Blood Flow Restriction for Ulnar Sided Wrist Pain
Part of paid clinical trials in Redwood City, California.
- Sponsor
- Stanford University
- Study ID
- NCT06963671
- Status
- Enrolling By Invitation
Conditions
- Ulnar Wrist Pain
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Blood Flow Restriction — BEHAVIORALThe treatment group will receive standard rehabilitation as a home program plus low-load resistance training with BFR application while at the hand therapy clinic for their appointments
Study Details
The purpose of this study is to determine the strength, pain and functional benefits of early, low-load resistance training with blood flow restriction (BFR) in ulnar-sided wrist pain treated nonoperatively with immobilization for 4-6 weeks. Hypothesis: patients in the BFR group with have improved grip strength and patient reported outcome measure scores compared to the control group.
Key Dates
- Start date
- Aug 11, 2025
- Status verified
- Sep 2025
- Primary completion
- Dec 31, 2028
- Completion
- Dec 31, 2028
Study Design
- Enrollment
- 90 participants (estimated)
- Allocation
- NON_RANDOMIZED
- Intervention model
- SEQUENTIAL
- Primary purpose
- TREATMENT
Arms
- No Intervention: ControlThe control arm will receive the standard of care treatment for ulnar sided wrist pain
- Experimental: Blood Flow RestrictionThe Blood Flow Restriction group will receive BFR treatment
Primary Outcome Measure
Grip Strength [ Time Frame: From enrollment to 6 weeks after initiation of BRF ]
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Stanford University | Redwood City | California | 94063 | - |
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