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NCT03663361 · ClinicalTrials.gov registry record · NA
Addressing Neuromuscular Deficits for Improved Outcomes in Ankle Rehabilitation
A NA study of Ankle Sprains, sponsored by Phillip Gribble.
- Recruiting
- Registry status
- NA
- Development phase
- 150
- Enrollment target
- 2
- Study locations
NCT03663361: Recruiting NA study of Ankle Sprains, sponsored by Phillip Gribble.
NCT03663361 is a NA study of Ankle Sprains that is actively recruiting participants, run by Phillip Gribble. The registered enrollment target is 150 participants, below the 222-participant average among 4 other Ankle Sprains trials with a reported enrollment target (32% lower). The trial reports 2 study locations across 2 states. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT03663361, a NA study of Ankle Sprains, is actively recruiting participants, sponsored by Phillip Gribble.
- RECRUITING
- Registry status
- NA
- Development phase
- 150 participants
- Enrollment target
- 2
- Study locations
Study Summary
The purpose of this project is to compare a novel sensorimotor ankle rehabilitation training (SMART) protocol for Lateral ankle sprains (LASs) against a standard of care (SOC) protocol to determine if it is more successful at producing successful one-year outcomes and lower rates of re-injury and improved health. This will address the identified needs for evidence-support and reintegration strategies to improve understanding of the management of patient rehabilitation strategies throughout the rehabilitation process following neuromusculoskeletal injury. The project will validate an innovative rehabilitation approach while providing metrics of success using a variety of clinical and innovative markers.
Primary Outcome
The number of patient reported re-sprains of the ankle. The outcomes will be assessed at 12 months post-rehabilitation discharge (ie. return to activity).
Conditions Studied
Interventions
- OTHER SMART Intervention
- OTHER Standard of Care Intervention
Study Locations (2)
Kentucky
- University of Kentucky - Lexington
North Carolina
- University of North Carolina at Chapel Hill - Chapel Hill
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 150 participants |
| Start Date | 2019-11-12 |
| Est. Completion | 2026-07 |
| Phase | NA |
What NCT03663361 shows while recruiting
NCT03663361 is an interventional study that assigns participants to a tested intervention. The registered 150 participants enrollment target is mid-sized for trials with a published cap, below the 222-participant average among 4 other Ankle Sprains trials with a reported enrollment target (32% lower).
The record links to 1 condition, with Ankle Sprains appearing as the primary indexed condition, and to 2 interventions - of which SMART Intervention is the first listed.
NCT03663361 reports a single indexed study location in Kentucky, North Carolina.
Frequently Asked Questions
What is clinical trial NCT03663361 about?
NCT03663361 is a clinical study titled "Addressing Neuromuscular Deficits for Improved Outcomes in Ankle Rehabilitation". The purpose of this project is to compare a novel sensorimotor ankle rehabilitation training (SMART) protocol for Lateral ankle sprains (LASs) against a standard of care (SOC) protocol to determine if it is more successful at producing successful one-year outcomes and lower rates of re-injury and im...
What is the current status of trial NCT03663361?
This trial is currently recruiting. It is a NA study. The enrollment target is 150 participants. The study started on 2019-11-12. Estimated completion is 2026-07.
What conditions does trial NCT03663361 study?
This clinical trial studies the following conditions: Ankle Sprains.
What interventions are being tested in trial NCT03663361?
The interventions under investigation include: SMART Intervention (OTHER), Standard of Care Intervention (OTHER).
Who is sponsoring clinical trial NCT03663361?
This trial is sponsored by Phillip Gribble, which has 1 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT03663361 being conducted?
This trial has 2 study locations across Kentucky, North Carolina. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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