Shoulder Pacemaker for Scapular Dyskinesia

Enrolling by invitation · Not applicable

Conditions studied: Scapular Dyskinesis, Posterior Shoulder Instability

In brief

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 facts

Study ID

NCT05116722

Run by

University of Utah

People needed

20

Starts

2021-09-27

Expected to finish

2028-09-01

Last updated by the study team

2026-05-05

Who can join

Age: 18 and older, up to 80. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Scapular Dyskinesis
• Posterior Shoulder Instability

You may not qualify if…

• Rotator Cuff Tearing
• Shoulder Arthritis
• Patients with implantable electrical/electronic devices
• If participants are using wearable electrical medical devices, such as glucose sensors or infusion pumps, these devices will be turned off or the participants will be excluded from the study.

Where it is running

• University Of Utah Orthopedics Center — Salt Lake City, Utah, United States

Full record on ClinicalTrials.gov

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