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NCT06207240 · ClinicalTrials.gov registry record · NA
Functional Electrical Stimulation Therapy After Stroke
A NA study, sponsored by Battelle Memorial Institute.
- Completed
- Registry status
- NA
- Development phase
- 2
- Enrollment target
NCT06207240 is a NA study that has completed, run by Battelle Memorial Institute. The registered enrollment target is 2 participants.
The verdict
NCT06207240, a NA study, has completed, sponsored by Battelle Memorial Institute.
- COMPLETED
- Registry status
- NA
- Development phase
- 2 participants
- Enrollment target
Study Summary
The goal of this feasibility study is to test the feasibility of providing task-oriented, intention-driven functional electrical stimulation (FES) using the novel NeuroLife FES Sleeve and NeuroLife electromyography (EMG) and FES Sleeve devices in chronic stroke survivors. The main questions it aims to answer are: * Can these devices be used to administer task-oriented therapy with assistive stimulation at similar doses to current standards of care? * How does therapy using these devices impact the upper limb function in a few chronic stroke survivors? Participants will receive assistive electrical stimulation synchronized to their movement intention while practicing functional tasks with everyday objects over the course of 8 weeks.
Interventions
- DEVICE NeuroLife FES Sleeve / NeuroLife EMG-FES Sleeve
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 2 participants |
| Start Date | 2022-01-18 |
| Est. Completion | 2022-06-08 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06207240
The ClinicalTrials.gov registry entry for NCT06207240 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 2 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Battelle Memorial Institute, which has 8 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which NeuroLife FES Sleeve / NeuroLife EMG-FES Sleeve is the first listed.
NCT06207240 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT06207240 about?
NCT06207240 is a clinical study titled "Functional Electrical Stimulation Therapy After Stroke". The goal of this feasibility study is to test the feasibility of providing task-oriented, intention-driven functional electrical stimulation (FES) using the novel NeuroLife FES Sleeve and NeuroLife electromyography (EMG) and FES Sleeve devices in chronic stroke survivors. The main questions it aims ...
What is the current status of trial NCT06207240?
This trial is currently completed. It is a NA study. The enrollment target is 2 participants. The study started on 2022-01-18. Estimated completion is 2022-06-08.
What interventions are being tested in trial NCT06207240?
The interventions under investigation include: NeuroLife FES Sleeve / NeuroLife EMG-FES Sleeve (DEVICE).
Who is sponsoring clinical trial NCT06207240?
This trial is sponsored by Battelle Memorial Institute, which has 8 total clinical trials registered on ClinicalTrials.gov.
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