[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Celal Bayar University\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":133},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,45,76,105],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":27,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":33,"lastUpdatePostDateStruct":34,"startDateStruct":37,"completionDateStruct":39,"leadSponsor":41,"locationsCount":44},"100641044","the-effect-of-auditory-stimulation-and-the-love-glove-technique-100641044",false,"NCT07602998","The Effect of Auditory Stimulation and the \"Love Glove\" Technique","The Effect of Auditory Stimulation and the \"Love Glove\" Technique on Vital Signs in Unconscious Patients","Inclusion Criteria:\n\n* Patients in a coma who have been hospitalized in the intensive care unit for at least 48 hours, have a Glasgow Coma Scale score of 8 or lower,\n* have no hearing problems,\n* are hemodynamically stable,\n* are either on mechanical ventilation or breathing spontaneously, have no history of head trauma,\n* have received informed consent from their legal representative\n\nExclusion Criteria:\n\n* Patients with open wounds,\n* those diagnosed with brain death,\n* those whose sedative or analgesic doses were adjusted during the study,\n* those with severe hemodynamic instability,\n* patients with latex allergies","ALL","18 Years",{"count":19,"type":20},100,"ESTIMATED","INTERVENTIONAL",[23],"NA","The aim of this study was to determine the effect of the \"love glove\" intervention, combined with the voices of family members and nurses, on vital signs in unconscious patients in the intensive care unit. The following items will be used to collect research data: Patient Information Form (Appendix I), Data Recording Form (Appendix II), MP3 player, external headphones and voice recorder, latex gloves, and thermometer.\n\nData Collection Tools:\n\nPatient Identification Form : A form containing patients' sociodemographic characteristics and their Glasgow Coma Scale score prior to the start of the study Data Recording Form: A form used to record patients' level of consciousness and hemodynamic parameters before and after the auditory stimulation procedure.\n\nMethods This study is a randomized controlled trial designed to determine the effect of applying a family member's voice, a nurse's voice, and the \"love glove\" on vital signs in unconscious patients admitted to the intensive care unit. Following approval from the ethics committee, the study is planned to be conducted with comatose patients admitted to the hospital's intensive care unit.",[26],"Unconscious State",[28,29,30,31],"Auditory Stimulation","Love Glove","Vital Signs","Tactile Stimulation","NOT_YET_RECRUITING","2026-05-16",{"date":35,"type":36},"2026-05-22","ACTUAL",{"date":38,"type":20},"2026-06",{"date":40,"type":20},"2028-04",{"name":42,"class":43},"Celal Bayar University","OTHER",1,{"id":46,"slug":47,"hasResults":11,"nctId":48,"briefTitle":49,"officialTitle":50,"acronym":4,"eligibilityCriteria":51,"healthyVolunteers":11,"sex":52,"minAge":17,"maxAge":53,"enrollmentInfo":54,"targetDuration":4,"studyType":21,"phases":56,"briefSummary":57,"conditions":58,"keywords":60,"overallStatus":67,"whyStopped":4,"lastUpdateSubmitDate":68,"lastUpdatePostDateStruct":69,"startDateStruct":71,"completionDateStruct":73,"leadSponsor":75,"locationsCount":44},"100591146","effect-of-helfer-skin-tap-and-cold-application-on-pain-and-hemodynamics-during-vaccination-100591146","NCT06976632","Effect of Helfer Skin Tap and Cold Application on Pain and Hemodynamics During Vaccination","Comparison of the Effects of the Helfer Skin Tap Technique and Local Cold Application on Pain and Hemodynamic Parameters During Vaccination in Pregnant Women","Inclusion Criteria: Pregnant women who meet the following criteria will be included in the study:\n\n* Over the age of 18,\n* Scheduled to receive a tetanus vaccine,\n* Able to speak and communicate in Turkish,\n* Willing to participate in the study,\n* Not experiencing any pain for any reason prior to the injection.\n\nExclusion Criteria: Pregnant women who meet any of the following criteria will be excluded from the study:\n\n* Under the age of 18,\n* Received a tetanus vaccine for reasons other than pregnancy,\n* Received a vaccine other than tetanus,\n* Experiencing pain for any reason prior to the vaccine,\n* Have circulatory disorders or peripheral vascular disease,\n* Have bleeding or clotting disorders,\n* Have a local infection,\n* Used painkillers at least 6 hours prior to the procedure,\n* Underwent a painful procedure within the last hour,\n* Have cold sensitivity,\n* Have cognitive or psychological issues.","FEMALE","42 Years",{"count":55,"type":20},90,[23],"The purpose of this study is to investigate the effect of local cold application using the Helfer Skin Tap Technique on pain levels during the intramuscular injection of the tetanus vaccine in pregnant women. The study will also record vital signs, which are among the physiological effects of pain.",[59],"Pregnant Women",[61,62,63,64,65,66],"immunization","pain","hemodynamic parameters","pregnant women","local cold application","helfer skin tap tecnique","RECRUITING","2026-03-18",{"date":70,"type":36},"2026-03-20",{"date":72,"type":36},"2025-05-09",{"date":74,"type":20},"2026-06-09",{"name":42,"class":43},{"id":77,"slug":78,"hasResults":11,"nctId":79,"briefTitle":80,"officialTitle":81,"acronym":4,"eligibilityCriteria":82,"healthyVolunteers":11,"sex":16,"minAge":83,"maxAge":84,"enrollmentInfo":85,"targetDuration":4,"studyType":21,"phases":87,"briefSummary":88,"conditions":89,"keywords":91,"overallStatus":67,"whyStopped":4,"lastUpdateSubmitDate":97,"lastUpdatePostDateStruct":98,"startDateStruct":100,"completionDateStruct":102,"leadSponsor":104,"locationsCount":44},"100619411","the-effects-of-proprioceptive-neuromuscular-facilitation-100619411","NCT07344272","The Effects of Proprioceptive Neuromuscular Facilitation","The Effects of Proprioceptive Neuromuscular Facilitation on Shoulder Girdle Function and Quality of Life in Individuals With Scapular Winging","Inclusion Criteria:\n\n* Volunteering to participate in the study.\n* Presenting with bilateral scapular winging (Scapular winging will be evaluated by measuring the distance between the inferior angle of the scapula and the thoracic wall using a scapulometer; a distance of ≥2 cm is considered as winging).\n\nExclusion Criteria:\n\n* Presence of long thoracic nerve palsy.\n* Having undergone shoulder surgery within the last 12 months or having an acute shoulder injury (e.g., rotator cuff tear, dislocation, labral pathology, etc.).\n* Presence of scapulothoracic bursitis, fractures, tumors, or structural deformities in the scapular\u002Fthoracic region.\n* Having received regular scapular or shoulder rehabilitation within the last 6 months.","20 Years","40 Years",{"count":86,"type":20},50,[23],"This study aims to investigate the effects of proprioceptive neuromuscular facilitation (PNF) on shoulder girdle function and quality of life in individuals with scapular winging.",[90],"Scapular Winging",[92,93,94,95,96],"Functional status","Neuromuscular effect","Proprioceptive neuromuscular facilitation","Quality of life","Scapula","2026-03-12",{"date":99,"type":36},"2026-03-13",{"date":101,"type":36},"2026-02-01",{"date":103,"type":20},"2026-03-15",{"name":42,"class":43},{"id":106,"slug":107,"hasResults":11,"nctId":108,"briefTitle":109,"officialTitle":110,"acronym":4,"eligibilityCriteria":111,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":112,"targetDuration":4,"studyType":21,"phases":114,"briefSummary":115,"conditions":116,"keywords":118,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":125,"lastUpdatePostDateStruct":126,"startDateStruct":128,"completionDateStruct":130,"leadSponsor":132,"locationsCount":4},"100606593","virtual-reality-during-passive-motion-after-knee-surgery-100606593","NCT07177573","Virtual Reality During Passive Motion After Knee Surgery","The Effects of Virtual Reality on Pain, Anxiety, and Comfort During Continuous Passive Motion After Total Knee Arthroplasty","Inclusion Criteria:\n\nFirst-time total knee arthroplasty Postoperative day 2 Mobilized before CPM application Adequate vision and hearing to use the virtual reality device Oriented to person, place, and time No cognitive, sensory, or verbal communication impairments No history of vertigo No hypertension Not using sedative, anxiolytic, or similar medications Willing to voluntarily participate in the study\n\nExclusion Criteria:\n\n* Any diagnosed psychiatric disorder\n* History of vertigo\n* Hypertension\n* Using sedative, anxiolytic, or similar medications\n* Poor general condition\n* Unwillingness to participate",{"count":113,"type":20},102,[23],"The purpose of this study is to investigate the effects of virtual reality on pain, anxiety, and comfort during continuous passive motion following total knee arthroplasty",[117],"Total Knee Arthroplasty",[117,119,120,121,122,123,124],"Virtual Reality","Continuous Passive Movement Therapy","Pain","Anxiety","Comfort","Patient","2025-09-17",{"date":127,"type":36},"2025-09-22",{"date":129,"type":20},"2025-09",{"date":131,"type":20},"2026-10-01",{"name":42,"class":43},""]