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NCT07227662 · ClinicalTrials.gov registry record · NA
Feasibility, Usability and Preliminary Efficacy of Home-based FES Fro Adhesive Capsulitis
A NA study, sponsored by University of Maryland, Baltimore.
- Not yet
- Registry status
- NA
- Development phase
- 10
- Enrollment target
NCT07227662: Clinical Trial NA study, sponsored by University of Maryland, Baltimore.
NCT07227662 is a NA study that has not yet begun recruiting, run by University of Maryland, Baltimore. The registered enrollment target is 10 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT07227662, a NA study, has not yet begun recruiting, sponsored by University of Maryland, Baltimore.
- NOT YET RECRUITING
- Registry status
- NA
- Development phase
- 10 participants
- Enrollment target
Study 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.
Primary Outcome
Participant-reported satisfaction, comfort, and ease of use assessed using a 5-point Likert scale and open-ended qualitative feedback.A Likert scale is a rating scale used in surveys to measure opinions, attitudes,and perceptions by asking respondents to indicate their level of agreement or disagreement with a statement. It consists of a series of statements with a symmetric range of response options, such as a five-point scale from 0="Strongly Disagree" to 5="Strongly Agree". This method allows
Interventions
- DEVICE Home based FES in combination with usual therapy
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 10 participants |
| Start Date | 2026-06-01 |
| Est. Completion | 2026-12-01 |
| Phase | NA |
What is known before NCT07227662 opens enrollment
NCT07227662 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 10 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower).
The record links to 0 conditions, and to 1 intervention - of which Home based FES in combination with usual therapy is the first listed.
NCT07227662 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT07227662 about?
NCT07227662 is a clinical study titled "Feasibility, Usability and Preliminary Efficacy of Home-based FES Fro Adhesive Capsulitis". 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 w...
What is the current status of trial NCT07227662?
This trial is currently not yet recruiting. It is a NA study. The enrollment target is 10 participants. The study started on 2026-06-01. Estimated completion is 2026-12-01.
What interventions are being tested in trial NCT07227662?
The interventions under investigation include: Home based FES in combination with usual therapy (DEVICE).
Who is sponsoring clinical trial NCT07227662?
This trial is sponsored by University of Maryland, Baltimore, which has 560 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT07227662's enrollment target sits among peer trials
10 1927th of 2000 higher than 26 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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