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Feasibility, Usability and Preliminary Efficacy of Home-based FES Fro Adhesive Capsulitis

StatusRecruiting
PhaseNot applicable
Started
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Record History

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  1. Recruitment opened Show 4 more changesShow less
    • Eligibility criteria expanded, about 11 words
    • Secondary endpoints: details revised at 2 of 3 entries
    • Site details revised
    • Publications: details revised at 10 of 11 entries
  2. Start date: Mar 1, 2026 to Jun 1, 2026v4
  3. Start date: Dec 1, 2025 to Mar 1, 2026v3
  4. Secondary endpoints: details revised at 1 of 3 entriesv2
  5. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The purpose of this study is to investigate the feasibility, usability and preliminary efficacy of a home-based Functional Electrical Stimulation(FES) in individuals with shoulder adhesive capsulitis. The main question it aims to answer is if combining home-based FES to usual therapy at the clinic will improve pain and improve function of the impaired shoulder.
Trial Details
NCT Number NCT07227662
Lead Sponsor University of Maryland, Baltimore
Conditions
(from sponsor)		 Shoulder Adhesive Capsulitis
Related terms Bursitis
Enrollment 10 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov