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 — DEVICE
    Shoulder 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 Treatment
    The 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)

FacilityCityStateZIPSite coordinators
University Of Utah Orthopedics CenterSalt Lake CityUtah84108-

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