[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100648478":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":26,"centralContacts":26,"locations":26,"responsibleParty":31,"collaborators":26,"id":36,"slug":37,"hasResults":38,"nctId":39,"briefTitle":40,"officialTitle":41,"acronym":42,"eligibilityCriteria":43,"healthyVolunteers":38,"sex":44,"minAge":45,"maxAge":46,"enrollmentInfo":47,"targetDuration":26,"studyType":50,"phases":51,"briefSummary":53,"conditions":54,"keywords":56,"overallStatus":63,"whyStopped":26,"lastUpdateSubmitDate":64,"lastUpdatePostDateStruct":65,"startDateStruct":68,"completionDateStruct":70,"leadSponsor":72,"locationsCount":26},{"fullName":5,"class":6},"Istanbul University","OTHER",[8,15],{"label":9,"type":10,"description":11,"interventionNames":12},"Whole-Body Vibration + Conventional Rehabilitation","EXPERIMENTAL","Participants assigned to this arm will receive conventional rehabilitation combined with whole-body vibration therapy three times per week for 8 weeks.",[13,14],"Device: Whole-Body Vibration Therapy","Other: Conventional Rehabilitation Exercise Program",{"label":16,"type":17,"description":18,"interventionNames":19},"Conventional Rehabilitation","ACTIVE_COMPARATOR","Participants assigned to this arm will receive the same conventional rehabilitation program without whole-body vibration therapy for 8 weeks.",[14],[21,27],{"type":22,"name":23,"description":24,"armGroupLabels":25,"otherNames":26},"DEVICE","Whole-Body Vibration Therapy","Whole-body vibration therapy will be administered using a Power Plate device at a frequency of 35 Hz and an amplitude of 2 mm, three sessions per week for 8 weeks, in addition to a standardized conventional rehabilitation program.",[9],null,{"type":6,"name":28,"description":29,"armGroupLabels":30,"otherNames":26},"Conventional Rehabilitation Exercise Program","Participants will receive a standardized conventional rehabilitation program including range of motion exercises, strengthening exercises, proprioceptive training, functional activities, and patient education three times per week for 8 weeks.",[16,9],{"type":32,"investigatorFullName":33,"investigatorTitle":34,"investigatorAffiliation":35,"oldNameTitle":26,"oldOrganization":26},"PRINCIPAL_INVESTIGATOR","Tugba Civi Karaaslan","Assistant Professor","Istanbul University - Cerrahpasa","100648478","effect-of-whole-body-vibration-on-rehabilitation-in-distal-radius-fractures-100648478",false,"NCT07723456","Effect of Whole Body Vibration on Rehabilitation in Distal Radius Fractures","Effect Of Whole Body Vibration On Functional And Sensorimotor Recovery In Conservatively Treated Distal Radius Fractures: A Randomized Controlled Trial","WBV-DRF","Inclusion Criteria:\n\n* Adults aged 18 to 65 years.\n* Unilateral distal radius fracture treated conservatively with cast or splint.\n* Completion of the immobilization period with radiologically confirmed stable callus formation.\n* Referred for physiotherapy after conservative treatment.\n* Able to understand study procedures and provide written informed consent.\n* Initiation of rehabilitation within 72 hours after cast removal.\n\nExclusion Criteria:\n\n* Previous surgery or severe trauma to the affected upper extremity.\n* Open wound or active infection at the fracture site.\n* Peripheral neuropathy or severe neurological disorders.\n* Vestibular disorders or conditions contraindicating whole-body vibration therapy.\n* Pregnancy.\n* Severe osteoporosis.\n* Active inflammatory or vascular disease affecting the upper extremity.\n* Cognitive impairment preventing participation in the study.\n* Inability to attend the rehabilitation program regularly.","ALL","18 Years","65 Years",{"count":48,"type":49},66,"ESTIMATED","INTERVENTIONAL",[52],"NA","This study is a randomized controlled clinical trial designed to evaluate the effects of whole body vibration (WBV) added to conventional rehabilitation on functional and sensorimotor recovery in patients with conservatively treated distal radius fractures. Following immobilization, patients often experience pain, reduced range of motion, decreased muscle strength, and impaired proprioception, which negatively affect functional recovery. WBV is thought to enhance neuromuscular activation and improve proprioceptive input, thereby contributing to functional performance.\n\nParticipants will be randomly assigned into two groups; the experimental group will receive WBV in addition to conventional rehabilitation three times per week for eight weeks, while the control group will receive only conventional rehabilitation. Assessments will be conducted at baseline, week 4, and week 8. The primary outcome measure is the Patient-Rated Wrist Evaluation (PRWE), while secondary outcomes include QuickDASH, Numeric Pain Rating Scale (NPRS), joint position sense, grip strength, range of motion, and fine motor skills.",[55],"Distal Radius Fracture",[55,57,58,59,60,61,62],"Whole Body Vibration","Proprioception","Sensorimotor Function","Wrist Rehabilitation","Randomized Controlled Trial","Conservative Treatment","NOT_YET_RECRUITING","2026-07-22",{"date":66,"type":67},"2026-07-23","ACTUAL",{"date":69,"type":49},"2026-07-25",{"date":71,"type":49},"2027-05-25",{"name":5,"class":6}]