By InvitationNot Applicable

Shoulder Pacemaker for Scapular Dyskinesia

United States20 participantsStarted 2021-09-27

Plain-language 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.

Who can participate

Age range18 Years – 80 Years

SexALL

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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.

What they're measuring

Visual Analog Scale (VAS) pain

Timeframe: Beginning of the study prior to initiating use of the pacemaker

Visual Analog Scale (VAS) pain

Timeframe: 3-months

Visual Analog Scale (VAS) pain

Timeframe: 6-months

Visual Analog Scale (VAS) pain

Timeframe: 12-months

Trial details

NCT IDNCT05116722

SponsorUniversity of Utah

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2028-09

View on ClinicalTrials.gov More Scapular Dyskinesis trials