Actively Recruiting
Static vs. Dynamic Progressive Splinting for Persistent Wrist Stiffness After DRF
Led by Al Hayah University In Cairo · Updated on 2025-04-06
50
Participants Needed
1
Research Sites
52 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This randomized controlled trial will compare the effectiveness of static progressive splinting versus dynamic splinting for treating persistent wrist stiffness in adults ≥18 years old at least 8 weeks post distal radius fracture (DRF) injury. Both splinting modalities are provided as an adjunct to one weekly supervised therapy session over a 6-week period. The primary outcomes are wrist active and passive range of motion (AROM/PROM) measured using goniometry, with secondary outcomes including patient-reported wrist function (PRWE), overall satisfaction, and adverse events.
CONDITIONS
Official Title
Static vs. Dynamic Progressive Splinting for Persistent Wrist Stiffness After DRF
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults aged 18 years or older
- At least 8 weeks post distal radius fracture (operative or nonoperative) with completed standard rehabilitation
- Persistent wrist stiffness with 50% or less of contralateral wrist extension or flexion
- Able to provide written informed consent and follow study procedures
You will not qualify if you...
- Complex regional pain syndrome (CRPS) or active fracture healing problems
- Significant wrist problems unrelated to the distal radius fracture
- Uncontrolled medical conditions interfering with splint use or therapy
- Skin conditions or allergies preventing orthosis use
- Inability or unwillingness to follow the treatment or follow-up schedule
- Pregnant or breastfeeding individuals
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Faculty of Physical Therapy, Al Hayah University
Cairo, Egypt, 12311
Actively Recruiting
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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