[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Chengdu Sport University\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":217},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,8,0,[8,48,74,100,125,148,169,191],{"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":30,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":36,"lastUpdatePostDateStruct":37,"startDateStruct":40,"completionDateStruct":42,"leadSponsor":44,"locationsCount":47},"100644057","different-pressure-tissue-flossing-combined-with-exercise-for-chronic-ankle-instability-100644057",false,"NCT07667816","Different Pressure Tissue Flossing Combined With Exercise for Chronic Ankle Instability","Effects of Different Tissue Flossing Pressures Combined With Exercise Training on Ankle Function in Patients With Chronic Ankle Instability: A Three-Arm Randomized Controlled Trial","CAI-FLOSS","Inclusion Criteria:\n\n* Young adults aged 18 to 30 years.\n* History of at least one recurrent ankle sprain or repeated episodes of ankle giving way in the affected limb.\n* Subjective ankle instability, with or without pain, swelling, or activity limitation.\n* Reduced balance ability, movement ability, or foot and ankle function on screening assessment.\n* Symptoms lasting at least 6 months.\n* No recent structured ankle rehabilitation before enrollment.\n* No plan for vigorous additional exercise during the intervention period.\n* Willing to participate and able to provide informed consent.\n\nExclusion Criteria:\n\n* Latex allergy or intolerance to floss band material.\n* Previous ankle dislocation, fracture, complete ligament rupture, or other severe structural injury.\n* Most recent ankle sprain within 1 month before enrollment.\n* Recent ankle surgery or acute ankle injury.\n* Receipt of other ankle-related treatment, rehabilitation, or additional training during the study period.\n* Diabetes, hyperlipidemia, or other conditions that may affect vascular status.\n* Neurological disease, major musculoskeletal disease, vestibular disorder, visual disorder, or other lower-limb conditions that could affect assessment.\n* Determined by the study physician or investigator to be unsuitable for participation.","ALL","18 Years","30 Years",{"count":21,"type":22},48,"ESTIMATED","INTERVENTIONAL",[25],"NA","This study will evaluate whether tissue flossing with different pressure levels, when combined with exercise training, improves ankle function in young adults with chronic ankle instability. Forty-eight participants will be randomly assigned to one of three groups: a control exercise group, a 150 mmHg tissue flossing plus exercise group, or a 200 mmHg tissue flossing plus exercise group. All groups will complete the same 6-week rehabilitation program, three times per week. Outcomes will be assessed at baseline and after the intervention, and long-term follow-up data will also be collected.",[28,29],"Chronic Ankle Instability","Ankle Instability",[31,32,28,33,34],"Tissue Flossing","Floss Band","Ankle Rehabilitation","Exercise Therapy","NOT_YET_RECRUITING","2026-06-21",{"date":38,"type":39},"2026-06-25","ACTUAL",{"date":41,"type":22},"2026-07",{"date":43,"type":22},"2027-05",{"name":45,"class":46},"Chengdu Sport University","OTHER",1,{"id":49,"slug":50,"hasResults":11,"nctId":51,"briefTitle":52,"officialTitle":53,"acronym":4,"eligibilityCriteria":54,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":55,"enrollmentInfo":56,"targetDuration":4,"studyType":23,"phases":58,"briefSummary":59,"conditions":60,"keywords":62,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":66,"lastUpdatePostDateStruct":67,"startDateStruct":69,"completionDateStruct":71,"leadSponsor":73,"locationsCount":4},"100634842","digital-health-for-patellofemoral-pain-100634842","NCT07544940","Digital Health for Patellofemoral Pain","Digital Health-Based Rehabilitation for Participants With Patellofemoral Pain","Inclusion Criteria:\n\n* Age 18-45 years\n* Clinical diagnosis of patellofemoral pain\n* Symptoms for at least 3 months\n* Anterior or retropatellar knee pain provoked by at least two aggravating activities such as stair ambulation, squatting, running, jumping, or prolonged sitting\n* Baseline pain intensity of at least 3\u002F10 on the Numeric Rating Pain Scale\n* Ability to provide written informed consent and comply with study procedures\n\nExclusion Criteria:\n\n* Previous knee surgery\n* Patellar dislocation or obvious instability\n* Ligament injury, clinically important meniscal injury, moderate to severe knee osteoarthritis, or other major structural knee pathology\n* Major hip, ankle, or lumbar disorders substantially affecting lower-limb function\n* Neurological disorders affecting movement or balance\n* Pregnancy\n* Structured PFP rehabilitation within the previous 3 months\n* Any other condition deemed unsuitable by the investigators","45 Years",{"count":57,"type":22},40,[25],"This randomized controlled superiority trial will compare a 6-week digital health rehabilitation program with a 6-week self-guided exercise program in adults with patellofemoral pain. Assessments will be performed at baseline, 6 weeks, and 18 weeks. The primary outcome will be change in AKPS from baseline to 6 weeks. Secondary outcomes will include pain intensity, self-reported function, psychological outcomes, quality of life, muscle strength, adherence, and adverse events.",[61],"PFPS",[63,64,65],"PFP","rehabilitation","digital health","2026-04-16",{"date":68,"type":39},"2026-04-22",{"date":70,"type":22},"2026-05-15",{"date":72,"type":22},"2027-05-15",{"name":45,"class":46},{"id":75,"slug":76,"hasResults":11,"nctId":77,"briefTitle":78,"officialTitle":79,"acronym":80,"eligibilityCriteria":81,"healthyVolunteers":82,"sex":17,"minAge":18,"maxAge":83,"enrollmentInfo":84,"targetDuration":4,"studyType":23,"phases":86,"briefSummary":87,"conditions":88,"keywords":90,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":92,"lastUpdatePostDateStruct":93,"startDateStruct":95,"completionDateStruct":97,"leadSponsor":99,"locationsCount":4},"100586877","cessation-on-internet-addiction-in-college-students-100586877","NCT06921096","Cessation on Internet Addiction in College Students","Effect of Tai Chi Exercise and Its Cessation on Internet Addiction in College Students: A Randomized Controlled Trial","IAD","Inclusion Criteria:\n\n* Participants aged 18-25;\n* CIAS scores of 26-53 (low internet dependence), 54-80 (moderate dependence), or 81-104 (high dependence). Only mild and moderate cases were included;\n* non-sports majors; the study followed the Declaration of Helsinki, and all participants understood the purpose and signed consent forms.\n\nExclusion Criteria:\n\n* Severe IAD (CIAS score \\>80);\n* Tai Chi practice within 6 months;\n* regular exercise habits;\n* history of depression\u002Fanxiety or undergoing psychological treatment;\n* use of medications affecting mental state or neurotransmitter levels.",true,"25 Years",{"count":85,"type":22},51,[25],"This study aimed to explore the intervention effect of Tai Chi exercise on internet addiction in college students and its maintenance effect after cessation, providing a scientific basis for the application of Tai Chi in internet addiction intervention among college students. Fifty-one non-sports-major college students with mild or moderate internet addiction were randomly divided into a Tai Chi group (n = 23) and a control group (n = 24). The Tai Chi group underwent 12 weeks of Tai Chi exercise, while the control group maintained their regular study schedule without additional physical exercise. The Chinese Internet Addiction Scale and serum dopamine and β-Endorphin levels were assessed at baseline, week 12, and week 16.",[89],"Internet Addiction Disorder",[89,91],"Tai Chi","2025-04-08",{"date":94,"type":39},"2025-04-10",{"date":96,"type":22},"2025-04-15",{"date":98,"type":22},"2025-08-16",{"name":45,"class":46},{"id":101,"slug":102,"hasResults":11,"nctId":103,"briefTitle":104,"officialTitle":104,"acronym":105,"eligibilityCriteria":106,"healthyVolunteers":82,"sex":107,"minAge":108,"maxAge":109,"enrollmentInfo":110,"targetDuration":4,"studyType":23,"phases":112,"briefSummary":113,"conditions":114,"keywords":116,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":118,"lastUpdatePostDateStruct":119,"startDateStruct":121,"completionDateStruct":123,"leadSponsor":124,"locationsCount":4},"100583002","muscle-isometric-contraction-for-the-treatment-of-knee-osteoarthritis-100583002","NCT06870656","Muscle Isometric Contraction for the Treatment of Knee Osteoarthritis","KOA","Inclusion Criteria:\n\n* Women aged 60 to 80 years;\n* Based on the diagnostic criteria for knee osteoarthritis (KOA) established by the American College of Rheumatology in 2001, participants with KOA graded 1 to 3 were selected;\n* Compliance with the Declaration of Helsinki and signing of the informed consent form.\n\nExclusion Criteria:\n\n* Cardiovascular diseases;\n* Need for surgery or pharmacological treatment in the near future;\n* Neuromuscular diseases;\n* Currently engaged in regular exercise.","FEMALE","60 Years","80 Years",{"count":111,"type":22},120,[25],"This study compares the effects of three different intensities of Muscle Isometric Contraction (MIC) on balance ability, proprioception, muscle strength, KOA symptoms, and inflammatory factors in synovial fluid among elderly individuals with Knee Osteoarthritis (KOA).",[115],"Knee Osteoarthritis (Knee OA)",[105,117],"Muscle isometric contraction","2025-03-06",{"date":120,"type":39},"2025-03-11",{"date":122,"type":22},"2025-09-20",{"date":122,"type":22},{"name":45,"class":46},{"id":126,"slug":127,"hasResults":11,"nctId":128,"briefTitle":129,"officialTitle":130,"acronym":131,"eligibilityCriteria":132,"healthyVolunteers":11,"sex":17,"minAge":133,"maxAge":19,"enrollmentInfo":134,"targetDuration":4,"studyType":23,"phases":136,"briefSummary":137,"conditions":138,"keywords":4,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":140,"lastUpdatePostDateStruct":141,"startDateStruct":143,"completionDateStruct":145,"leadSponsor":147,"locationsCount":4},"100574529","development-and-evaluation-of-functional-probiotic-powder-in-human-trials-100574529","NCT06760468","Development and Evaluation of Functional Probiotic Powder in Human Trials","Functional Probiotic Powder Human Trials","FPPHT","Inclusion Criteria:\n\n* Age Range: Individuals aged 20 to 30 years old.\n* Health Status: Healthy, without chronic illnesses or disabilities.\n* Athletic Background: Well-trained athletes with a history of regular physical activity.\n* Lifestyle: No history of smoking or excessive alcohol consumption.\n* Compliance and Consent: Capable of understanding and adhering to study protocols and willing to provide informed consent.\n\nExclusion Criteria:\n\n* Chronic Illnesses: Individuals with unmanaged chronic diseases\n* Substance Use: Current smokers or individuals with a history of substance abuse.\n* Allergies and Supplements: History of food allergies or long-term use of nutritional supplements and medications.\n* Probiotic and Antibiotic Use: Use of probiotics, fermented products, or antibiotics during the study period.\n* Other Conditions: Pregnant or breastfeeding women, individuals with severe mental health conditions, or those participating in other clinical studies.","20 Years",{"count":135,"type":22},60,[25],"Purpose: To optimize the preparation process of probiotic powder and assess its impact on healthy athletes, providing a scientific basis for functional foods.\n\nProcedures:\n\nProbiotic Powder Preparation: Using vacuum freeze-drying to improve bacterial survival rates.\n\nHuman Trials: Recruiting healthy athletes aged 20-30, divided into placebo and probiotic powder groups for an 8-week trial.\n\nTesting and Analysis: Conducting running exhaustion tests and blood biochemical analysis to evaluate the effects of probiotic powder.\n\nImportance: Understanding the effects of probiotics on athletes helps develop better health products.",[139],"Exercise Fatigue","2025-01-03",{"date":142,"type":39},"2025-01-06",{"date":144,"type":22},"2025-02-01",{"date":146,"type":22},"2025-06-01",{"name":45,"class":46},{"id":149,"slug":150,"hasResults":11,"nctId":151,"briefTitle":152,"officialTitle":153,"acronym":4,"eligibilityCriteria":154,"healthyVolunteers":82,"sex":107,"minAge":18,"maxAge":19,"enrollmentInfo":155,"targetDuration":4,"studyType":23,"phases":157,"briefSummary":158,"conditions":159,"keywords":4,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":161,"lastUpdatePostDateStruct":162,"startDateStruct":164,"completionDateStruct":166,"leadSponsor":168,"locationsCount":4},"100558656","athlete-biochemical-monitoring-and-nutritional-support-100558656","NCT06553963","Athlete Biochemical Monitoring and Nutritional Support","Biochemical Monitoring and Nutritional Support During Pre-Competition Weight Reduction in Female Weightlifters: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Age between 18 and 30 years old\n* At least 5 years of professional weightlifting training experience\n* Currently undergoing systematic training\n* Passed a health examination\n* The study complies with the Declaration of Helsinki and signed an informed consent form.\n\nExclusion Criteria:\n\n* Obvious injuries to the lower limb joints\n* Taking prescription medications (such as those affecting mood and sleep)\n* Abnormal cardiovascular function.",{"count":156,"type":22},28,[25],"The objective of this study is to evaluate the efficacy of physiological and biochemical monitoring along with nutritional support in improving the performance and well-being of female weightlifters during the critical weight reduction phase before competition. It also seeks to determine the safety and potential benefits of the personalized nutritional interventions.\n\nThe primary questions this study aims to address are:\n\nDoes personalized nutritional support, informed by physiological and biochemical monitoring, reduce the incidence of fatigue and improve sleep quality in female weightlifters during the pre-competition period? How do serum indicators change in response to the nutritional interventions, and what does this indicate about the athletes' health and performance? What are the perceived benefits and any potential adverse effects reported by the participants receiving the nutritional support? To assess the impact of the intervention, researchers will compare the outcomes of the experimental group, which receives the tailored nutritional support, to those of the control group, which follows standard practices without additional intervention.\n\nParticipants will be required to:\n\nConsume the nutritional supplements or maintain their regular diet as assigned for the duration of the 1-month study.\n\nAttend scheduled visits to the research facility every two weeks for comprehensive health assessments, including blood tests for serum indicators and evaluations of fatigue levels and PSQI scores.\n\nRecord their daily experiences, including dietary adherence, training intensity, perceived fatigue, sleep patterns, and any other relevant observations in a personal diary.\n\nBy conducting this randomized controlled trial, the study will provide valuable insights into the role of targeted nutritional support in enhancing athletic performance and overall health during the demanding pre-competition weight reduction period.",[160],"Weight Reduction","2024-08-14",{"date":163,"type":39},"2024-08-16",{"date":165,"type":22},"2024-08-20",{"date":167,"type":22},"2024-09-20",{"name":45,"class":46},{"id":170,"slug":171,"hasResults":11,"nctId":172,"briefTitle":173,"officialTitle":174,"acronym":175,"eligibilityCriteria":176,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":177,"targetDuration":4,"studyType":23,"phases":179,"briefSummary":180,"conditions":181,"keywords":183,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":184,"lastUpdatePostDateStruct":185,"startDateStruct":187,"completionDateStruct":188,"leadSponsor":190,"locationsCount":4},"100557223","delayed-onset-muscle-soreness-of-athletes-100557223","NCT06535321","Delayed Onset Muscle Soreness of Athletes","Effects of Vibration Training Combined With Kinesio Taping on Delayed Onset Muscle Soreness of Athletes' Knee Joints: A Randomised Controlled Trial","DOMS","Inclusion Criteria:\n\n* Athletes who performed regular training, ranked in the top 3 in a provincial competition and trained at least 5days per week, with a minimum of 4 h each day.\n* This training encompassed, but was not limited to, strength training, endurance training, skill drills and competitive preparation.\n* This study was in line with the Declaration of Helsinki, and the participants were aware of the study intention and signed informed consent.\n\nExclusion Criteria:\n\n* Lower limb joint injury and systematic exercise training in the last week.",{"count":178,"type":22},45,[25],"Study Design:\n\nThis study was approved by the Human Experiment Ethics Committee of Chengdu Sport University (No: 2103).\n\nBased on previous research data, G-power software was used to calculate that at least 40 samples were needed.\n\nParticipants:\n\nA total of 45 track and field athletes from Sichuan Province, China, were recruited during the off-season in 2024. They were randomly assigned to the vibration group, kinesio taping group, combined group, and control group.\n\nAll participants signed informed consent forms and adhered to the Declaration of Helsinki.\n\nDOMS Modeling:\n\nFollowing previous research, a delayed onset muscle soreness (DOMS) model for athletes\\' knee joints was established through downhill running.\n\nDetailed oxygen uptake tests were conducted on all participants one week before DOMS modeling, and records were made one week after DOMS modeling.\n\nIntervention Measures:\n\nThe vibration group received vibration training immediately after DOMS modeling.\n\nThe kinesio taping group had Y-shaped kinesio taping applied 30 minutes before DOMS modeling.\n\nThe combined group received both vibration training and kinesio taping simultaneously.\n\nAssessment Methods:\n\nThe degree of pain at the DOMS site for participants was evaluated using a Visual Analogue Scale (VAS).\n\nThe concentration of creatine kinase (CK) in the serum of participants was detected using an RT-9600 automatic biochemical analyzer, and serum interleukin-6 (IL-6) was detected by enzyme-linked immunosorbent assay (ELISA).\n\nAn IsoMed 2000 isokinetic tester was used to perform a 60°\u002Fs extension test on the participants\\' knees.\n\nData Collection:\n\nVAS scores, serum CK and IL-6 levels, and peak torque of knee extension were collected at different time points before and after DOMS modeling.",[182],"Delayed Onset Muscle Soreness",[182],"2024-08-01",{"date":186,"type":39},"2024-08-02",{"date":165,"type":22},{"date":189,"type":22},"2024-09-15",{"name":45,"class":46},{"id":192,"slug":193,"hasResults":11,"nctId":194,"briefTitle":195,"officialTitle":196,"acronym":4,"eligibilityCriteria":197,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":108,"enrollmentInfo":198,"targetDuration":4,"studyType":23,"phases":200,"briefSummary":201,"conditions":202,"keywords":205,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":209,"lastUpdatePostDateStruct":210,"startDateStruct":212,"completionDateStruct":214,"leadSponsor":216,"locationsCount":4},"100545267","resonance-breathing-training-for-long-covid-related-myocardial-injury-100545267","NCT06379672","Resonance Breathing Training for Long Covid-related Myocardial Injury","An Investigation of the Efficacy of Resonance Breathing Training in the Rehabilitation of Patients with Long Covid-related Myocardial Injury","Inclusion Criteria:\n\n1. Age between 18 and 60 years;\n2. According to the WHO definition: one or more systemic involvement present 3 months after the diagnosis of a new crown infection, and at least 2 of these months cannot be explained by other diseases\n3. 2D-STE suggestive of GLSAVG: -17% ≤ men ≤ -10%, -18% ≤ women ≤ -10%;\n4. Consent for enrollment based on the degree of myocardial injury, as diagnosed by a clinician;\n5. Signing the informed consent form with the consent of the patient or his\u002Fher family members\n\nExclusion Criteria:\n\n* (1) Previous history of coronary atherosclerotic heart disease and heart failure; (2) Combination of severe arrhythmia or cardiogenic shock; (3) Combination of severe hypertension, hypertrophic cardiomyopathy, valvular disease of moderate or higher grade, acute myocarditis or pericarditis; (4) Combination of any disease that severely affects limb movement, such as musculoskeletal system disease or severe hepatic or renal insufficiency; (5) Combination of progressive malignant tumors, infectious diseases, bleeding disorders, autoimmune diseases, etc; Those who have serious mental illness and are unable to cooperate",{"count":199,"type":22},70,[25],"An investigation of the efficacy of resonance breathing training in the rehabilitation of patients with Long covid-related myocardial injury",[203,204],"Long COVID","Myocardial Injury",[206,207,204,208],"2D-STE","resonance breathing","Long Covid-19","2024-07-29",{"date":211,"type":39},"2024-07-30",{"date":213,"type":22},"2024-08-25",{"date":215,"type":22},"2024-10-05",{"name":45,"class":46},""]