Shoulder Pacemaker for Scapular Dyskinesia
Part of paid clinical trials in Salt Lake City, Utah.
- Sponsor
- University of Utah
- Study ID
- NCT05116722
- Status
- Enrolling By Invitation
Conditions
- Posterior Shoulder Instability
- Scapular Dyskinesis
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 80 Years
- Healthy Volunteers
- Not accepted
Interventions
- Shoulder Pacemaker — DEVICEShoulder pacemaker treatment for 15 - 30 minutes at 3-months, 6-months and 12-months during physical therapy.
Study Details
The investigators purpose of this study is to determine patients-reported outcomes (VAS pain scores) in patients with Scapular Dyskinesis or Posterior Shoulder Instability who undergo rehabilitation with a shoulder pacemaker.
Key Dates
- Start date
- Sep 27, 2021
- Status verified
- Apr 2026
- Primary completion
- Sep 30, 2028
- Completion
- Sep 30, 2028
Study Design
- Enrollment
- 20 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Shoulder Pacemaker TreatmentThe patients will be treated using the pacemaker for 15 - 30 minutes at 3-months, 6-months and 12-months during physical therapy.
Primary Outcome Measure
Visual Analog Scale (VAS) pain [ Time Frame: Beginning of the study prior to initiating use of the pacemaker ]
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| University Of Utah Orthopedics Center | Salt Lake City | Utah | 84108 | - |
Find similar trials in Salt Lake City, UT
By research site