[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"thoracic-outlet-syndrome\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:thoracic-outlet-syndrome":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,47,72,109],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":28,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":35,"lastUpdatePostDateStruct":36,"startDateStruct":39,"completionDateStruct":41,"leadSponsor":43,"locationsCount":46},"100643893","motivational-interviewing-in-thoracic-outlet-syndrome-100643893",false,"NCT07668206","Motivational Interviewing in Thoracic Outlet Syndrome","The Effect of Motivational Interviewing on Thoracic Outlet Syndrome Symptoms in Patients With Thoracic Outlet Syndrome","Inclusion Criteria:\n\n* Diagnosis of thoracic outlet syndrome\n* Age between 18 and 65 years\n* Pain duration of more than 6 months\n* No surgical intervention in the last 6 months\n\nExclusion Criteria:\n\n* Accompanying pathologies (cervical disc problems, fibromyalgia, rotator cuff problems, diabetes, neoplastic processes)\n* Unwillingness to provide informed consent","ALL","18 Years","65 Years",{"count":20,"type":21},70,"ESTIMATED","INTERVENTIONAL",[24],"NA","The goal of this clinical trial is to learn if motivational interviewing (MI) works to improve symptoms in people with thoracic outlet syndrome (TOS). TOS is a condition that causes long-term pain, numbness, and weakness in the arm and shoulder area. The main questions it aims to answer are:\n\n* Does MI lower pain and improve arm function in people with TOS?\n* Does psychological resilience predict treatment outcomes in people with TOS? Researchers will compare participants who receive MI sessions plus a home exercise program to those who receive a home exercise program alone. Participants will be randomly assigned to one of the two groups.\n\nParticipants will:\n\n* Follow a home exercise program for 6 weeks\n* Some participants will also attend up to 4 motivational interviewing sessions\n* Complete questionnaires about pain, function, sleep, anxiety, and depression at the start and end of the 6-week program",[27],"Thoracic Outlet Syndrome",[29,30,31,32,33,27],"Motivational Interviewing","Chronic Pain","Home Exercise Program","Psychological Resilience","Central Sensitization","NOT_YET_RECRUITING","2026-06-19",{"date":37,"type":38},"2026-06-25","ACTUAL",{"date":40,"type":21},"2026-06",{"date":42,"type":21},"2027-10",{"name":44,"class":45},"Hacettepe University","OTHER",1,{"id":48,"slug":49,"hasResults":11,"nctId":50,"briefTitle":51,"officialTitle":51,"acronym":52,"eligibilityCriteria":53,"healthyVolunteers":11,"sex":16,"minAge":54,"maxAge":55,"enrollmentInfo":56,"targetDuration":4,"studyType":22,"phases":58,"briefSummary":59,"conditions":60,"keywords":61,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":63,"lastUpdatePostDateStruct":64,"startDateStruct":66,"completionDateStruct":68,"leadSponsor":70,"locationsCount":4},"100634143","effect-of-low-power-laser-therapy-on-pain-and-functional-outcomes-in-patients-with-thoracic-outlet-syndrome-100634143","NCT07535853","Effect of Low-Power Laser Therapy on Pain and Functional Outcomes in Patients With Thoracic Outlet Syndrome","LPLT-TOS","Inclusion Criteria:\n\n* Age\n\nInclusion Criteria:\n\n* Age between 35-50 years.\n* Clinically diagnosed with Thoracic Outlet Syndrome (TOS) by a physician based on standard diagnostic criteria.\n* Presence of neurogenic symptoms such as pain, paraesthesia, numbness, or --\n* weakness in the upper extremity.\n* Symptoms lasting for at least 3 months.\n\nExclusion Criteria:\n\n* History of cervical disc herniation or cervical radiculopathy.\n* Previous surgical intervention in the cervical or thoracic outlet region.\n* Severe cardiovascular or systemic diseases that may interfere with treatment. --Pacemakers or other implanted electronic devices.\n* Skin conditions or infections in the treatment area.\n* Receiving any other form of laser therapy or conflicting treatment during the study.","30 Years","50 Years",{"count":57,"type":21},40,[24],"The purpose of this study is to evaluate the effect of low-power laser therapy on pain intensity and functional outcomes in patients diagnosed with Thoracic Outlet Syndrome (TOS). Participants will be randomly assigned to either receive the active laser therapy combined with a physical therapy program or a control group. The study aims to determine if adding laser therapy provides better relief and improves daily physical functions compared to conventional treatment alone.",[27],[62],"LPLT","2026-04-10",{"date":65,"type":38},"2026-04-17",{"date":67,"type":21},"2026-04-20",{"date":69,"type":21},"2026-07-17",{"name":71,"class":45},"Cairo University",{"id":73,"slug":74,"hasResults":11,"nctId":75,"briefTitle":76,"officialTitle":77,"acronym":4,"eligibilityCriteria":78,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":79,"targetDuration":4,"studyType":81,"phases":4,"briefSummary":82,"conditions":83,"keywords":4,"overallStatus":99,"whyStopped":4,"lastUpdateSubmitDate":100,"lastUpdatePostDateStruct":101,"startDateStruct":103,"completionDateStruct":105,"leadSponsor":107,"locationsCount":46},"100487581","vascular-lab-resource-vlr-biorepository-100487581","NCT05628948","Vascular Lab Resource (VLR) Biorepository","Vascular Lab Resource (VLR) Biorepository Study","Inclusion Criteria:\n\n1. 18 years or older\n2. Subjects capable of providing informed consent document\n3. Subjects with diagnosed with or at risk for cardiovascular and metabolic diseases\n\nExclusion Criteria:\n\n1. Known life expectancy of ≤ 6 months at the time of enrollment\n2. Known current pregnancy\n3. Severe Anemia (last documented hemoglobin \\\u003C 7.0 g\u002FdL)",{"count":80,"type":21},500,"OBSERVATIONAL","This is a study of biomarkers obtained from prospectively collected subject samples and their correlation with cardiovascular and metabolic diseases. The purpose of this initiative is to develop an enduring tool to allow for collaborative research between clinicians at Cleveland Clinic Main Campus and basic scientists at the Lerner Research Institute. This collaboration will allow resources to be available to clinical and basic researchers alike. This tool will enable research of vascular disease in the Vascular Lab and will leverage this valuable asset to the fullest extent to allow for interdepartmental collaboration.",[84,85,86,87,88,89,90,91,92,93,94,95,96,97,27,98],"Cardiovascular Diseases","Metabolic Disease","Peripheral Artery Disease","Carotid Disease","Aneurysmal Disease","Venous Disease","Thrombosis","Lymphedema","Lipedema","Non-Atherosclerotic Chronic Arterial Occlusive Disease","Vasculitis","Fibromuscular Dysplasia","Arterial Dissection","May-Thurner Syndrome","Vasospasm","RECRUITING","2025-12-15",{"date":102,"type":38},"2025-12-19",{"date":104,"type":38},"2019-11-14",{"date":106,"type":21},"2031-06-30",{"name":108,"class":45},"The Cleveland Clinic",{"id":110,"slug":111,"hasResults":11,"nctId":112,"briefTitle":113,"officialTitle":114,"acronym":4,"eligibilityCriteria":115,"healthyVolunteers":116,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":117,"targetDuration":4,"studyType":81,"phases":4,"briefSummary":119,"conditions":120,"keywords":121,"overallStatus":99,"whyStopped":4,"lastUpdateSubmitDate":123,"lastUpdatePostDateStruct":124,"startDateStruct":126,"completionDateStruct":128,"leadSponsor":130,"locationsCount":46},"100592386","dysfunctional-breathing-in-individuals-with-thoracic-outlet-syndrome-100592386","NCT06992752","Dysfunctional Breathing in Individuals With Thoracic Outlet Syndrome","Investigation of the Properties of Dysfunctional Breathing in Individuals With Thoracic Outlet Syndrome","Inclusion Criteria:\n\n* To agree to participate in the study,\n* To have been diagnosed with TOS by a thoracic surgeon,\n* To be between 18-65 years old,\n* Having pain for more than 6 months\n\nExclusion Criteria:\n\n* Patients with a history of spinal or thoracic surgery for TOS or any other reason,\n* People with traumatic cervical injury,\n* Severely obese people (BMI \\>40 kg\u002Fm2),\n* People with clinical abnormalities in the thoracic cage or vertebral column,\n* Persons with occupational industrial exposures,\n* Patients with severe comorbidities (neurological, neuromuscular, -cardiorespiratory, psychiatric and musculoskeletal) diabetes mellitus and\u002For malignancies",true,{"count":118,"type":21},54,"The aim of this observational study was to learn about the characteristics of dysfunctional breathing in individuals with thoracic outlet syndrome. The main question to be answered is:\n\nIs there a dysfunctional breathing pattern in individuals with Thoracic outlet syndrome? These features will be compared with a healthy control group to evaluate the association of Thoracic outlet syndrome with dysfunctional breathing",[27],[27,122],"Dysfunctional Breathing","2025-05-22",{"date":125,"type":38},"2025-05-28",{"date":127,"type":38},"2025-02-02",{"date":129,"type":21},"2025-10-02",{"name":44,"class":45}]