[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100608566":3},{"organization":4,"armGroups":7,"interventions":25,"overallOfficials":41,"centralContacts":45,"locations":52,"responsibleParty":68,"collaborators":31,"id":72,"slug":73,"hasResults":74,"nctId":75,"briefTitle":76,"officialTitle":77,"acronym":31,"eligibilityCriteria":78,"healthyVolunteers":74,"sex":79,"minAge":80,"maxAge":81,"enrollmentInfo":82,"targetDuration":31,"studyType":85,"phases":86,"briefSummary":88,"conditions":89,"keywords":91,"overallStatus":54,"whyStopped":31,"lastUpdateSubmitDate":96,"lastUpdatePostDateStruct":97,"startDateStruct":100,"completionDateStruct":102,"leadSponsor":104,"locationsCount":105},{"fullName":5,"class":6},"Ankara Etlik City Hospital","OTHER_GOV",[8,15,21],{"label":9,"type":10,"description":11,"interventionNames":12},"Low Dose Laser Group","EXPERIMENTAL","Patients who will undergo low laser therapy",[13,14],"Device: Low Dose Laser","Other: Conventional physical therapy",{"label":16,"type":17,"description":18,"interventionNames":19},"TENS group","ACTIVE_COMPARATOR","Patients who will undergo TENS therapy",[20,14],"Device: TENS",{"label":22,"type":17,"description":23,"interventionNames":24},"Conventional Therapy","Patients who will undergo conventional therapy",[14],[26,32,36],{"type":27,"name":28,"description":29,"armGroupLabels":30,"otherNames":31},"DEVICE","Low Dose Laser","Patients with subacromial-subdeltoid bursa, m. deltoideus, m. biceps longus, m. infraspinatus, and m. supraspinatus muscles (at the most painful point of the muscles) with a 13-diode Gallium-Aluminium-Arsenide laser device (Intelect Mobile Laser) with a wavelength of 850 nm and 50 mW, 4 Joules per day, 20 seconds, for a total of 15 laser sessions.",[9],null,{"type":27,"name":33,"description":34,"armGroupLabels":35,"otherNames":31},"TENS","TENS therapy will be administered using the TENS device (Intelect Advanced Therapy System) for a total of 15 sessions, 5 days a week, 20 minutes per day, at a dose of 20-40 mA.",[16],{"type":37,"name":38,"description":39,"armGroupLabels":40,"otherNames":31},"OTHER","Conventional physical therapy","Only conventional physiotherapy is planned to be administered to patients.",[22,9,16],[42],{"name":43,"affiliation":5,"role":44},"nihal tezel, associate professor","STUDY_DIRECTOR",[46],{"name":47,"role":48,"phone":49,"phoneExt":50,"email":51},"Aliye Aygün, specialist","CONTACT","+90 0312 797 00 00","+903122911000","aliyeaygunn@hotmail.com",[53],{"facility":5,"status":54,"city":55,"state":56,"zip":57,"country":58,"countryCode":31,"cosmosGeoPoint":59,"geoPoint":64,"contacts":65},"RECRUITING","Ankara","Yenimahalle","06010","Turkey (Türkiye)",{"type":60,"coordinates":61},"Point",[62,63],32.85427,39.91987,{"lat":63,"lon":62},[66],{"name":67,"role":48,"phone":49,"phoneExt":31,"email":51},"Aliye Aygün",{"type":69,"investigatorFullName":70,"investigatorTitle":71,"investigatorAffiliation":5,"oldNameTitle":31,"oldOrganization":31},"PRINCIPAL_INVESTIGATOR","Ayse Naz Kalem","PM&R Specialist","100608566","comparison-of-effectiveness-of-low-dose-laser-and-transcutaneous-electrical-stimulation-in-hemiplegic-shoulder-100608566",false,"NCT07203222","Comparison of Effectiveness of Low Dose Laser and Transcutaneous Electrical Stimulation in Hemiplegic Shoulder","Comparison of the Efficacy of Low-Dose Laser and Transcutaneous Electrical Nerve Stimulation in Subacute Hemiplegic Shoulder Pain, and the Effect of Treatments on Upper Extremity Function and Quality of Life","Inclusion Criteria:\n\n* Patients aged 18-75 years\n* Patients with shoulder pain on the hemiplegic side \\*Mini mental state examination ≥ 25\n* History of stroke within the last 2 weeks to 6 months\n* Patients with shoulder pain scoring 40-100 points on the visual analogue scale (moderate to severe) will be included.\n\nExclusion Criteria:\n\n* Patients who refuse to provide written consent or attend follow-up visits\n* Being under 18 years of age\n* Patients with motor aphasia\n* Patients who have had a shoulder injection within the last 3 months\n* Patients who have undergone upper extremity botulinum toxin application within the last 6 months\n\n  \\*Pregnant women or those planning to become pregnant\n* Inflammatory rheumatic disease\n* Patients who have undergone shoulder injury and surgery prior to stroke\n* Patients with other conditions that could explain shoulder pain\n* Patients with complex regional pain syndrome\n* Patients with a history of epilepsy, pacemaker, or arrhythmia diagnosis\n* Malignancy\n* Diseases such as Alzheimer's or dementia that cause cognitive impairment -History of psychiatric disorders such as major depression or personality disorders\n* Alcohol and drug addiction","ALL","18 Years","75 Years",{"count":83,"type":84},45,"ESTIMATED","INTERVENTIONAL",[87],"NA","The primary aim of this study is to compare the efficacy of Transcutaneous Electrical Nerve Stimulation (TENS) and Low Level Laser Therapy (LLLT), which are analgesic modalities that play an important role in the treatment of this frequently encountered complication. The secondary aim of the study is to evaluate its effectiveness on upper extremity function, quality of life, sleep, and fatigue.",[90],"Hemiplegic Shoulder Pain",[92,28,33,93,94,95],"Hemiplegic shoulder pain","Ultrasonographic evaluation","Upper extremity function","stroke","2026-06-16",{"date":98,"type":99},"2026-06-17","ACTUAL",{"date":101,"type":99},"2025-09-24",{"date":103,"type":84},"2026-08-31",{"name":5,"class":6},1]