[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"peloidotherapy\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:peloidotherapy":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,46,81],{"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":22,"studyType":23,"phases":4,"briefSummary":24,"conditions":25,"keywords":29,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":34,"lastUpdatePostDateStruct":35,"startDateStruct":38,"completionDateStruct":40,"leadSponsor":42,"locationsCount":45},"100628266","the-effect-of-peloidotherapy-in-young-adults-undergoing-physical-therapy-scoliosis-specific-exercises-psse-100628266",false,"NCT07459400","The Effect of Peloidotherapy in Young Adults Undergoing Physical Therapy Scoliosis Specific Exercises (PSSE)","The Effect of Peloidotherapy on Pain and Quality of Life in Young Adult Individuals With Scoliosis Undergoing Physiotherapy Scoliosis-Specific Exercises (PSSE)","Inclusion Criteria:\n\n* Aged 20-40 years\n* Diagnosed with idiopathic scoliosis by a specialist physician\n* Cobb angle between 15-40 degrees\n* Able to perform PSSE exercises throughout the study period\n* VAS ≥3 at the start of the study\n* Has had pain complaints for at least 3 months\n* Individuals who have agreed in writing to participate in the study\n\nExclusion Criteria:\n\n* Individuals who have undergone scoliosis surgery\n* Individuals with neuromuscular, congenital, or secondary scoliosis\n* Individuals with rheumatological, inflammatory, or serious chronic diseases (such as cardiopulmonary insufficiency or kidney disease)\n* Pregnant and breastfeeding women\n* Conditions in which peloidotherapy is contraindicated (active skin infection, open wound, serious dermatological disease, history of allergic reaction, severe cardiopulmonary, kidney or liver failure, bleeding disorder or anticoagulant use, pregnancy\u002Fbreastfeeding, and systemic infection)\n* Individuals with serious psychiatric disorders that may interfere with treatment compliance or affect consent\n* Individuals receiving additional physical therapy during the study period","ALL","20 Years","40 Years",{"count":20,"type":21},54,"ESTIMATED","4 Months","OBSERVATIONAL","Scoliosis is a musculoskeletal disorder defined by a three-dimensional spinal deformity that can result in substantial clinical and functional limitations, particularly during adolescence and young adulthood. Affected individuals commonly experience postural asymmetry, muscular imbalance, pain, and diminished quality of life. In conservative management, Physiotherapeutic Scoliosis-Specific Exercises (PSSE) have gained recognition as a fundamental intervention. The primary objectives of PSSE include optimizing spinal alignment, facilitating rotational breathing, and restoring muscular symmetry to improve functional capacity. Evidence from systematic reviews suggests that PSSE, especially the Schroth method, are superior to general exercise programs in improving both radiographic parameters and health-related quality of life.Meta-analytic findings further support the effectiveness of PSSE in reducing curve magnitude and enhancing quality of life outcomes. Among the various PSSE approaches, the Schroth method is one of the most extensively investigated and widely applied in clinical settings. This method incorporates three-dimensional postural correction, targeted breathing techniques, and the development of postural awareness. Randomized controlled trials have demonstrated that Schroth exercises significantly improve SRS-22 quality of life scores and positively influence pain, body image, and overall well-being.Despite these established benefits, pain and muscle tension occurring during exercise sessions may negatively influence adherence to rehabilitation programs. In young adults, pain is a critical factor limiting treatment compliance and restricting engagement in daily activities. Accordingly, adjunctive interventions implemented prior to exercise may enhance exercise tolerance and optimize therapeutic outcomes.Peloidotherapy, which involves the therapeutic application of natural medicinal mud, is commonly used in musculoskeletal rehabilitation due to its analgesic, muscle-relaxant, and circulation-enhancing effects. By alleviating pain and reducing muscular tension, peloidotherapy may facilitate greater participation in exercise programs and support improved clinical outcomes.This study aims to investigate the effects of adjunctive peloidotherapy administered before Schroth-based PSSE in young adults with scoliosis, focusing on pain, exercise adherence, and quality of life, with particular emphasis on SRS-22 measures..",[26,27,28],"Spine Deformity","Adult Scoliosis","Peloidotherapy",[28,27,30,31,32],"Physiotherapy Scoliosis-Specific Exercises (PSSE)","Pain","Quality of Life","RECRUITING","2026-06-08",{"date":36,"type":37},"2026-06-10","ACTUAL",{"date":39,"type":37},"2026-03-23",{"date":41,"type":21},"2026-10-23",{"name":43,"class":44},"Gaziosmanpasa Research and Education Hospital","OTHER_GOV",1,{"id":47,"slug":48,"hasResults":11,"nctId":49,"briefTitle":50,"officialTitle":51,"acronym":4,"eligibilityCriteria":52,"healthyVolunteers":11,"sex":16,"minAge":53,"maxAge":54,"enrollmentInfo":55,"targetDuration":4,"studyType":57,"phases":58,"briefSummary":60,"conditions":61,"keywords":66,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":72,"lastUpdatePostDateStruct":73,"startDateStruct":75,"completionDateStruct":77,"leadSponsor":79,"locationsCount":45},"100591199","effectiveness-of-kinesiotaping-and-peloidotherapy-in-carpal-tunnel-syndrome-100591199","NCT06977321","Effectiveness of Kinesiotaping and Peloidotherapy in Carpal Tunnel Syndrome","A Comparative Evaluation of the Effectiveness of Kinesiotaping and Peloidotherapy in Patients With Idiopathic Carpal Tunnel Syndrome","Inclusion Criteria:\n\n* Being between the ages of 18-65\n* Agreeing to participate voluntarily in the study\n* Being diagnosed with mild or moderate idiopathic chronic CTS as a result of anamnesis, clinical examination and nerve conduction study\n\nExclusion Criteria:\n\n* Presence of predisposing etiological factors for CTS such as diabetes mellitus, chronic kidney and liver disease, acromegaly, rheumatological diseases, acute trauma, hypothyroidism, etc.\n* Being diagnosed with severe CTS\n* Having a history of previous wrist surgery or trauma\n* Having atrophy in the thenar region or weakness in the thenar muscles\n* Having cervical radiculopathy, thoracic outlet syndrome, polyneuropathy, brachial neuropathy or proximal median nerve neuropathy\n* Having had steroid injections in the last 3 months and taking oral steroid medications\n* Being pregnant\n* Having an open wound or rash in the wrist and its surroundings that would prevent treatment\n* Patients who are receiving or will receive another\u002Fadditional treatment for CTS\n* Patients with a bifid median nerve, persistent median artery, ganglion cyst, tenosynovitis, or tendinitis in the wrist.","18 Months","65 Months",{"count":56,"type":21},90,"INTERVENTIONAL",[59],"NA","Patients diagnosed with mild and moderate idiopathic CTS will be randomly divided into three groups. Patients who received 15 sessions of peloid therapy along with a home exercise program will constitute the first group. The second group will consist of patients who received a total of 6 sessions of kinesiotaping twice a week along with a home exercise program. Patients who were given only a home exercise program will be included in the third group. \"Patients will be evaluated in detail in terms of clinical examination and outcomes three weeks after the end of treatment and again at three months.",[62,63,64,65,28],"Carpal Tunnel Syndrome (CTS)","Kinesio Taping","Exercise","Pain Management",[67,28,68,69,70,71],"carpal tunnel syndrome (CTS)","exercise","pain","kinesio taping","ultrasound","2026-03-19",{"date":74,"type":37},"2026-03-20",{"date":76,"type":37},"2025-05-17",{"date":78,"type":21},"2026-05-15",{"name":80,"class":44},"Konya Beyhekim Training and Research Hospital",{"id":82,"slug":83,"hasResults":11,"nctId":84,"briefTitle":85,"officialTitle":86,"acronym":4,"eligibilityCriteria":87,"healthyVolunteers":11,"sex":16,"minAge":88,"maxAge":89,"enrollmentInfo":90,"targetDuration":4,"studyType":57,"phases":92,"briefSummary":93,"conditions":94,"keywords":100,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":106,"lastUpdatePostDateStruct":107,"startDateStruct":108,"completionDateStruct":110,"leadSponsor":112,"locationsCount":45},"100612664","comparative-evaluation-of-finger-splint-paraffin-and-peloidotherapy-interventions-in-the-management-of-trigger-finger-100612664","NCT07256522","Comparative Evaluation of Finger Splint, Paraffin, and Peloidotherapy Interventions in the Management of Trigger Finger","Comparative Evaluation of Finger Splint, Paraffin, and Peloidotherapy Interventions in the Management of Trigger Finger. A Prospective, Randomized, Controlled Study","Inclusion Criteria:\n\n* Being between 18 and 75 years of age and willing to participate in the study\n* Having a diagnosis of idiopathic single trigger finger, Grade 2-3\n\nExclusion Criteria:\n\n* Patients with triggering in more than one finger\n* Patients with triggering at the A3 pulley or with Grade 1 or Grade 4 trigger finger\n* Patients with thumb (pollex) trigger finger\n* Patients who have undergone any injection or interventional procedure (release surgery) for trigger finger within the past 6 months\n* Patients who have received physical therapy for the hand within the past 6 months\n* Patients currently using corticosteroids or nonsteroidal anti-inflammatory drugs (NSAIDs)\n* Patients with inflammatory or autoimmune rheumatologic diseases such as rheumatoid arthritis, systemic lupus erythematosus, gout, or psoriatic arthritis\n* Patients with other musculoskeletal disorders (e.g., carpal tunnel syndrome, de Quervain's tenosynovitis, symptomatic hand osteoarthritis, or Dupuytren's contracture) or neurological diseases (e.g., stroke-related hemiparesis, spinal cord injury, brachial plexus injury, multiple sclerosis, or Parkinsonism) affecting the same hand\n* Patients with musculoskeletal disorders causing pain and\u002For limitation in the proximal upper extremity on the affected side (e.g., periarthritis, lateral epicondylitis, mononeuropathy, or radiculopathy)\n* Patients with significant metabolic diseases (e.g., hypothyroidism, Cushing's syndrome, or uncontrolled diabetes)\n* Patients with any condition that may interfere with treatment, such as open wounds, rashes, local infections, or active malignant disease of the hand\n* Patients with a history of hand trauma (chronic or repetitive)\n* Patients unwilling to complete the self-assessment questionnaires either independently or with assistance\n* Pregnant women","18 Years","75 Years",{"count":91,"type":21},60,[59],"Patients aged 18-75 years who present with trigger finger to a tertiary rehabilitation hospital and agree to participate will be included in the study. Participants will be randomly allocated into three groups using block randomization. The first group will use a static finger splint that blocks the proximal interphalangeal joint for 6 weeks, along with a home exercise program. The second group will receive paraffin bath therapy, and the third group will receive peloidotherapy, both in combination with home exercises.\n\nAll patients will receive education about the disease and activity modification. The finger joint-restricting splint and exercises will be applied for 6 weeks. Evaluations will be conducted at baseline, at the end of the 3rd week, and at the end of the 6th week by a blinded assessor. No analgesic or anti-inflammatory medication will be permitted during the study, and patients will be instructed to avoid using analgesics within 24 hours prior to each assessment.",[95,96,97,28,98,99],"Trigger Finger","Splint Therapy","Paraffin Bath","Efficacy and Safety","Randomised Clinical Trial",[101,102,103,104,105],"trigger finger","splint therapy","paraffin bath","peloidotherapy","Randomised Controlled Study","2026-03-17",{"date":72,"type":37},{"date":109,"type":37},"2025-12-15",{"date":111,"type":21},"2027-02-15",{"name":80,"class":44}]