Feasibility, Usability and Preliminary Efficacy of Home-based FES Fro Adhesive Capsulitis
- Shoulder Adhesive Capsulitis
At a glance
- Phase
- Phase not stated
- Study type
- Interventional
- Sponsor
- University of Maryland, Baltimore
- Enrolment target
- 10
- Started
- 1 June 2026
- Main results due
- 1 December 2026
- Study sites
- 1
- Registry updated
- 25 September 2026
Can you take part?
- Aged 18 years and over.
- Open to any sex.
- You need the condition being studied — healthy volunteers are not accepted.
These are the headline rules only. Every study has a longer list, and whether you are eligible is decided by the research team at the site — never by this page.
Read the full eligibility criteria
Inclusion Criteria: 1. Age \> 18 years 2. Individuals diagnosed with shoulder adhesive capsulitis 3. Shoulder pain, limited shoulder mobility for more than 4 weeks, normal shoulder x-ray findings, and normal neurological exam 4. Can tolerate electrical stimulation Exclusion Criteria: 1. Presence of shoulder tumors or bone lesions 2. History of shoulder fracture or subluxation 3. History of shoulder surgery 4. Severe osteoporosis, 5. Rheumatic disease 6. Radiating pain from cervical radiculopathy 7. Participation in other clinical trial, and/or intraarticular steroid injections within 6 weeks
What this study is about
In the sponsor’s own words, from the registry.
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.
Study sites(1)
University of Maryland School of Medicine, Baltimore, Maryland
Baltimore, Maryland, United States
Recruiting
Showing 1 of 1 sites. 1 of the 1 site on this study is recruiting right now — a site can stop enrolling while the study as a whole is still open.
Source: ClinicalTrials.gov record NCT07227662. Trialion does not run this study, is not paid to refer anyone to it, and cannot enrol you. Eligibility is always decided by the research team at the site.
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