Feasibility, Usability and Preliminary Efficacy of Home-based FES Fro Adhesive Capsulitis
NCT: NCT07227662 · NOT_YET_RECRUITING
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.
Frequently Asked Questions
What is Feasibility, Usability and Preliminary Efficacy of Home-based FES Fro Adhesive Capsulitis?
Feasibility, Usability and Preliminary Efficacy of Home-based FES Fro Adhesive Capsulitis is a clinical trial registered under NCT07227662. Current status: NOT_YET_RECRUITING.
What is the status of NCT07227662?
The current status of NCT07227662 (Feasibility, Usability and Preliminary Efficacy of Home-based FES Fro Adhesive Capsulitis) is: NOT_YET_RECRUITING.
When did Feasibility, Usability and Preliminary Efficacy of Home-based FES Fro Adhesive Capsulitis start?
Feasibility, Usability and Preliminary Efficacy of Home-based FES Fro Adhesive Capsulitis started on 2026-06-01.
Official Source
View on ClinicalTrials.gov →Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.