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Recruiting NCT07227662

NCT07227662 Feasibility, Usability and Preliminary Efficacy of Home-based FES Fro Adhesive Capsulitis

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Clinical Trial Summary
NCT ID NCT07227662
Status Recruiting
Phase —
Sponsor University of Maryland, Baltimore
Condition Shoulder Adhesive Capsulitis
Study Type INTERVENTIONAL
Enrollment 10 participants
Start Date 2026-06-01
Primary Completion 2026-12-01

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
Home based FES in combination with usual therapy

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 10 participants in total. It began in 2026-06-01 with a primary completion date of 2026-12-01.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief 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.

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

Contact & Investigator

Central Contact

Sanjana Rao, PhD

✉ sanjana.rao@som.umaryland.edu

📞 4438256349

Frequently Asked Questions

Who can join the NCT07227662 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Shoulder Adhesive Capsulitis. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07227662 currently recruiting?

Yes, NCT07227662 is actively recruiting participants. Contact the research team at sanjana.rao@som.umaryland.edu for enrollment information.

Where is the NCT07227662 trial being conducted?

This trial is being conducted at Baltimore, United States.

Who is sponsoring the NCT07227662 clinical trial?

NCT07227662 is sponsored by University of Maryland, Baltimore. The trial plans to enroll 10 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: November 2026  ·  Data Methodology