[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100648775":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":25,"centralContacts":29,"locations":38,"responsibleParty":54,"collaborators":18,"id":57,"slug":58,"hasResults":59,"nctId":60,"briefTitle":61,"officialTitle":62,"acronym":18,"eligibilityCriteria":63,"healthyVolunteers":59,"sex":64,"minAge":65,"maxAge":66,"enrollmentInfo":67,"targetDuration":18,"studyType":70,"phases":71,"briefSummary":73,"conditions":74,"keywords":76,"overallStatus":83,"whyStopped":18,"lastUpdateSubmitDate":84,"lastUpdatePostDateStruct":85,"startDateStruct":88,"completionDateStruct":90,"leadSponsor":92,"locationsCount":93},{"fullName":5,"class":6},"Pusan National University Yangsan Hospital","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Exercise group","EXPERIMENTAL","Participants will receive a supervised upper-limb resistance training program three times per week for 8 weeks. The program consists of progressive resistance exercises for the upper extremities.",[13],"Behavioral: Upper-Limb Resistance Training",{"label":15,"type":16,"description":17,"interventionNames":18},"Control group","NO_INTERVENTION","Participants will continue their usual daily activities without participating in the resistance training program during the 8-week study period.",null,[20],{"type":21,"name":22,"description":23,"armGroupLabels":24,"otherNames":18},"BEHAVIORAL","Upper-Limb Resistance Training","Participants will perform a supervised upper-limb resistance training program three times per week for 8 weeks. Each session will last approximately 30 minutes and consist of progressive resistance exercises for the upper extremities. Exercise intensity will be progressively adjusted according to each participant's tolerance.",[9],[26],{"name":27,"affiliation":5,"role":28},"Sungchul Huh, MD, PhD","PRINCIPAL_INVESTIGATOR",[30,35],{"name":31,"role":32,"phone":33,"phoneExt":18,"email":34},"Dogyu Lee, M.S.","CONTACT","055-360-1730","2doq2doq@gmail.com",{"name":36,"role":32,"phone":33,"phoneExt":18,"email":37},"Yuna Kim, B.S.","kyoona1289@gmail.com",[39],{"facility":5,"status":18,"city":40,"state":41,"zip":42,"country":43,"countryCode":18,"cosmosGeoPoint":44,"geoPoint":49,"contacts":50},"Yangsan","Gyeongsangnam-do","50612","South Korea",{"type":45,"coordinates":46},"Point",[47,48],129.03358,35.34199,{"lat":48,"lon":47},[51,52,53],{"name":31,"role":32,"phone":33,"phoneExt":18,"email":34},{"name":36,"role":32,"phone":33,"phoneExt":18,"email":37},{"name":27,"role":28,"phone":18,"phoneExt":18,"email":18},{"type":28,"investigatorFullName":55,"investigatorTitle":56,"investigatorAffiliation":5,"oldNameTitle":18,"oldOrganization":18},"Sungchul Huh","Assistant professor","100648775","cardiovascular-autonomic-function-after-resistance-training-100648775",false,"NCT07725952","Cardiovascular Autonomic Function After Resistance Training","Effects of 8-Week Resistance Training on Cardiovascular Autonomic Function in Spinal Cord Injury","Inclusion Criteria:\n\n* Provided written informed consent and agreed to participate in the study.\n* Adults aged 19 to 85 years.\n* Chronic spinal cord injury (SCI) of traumatic or non-traumatic etiology, at least 6 months after injury.\n* Cervical or thoracic spinal cord injury.\n* Classified as American Spinal Injury Association (ASIA) Impairment Scale (AIS) grade A, B, C, or D.\n* Sufficient upper-limb range of motion to perform resistance training.\n* Elbow extensor muscle strength of Manual Muscle Test (MMT) grade 3 or higher.\n\nExclusion Criteria:\n\n* Presence of any serious medical condition that would preclude participation in the study.\n* Inability to understand or perform the exercise program.\n* Uncontrolled diabetes mellitus or progressive neurological disease.\n* Uncontrolled hypertension (systolic blood pressure \\>140 mmHg or diastolic blood pressure \\>90 mmHg).\n* History of cardiovascular disease within the past 6 months.\n* Current use of medications that may affect heart rate variability (HRV) or baroreflex sensitivity (BRS).\n* Severe orthostatic hypotension (OH) or autonomic dysreflexia (AD).\n* Considered unsuitable for participation in the study by a board-certified specialist in Physical and Rehabilitation Medicine.","ALL","19 Years","85 Years",{"count":68,"type":69},20,"ESTIMATED","INTERVENTIONAL",[72],"NA","The purpose of this clinical trial is to evaluate whether an 8-week upper-limb resistance training program improves cardiovascular autonomic function in adults with chronic spinal cord injury (SCI). The primary objectives are to determine whether upper-limb resistance training improves heart rate variability (HRV) and baroreflex sensitivity (BRS), and whether it improves blood pressure responses during postural change, upper-limb strength, symptoms related to orthostatic hypotension, and quality of life.\n\nParticipants will be randomly assigned to either the resistance training group or the control group. All participants will complete assessments before and after the 8-week study period, including measurements of HRV, BRS, blood pressure responses during a tilt-table test, hand grip strength, and questionnaires assessing orthostatic hypotension symptoms and quality of life. Participants assigned to the resistance training group will participate in supervised upper-limb resistance training three times per week for 8 weeks.",[75],"Spinal Cord Injury",[75,77,78,79,80,81,82],"Resistance Training","Cardiovascular Autonomic Function","Heart Rate Variability","Baroreflex Sensitivity","Orthostatic Hypotension","Exercise Rehabilitation","NOT_YET_RECRUITING","2026-07-21",{"date":86,"type":87},"2026-07-24","ACTUAL",{"date":89,"type":69},"2026-07-27",{"date":91,"type":69},"2026-12-31",{"name":5,"class":6},1]