Impact of early education on daily activities after wrist surgery
Impact of Early Multimodal ADL Education on Outcomes Post Distal Radius Fracture Open Reduction Internal Fixation Surgery
This study tests if giving patients early education on daily activities after wrist surgery helps them recover better than just standard care instructions.
Quick facts
| Phase | Phase 1 |
|---|---|
| Study type | Interventional |
| Enrollment | 64 (estimated) |
| Ages | 18 Years to 110 Years |
| Sex | All |
| Sponsor | George Washington University Academic / other |
| Locations | 1 site (Washington, Virginia) |
| Trial ID | NCT06251206 on ClinicalTrials.gov |
What this trial studies
This randomized controlled trial investigates the effects of early education on activities of daily living (ADL) for patients recovering from distal radius fractures treated with open reduction and internal fixation. Participants will be divided into two groups: one receiving educational materials on performing daily activities with the injured wrist, and the other receiving standard postoperative care instructions. Outcome measures will be assessed at multiple time points post-surgery to evaluate recovery progress, including pain levels, mobility, and strength. The study aims to determine if early ADL education can enhance recovery outcomes compared to standard care.
Who should consider this trial
Good fit: Ideal candidates are English-speaking adults aged 18 and older who are within two weeks post-surgery for a distal radius fracture.
Not a fit: Patients with pre-existing neurological conditions, cognitive or psychological deficits, or multiple injuries to the upper limb may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could lead to improved recovery outcomes and enhanced quality of life for patients after wrist surgery.
How similar studies have performed: While similar educational interventions have shown promise in other surgical recovery contexts, this specific approach is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: English Speaking DRF treated with ORIF Individuals 18 years of age or older 2 weeks or less post ORIF for DRF Exclusion Criteria: Individuals with pre-existing neurological coniditons affecting the upper limb Individuals with congnitive deficits that would limit the ability to correctly report information on outcome measures Individuals with psychological deficits which would limit the ability to correctly report information on outcome measures Individuals with multiple injuries to the affected upper limb Individuals with multiple injuries to both upper limbs Prior distal radius fracture involving the same wrist Individuals receiving hand therapy for another injury at enrollment into study
Where this trial is running
Washington, Virginia
- Medical Facilities Associates — Washington, Virginia, United States (Recruiting)
Study contacts
- Study coordinator: Sarah Doerrer, PhD
- Email: sdoerrer56@gwu.edu
- Phone: 757-651-5110
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.