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 — BEHAVIORAL
    The 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: Control
    The control arm will receive the standard of care treatment for ulnar sided wrist pain
  • Experimental: Blood Flow Restriction
    The 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)

FacilityCityStateZIPSite coordinators
Stanford UniversityRedwood CityCalifornia94063-

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