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NOT YET RECRUITING
NCT07227662
NA

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

Sponsor: University of Maryland, Baltimore

View on ClinicalTrials.gov

Summary

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.

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

10

Start Date

2026-03-01

Completion Date

2026-12-01

Last Updated

2026-02-13

Healthy Volunteers

No

Interventions

DEVICE

Home based FES in combination with usual therapy

Participants diagnosed with shoulder adhesive capsulitis and being treated at a local physical and occupational therapy outpatient clinic will be deemed eligible for inclusion in the study.The intervention will include home use of Genesis Flex FES device alongside usual rehabilitation care. Usual care therapy may consist of manual therapy, hot packs, transcutaneous electrical nerve stimulation, ultrasound treatments, daily home-based shoulder exercises, and/or acetaminophen for pain, which will be documented.

Locations (1)

University of Maryland School of Medicine, Baltimore, Maryland

Baltimore, Maryland, United States