Skip to content

Shoulder Pacemaker for Scapular Dyskinesia

Shoulder Pacemaker for the Treatment of Scapular Dyskinesia

Status
Enrolling by invitation
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05116722
Enrollment
20
Registered
2021-11-11
Start date
2021-09-27
Completion date
2028-09-01
Last updated
2026-05-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Posterior Shoulder Instability, Scapular Dyskinesis

Keywords

Scapular Dyskinesia, Posterior Shoulder Instability, Shoulder Pacemaker, Treatment, Pain

Brief summary

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.

Detailed description

The scapula plays a key role in nearly every aspect of normal shoulder function. Shoulder dyskinesia or scapula winging effects patients as a result of nerve injury or muscle detachment or abnormal muscle recruitment. Patients with abnormal muscle recruitment often are helped the most by therapy but restoring normal firing can be difficult. Abnormal muscle recruitment is due to pain or weakness or instability of the glenohumeral joint and the muscles around the scapula attempt to compensate for the lack of normal firing patterns. In many patients, physical therapy and surgery have proven to be unsuccessful treatment options. The Shoulder Pacemaker is a device that specifically aims at resolving functional issues that surgery and physical therapy are unable. It's a wearable electro stimulator created for patients suffering from unbalanced muscle activation in the shoulder, such as Scapular Dyskinesis. The Shoulder Pacemaker delivers "smart stimulation" through a dynamic interaction between the patient and the device. The motion technology recognizes muscle movement and automatically sets the appropriate stimulation intensity according to the movement. This process helps to restore normal muscle activation patterns and equilibrium. The pacemaker will hopefully assist in restoring normal muscle recruitment.

Interventions

DEVICEShoulder Pacemaker

Shoulder pacemaker treatment for 15 - 30 minutes at 3-months, 6-months and 12-months during physical therapy.

Sponsors

University of Utah
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Scapular Dyskinesis * Posterior Shoulder Instability

Exclusion criteria

* 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.

Design outcomes

Primary

MeasureTime frameDescription
Visual Analog Scale (VAS) painBeginning of the study prior to initiating use of the pacemakerVAS pain score (0 no pain - 10 severe pain)

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORRobert Z Tashjian, MD

University of Utah Orthopaedics

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 6, 2026