Effect of Whole Body Vibration on Rehabilitation in Distal Radius Fractures (NCT07723456) | Clinical Trial Compass
Not Yet RecruitingNot Applicable
Effect of Whole Body Vibration on Rehabilitation in Distal Radius Fractures
66 participantsStarted 2026-07-25
Plain-language summary
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.
Participants 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.
Who can participate
Age range
18 Years – 65 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Adults aged 18 to 65 years.
* Unilateral distal radius fracture treated conservatively with cast or splint.
* Completion of the immobilization period with radiologically confirmed stable callus formation.
* Referred for physiotherapy after conservative treatment.
* Able to understand study procedures and provide written informed consent.
* Initiation of rehabilitation within 72 hours after cast removal.
Exclusion Criteria:
* Previous surgery or severe trauma to the affected upper extremity.
* Open wound or active infection at the fracture site.
* Peripheral neuropathy or severe neurological disorders.
* Vestibular disorders or conditions contraindicating whole-body vibration therapy.
* Pregnancy.
* Severe osteoporosis.
* Active inflammatory or vascular disease affecting the upper extremity.
* Cognitive impairment preventing participation in the study.
* Inability to attend the rehabilitation program regularly.
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Patient-Rated Wrist Evaluation (PRWE) Score
Timeframe: From baseline to Week 8 (assessed at baseline, Week 4, and Week 8)