParticipants will be randomly divided into four groups and receive 4 different intensities of tDCS(1 mA, 2 mA, 3 mA and sham tDCS),and will be blinded to the type of tDCS they received. We hypothesized that anodal tDCS at 2 mA would produce the most substantial improvement in motor learning.",[248],"Transcranial Direct Current Stimulation (tDCS)",[208,212,250],"Healthy young adults",{"date":252,"type":41},"2025-07-28",{"date":235,"type":22},{"date":219,"type":22},{"name":47,"class":48},{"id":257,"slug":258,"hasResults":11,"nctId":259,"briefTitle":260,"officialTitle":261,"acronym":4,"eligibilityCriteria":262,"healthyVolunteers":57,"sex":17,"minAge":59,"maxAge":263,"enrollmentInfo":264,"targetDuration":4,"studyType":23,"phases":266,"briefSummary":267,"conditions":268,"keywords":271,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":275,"lastUpdatePostDateStruct":276,"startDateStruct":278,"completionDateStruct":280,"leadSponsor":282,"locationsCount":49},"100581372","effects-of-exercise-snacks-and-sprint-interval-training-in-overweight-adults-100581372","NCT06849453","Effects of Exercise Snacks and Sprint Interval Training in Overweight Adults","Effects of Exercise Snacks and Sprint Interval Training on Cardiovascular Function in Overweight Adults: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Men and women aged between 18 and 35 years;\n* Overweight but not obese (BMI ≥24 and ≤ 28 kg\u002Fm2);\n* Physically inactive (3 or less bouts of purposeful exercise per week);\n* Ability to understand the research details and voluntarily sign the informed consent form;\n* Non-smoker (for \\>5 years);\n* Body weight has been stable over the past six months, with no recent weight gain or loss behaviors;\n* Healthy (see exclusion criteria).\n\nExclusion Criteria:\n\n* Any chronic illness, cardiac, pulmonary, liver, or kidney abnormalities, uncontrolled hypertension, peripheral arterial disease, insulin- or non-insulin dependent diabetes or other metabolic disorders - all ascertained through preliminary screening;\n* Individuals with a history of bone, joint or neuromuscular problems or a current musculoskeletal injury ascertained through preliminary screening;\n* Abnormal electrocardiogram (ECG) results;\n* Currently taking medication that may affect physiological testing;\n* Contraindications to exercise.","35 Years",{"count":265,"type":22},45,[25],"Exploring the efficacy and acceptability of exercise snacks (ES) and sprint interval training (SIT) could provide time-efficient, low-barrier alternatives for individuals, especially those who, due to 'lack of time, environment, and equipment,' struggle to meet traditional physical activity recommendations. This research aims to investigate the effects of ES and SIT, of equal exercise volume, on overweight adults.",[269,270],"Cardiovascular Function","Cardiorespiratory Fitness",[272,273,274,269],"Exercise Snacks","Sprint Interval Training","Overweight Adults","2025-02-25",{"date":277,"type":41},"2025-02-27",{"date":279,"type":22},"2025-02-24",{"date":281,"type":22},"2025-10-31",{"name":47,"class":48},""]