Comparing two types of splints for wrist stiffness after a fracture
A Two-Arm, Parallel-Group Randomized Controlled Trial Comparing Static Progressive Splinting Versus Dynamic Splinting for Improving Wrist PROM/AROM in Patients With Persistent Post-DRF Stiffness
NA · Al Hayah University In Cairo · NCT06913933
This study is testing which type of splint, static progressive or dynamic, helps adults with wrist stiffness after a fracture feel better and move their wrist more easily.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 50 (estimated) |
| Ages | 18 Years to 65 Years |
| Sex | All |
| Sponsor | Al Hayah University In Cairo (other) |
| Locations | 1 site (Cairo) |
| Trial ID | NCT06913933 on ClinicalTrials.gov |
What this trial studies
This clinical trial compares the effectiveness of static progressive splinting and dynamic splinting in treating persistent wrist stiffness in adults who are at least 8 weeks post distal radius fracture. Participants will receive one weekly supervised therapy session alongside their assigned splinting method over a 6-week period. The study aims to measure improvements in wrist range of motion and patient-reported outcomes, including satisfaction and function. Both splinting techniques will be evaluated to determine which is more effective in alleviating stiffness.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18 years or older who have persistent wrist stiffness following a distal radius fracture and have completed standard rehabilitation.
Not a fit: Patients with complex regional pain syndrome, significant wrist pathology unrelated to the fracture, or uncontrolled medical conditions may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide patients with a more effective treatment option for improving wrist mobility and function after a distal radius fracture.
How similar studies have performed: While there is limited information on the success of similar studies, the comparison of splinting techniques for wrist stiffness is a relevant area of investigation that may yield valuable insights.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: Adults aged 18 years or older. At least 8 weeks post distal radius fracture (operative or nonoperative) who have completed standard rehabilitation. Demonstrated persistent wrist stiffness with ≤50% of contralateral wrist extension or flexion. Capable of providing written informed consent and complying with study procedures Exclusion Criteria: Presence of complex regional pain syndrome (CRPS) or active fracture healing issues. History of significant wrist pathology unrelated to the DRF. Uncontrolled medical conditions that would interfere with splint application or therapy. Known skin conditions or allergies that preclude orthosis use. Inability or unwillingness to adhere to the intervention protocol or follow-up schedule. Pregnant or breastfeeding individuals.
Where this trial is running
Cairo
- Faculty of Physical Therapy, Al Hayah University — Cairo, Egypt (RECRUITING)
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Distal Radius Fractures