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NCT06251206 · ClinicalTrials.gov registry record · Phase 1
Impact of Early ADL Education on Outcomes Post DRF ORIF
A Phase 1 study of Distal Radius Fractures, sponsored by George Washington University.
- Recruiting
- Registry status
- Phase 1
- Development phase
- 64
- Enrollment target
- 1
- Study location
NCT06251206: Recruiting Phase 1 study of Distal Radius Fractures, sponsored by George Washington University.
NCT06251206 is a Phase 1 study of Distal Radius Fractures that is actively recruiting participants, run by George Washington University. The registered enrollment target is 64 participants, below the 180-participant average among 4 other Distal Radius Fractures trials with a reported enrollment target (64% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT06251206, a Phase 1 study of Distal Radius Fractures, is actively recruiting participants, sponsored by George Washington University.
- RECRUITING
- Registry status
- Phase 1
- Development phase
- 64 participants
- Enrollment target
- 1
- Study location
Study Summary
This study is a randomized controlled trial (RCT). This RCT which will study the effect of performing daily activities early after a distal radius fracture being treated with surgical intervention of open reduction and internal fixation. This study will have two groups. The experimental group will watch a video and be given a handout on how to perform daily activities with the hand of the injured wrist while recovering from surgery and postoperative instructions. The control group will watch a video on wound care and be given a handout on postoperative instructions. Outcome measures will be taken at initial evaluation between 1-2 weeks post surgery, at 5-7 weeks post surgery, at 8-10 weeks, and at 12-14 weeks. Outcome measures will include the Michigan Wrist Evaluation, Visual Analog Pain Scale, Tampa Scale of Kinesiophobia-11 Scale, finger mobility testing, grip and pinch strength, and the 9 hole peg test to test fine motor coordination. Outcome measure scores will be compared between groups using a t-test statistical test. Outcome measure scores will also be tested within groups using a paired t-test.
Primary Outcome
Patient reported outcome measure for function
Conditions Studied
Interventions
- BEHAVIORAL ADL/Postoperative Instruction
- BEHAVIORAL Postoperative Instruction
Study Locations (1)
Virginia
- Medical Facilities Associates - Washington
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 64 participants |
| Start Date | 2024-08-01 |
| Est. Completion | 2026-09 |
| Phase | Phase 1 |
What NCT06251206 shows while recruiting
NCT06251206 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 64 participants, a relatively small participant target, below the 180-participant average among 4 other Distal Radius Fractures trials with a reported enrollment target (64% lower).
The record links to 1 condition, with Distal Radius Fractures appearing as the primary indexed condition, and to 2 interventions - of which ADL/Postoperative Instruction is the first listed.
NCT06251206 reports a single indexed study location in Virginia.
Frequently Asked Questions
What is clinical trial NCT06251206 about?
NCT06251206 is a clinical study titled "Impact of Early ADL Education on Outcomes Post DRF ORIF". This study is a randomized controlled trial (RCT). This RCT which will study the effect of performing daily activities early after a distal radius fracture being treated with surgical intervention of open reduction and internal fixation. This study will have two groups. The experimental group will w...
What is the current status of trial NCT06251206?
This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 64 participants. The study started on 2024-08-01. Estimated completion is 2026-09.
What conditions does trial NCT06251206 study?
This clinical trial studies the following conditions: Distal Radius Fractures.
What interventions are being tested in trial NCT06251206?
The interventions under investigation include: ADL/Postoperative Instruction (BEHAVIORAL), Postoperative Instruction (BEHAVIORAL).
Who is sponsoring clinical trial NCT06251206?
This trial is sponsored by George Washington University, which has 133 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06251206 being conducted?
This trial has 1 study location across Virginia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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