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NCT05423600 · ClinicalTrials.gov registry record · NA
Transspinal Stimulation With and Without Blood Flow Restricted Exercise Via Telehealth in Persons With Tetraplegia
A NA study of Tetraplegia/Tetraparesis, sponsored by Virginia Commonwealth University.
- Recruiting
- Registry status
- NA
- Development phase
- 44
- Enrollment target
- 3
- Study locations
NCT05423600: Recruiting NA study of Tetraplegia/Tetraparesis, sponsored by Virginia Commonwealth University.
NCT05423600 is a NA study of Tetraplegia/Tetraparesis that is actively recruiting participants, run by Virginia Commonwealth University. The registered enrollment target is 44 participants, above the 36-participant average among 9 other Tetraplegia/Tetraparesis trials with a reported enrollment target (22% higher). The trial reports 3 study locations across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT05423600, a NA study of Tetraplegia/Tetraparesis, is actively recruiting participants, sponsored by Virginia Commonwealth University.
- RECRUITING
- Registry status
- NA
- Development phase
- 44 participants
- Enrollment target
- 3
- Study locations
Study Summary
The purpose of the current study is to evaluate whether a home-based, telehealth-supported intervention combining Blood Flow Restricted Exercise (BES) and Transspinal Stimulation (TS) will improve motor and functional abilities greater than BES+sham TS in persons with chronic, incomplete tetraplegia.
Primary Outcome
The grasp and release test is a standardized test of functional activities depending on hand function in persons with cSCI. Participants will be asked to lift and move a peg, block, can, 1 lb. dumbbell weight and fork from lateral to medial over a 60 cm distance and release at midline.
Conditions Studied
Interventions
- PROCEDURE BES + TS
- PROCEDURE Experimental: BES+sham TS
Study Locations (3)
Virginia
- Sheltering Arms Physical Rehabilitation Centers - Richmond
- Richmond VA Medical Center - Richmond
- Virginia Commonwealth University - Richmond
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 44 participants |
| Start Date | 2022-06-15 |
| Est. Completion | 2026-09 |
| Phase | NA |
What NCT05423600 shows while recruiting
NCT05423600 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 44 participants, a relatively small participant target, above the 36-participant average among 9 other Tetraplegia/Tetraparesis trials with a reported enrollment target (22% higher).
The record links to 1 condition, with Tetraplegia/Tetraparesis appearing as the primary indexed condition, and to 2 interventions - of which BES + TS is the first listed.
NCT05423600 reports a single indexed study location in Virginia.
Frequently Asked Questions
What is clinical trial NCT05423600 about?
NCT05423600 is a clinical study titled "Transspinal Stimulation With and Without Blood Flow Restricted Exercise Via Telehealth in Persons With Tetraplegia". The purpose of the current study is to evaluate whether a home-based, telehealth-supported intervention combining Blood Flow Restricted Exercise (BES) and Transspinal Stimulation (TS) will improve motor and functional abilities greater than BES+sham TS in persons with chronic, incomplete tetraplegia...
What is the current status of trial NCT05423600?
This trial is currently recruiting. It is a NA study. The enrollment target is 44 participants. The study started on 2022-06-15. Estimated completion is 2026-09.
What conditions does trial NCT05423600 study?
This clinical trial studies the following conditions: Tetraplegia/Tetraparesis.
What interventions are being tested in trial NCT05423600?
The interventions under investigation include: BES + TS (PROCEDURE), Experimental: BES+sham TS (PROCEDURE).
Who is sponsoring clinical trial NCT05423600?
This trial is sponsored by Virginia Commonwealth University, which has 558 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT05423600 being conducted?
This trial has 3 study locations across Virginia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Tetraplegia/Tetraparesis
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT05423600's enrollment target sits among peer trials
44 3rd of 9 higher than 7 of 9 other Tetraplegia/Tetraparesis trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Tetraplegia/Tetraparesis 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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