Clinical trial Recruiting at 1 site Phase 1 Interventional Ages 18 to 110

Impact of early education on daily activities after wrist surgery

Official title: Impact of Early Multimodal ADL Education on Outcomes Post Distal Radius Fracture Open Reduction Internal Fixation Surgery

Run by George Washington University · NCT06251206 · Data updated 2026-11-12

This study tests if giving patients early education on daily activities after wrist surgery helps them recover better than just standard care instructions.

More Distal Radius Fractures trials

Quick facts

PhasePhase 1
Study typeInterventional
Ages18 Years to 110 Years
SexAll
Enrollment64 (estimated)
SponsorGeorge Washington University
Academic / other
Locations1 site (Washington, Virginia)
StatusRecruiting
StartedAugust 1, 2024
Main results expectedAugust 2027
Study endsDecember 2027
Registry record updatedOctober 19, 2026
Trial IDNCT06251206 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are English-speaking adults aged 18 and older who are within two weeks post-surgery for a distal radius fracture.

Probably 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.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

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.

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 gone: While similar educational interventions have shown promise in other surgical recovery contexts, this specific approach is relatively novel.

Who can join: the full rules

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 it's running

  • Medical Facilities Associates
    Washington, Virginia, United States
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.