Actively Recruiting
MiGo Tracker Remote Monitoring of Home Exercise After Stroke
Led by Flint Rehabilitation Devices, LLC · Updated on 2025-07-16
50
Participants Needed
1
Research Sites
63 weeks
Total Duration
On this page
Sponsors
F
Flint Rehabilitation Devices, LLC
Lead Sponsor
N
National Institute on Aging (NIA)
Collaborating Sponsor
AI-Summary
What this Trial Is About
This project will determine the safety and effectiveness of a MiGo Tracker RTM program in a randomized controlled trial with individuals with subacute stroke (N=50). Participants will be randomly assigned to either the MiGo Tracker RTM program (intervention group) or prescription of home exercises with no monitoring (usual care/control group). All participants will still receive usual post-stroke care, including outpatient rehabilitation. The main question this study aims to answer is: Does a MiGo Tracker RTM program lead to significantly greater motor recovery at three-months post stroke than the usual care group. If successful, MiGo Tracker will lead to increased home exercise adherence and improved health outcomes for thousands of individuals following stroke.
CONDITIONS
Official Title
MiGo Tracker Remote Monitoring of Home Exercise After Stroke
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Experienced one or more strokes less than one month (30 days) prior
- Upper Extremity Fugl-Meyer Score greater than 5 and less than or equal to 55 out of 66
- Absence of moderate to severe pain (4 or less on the 10 point visual-analog pain scale)
You will not qualify if you...
- Age less than 18 years old
- Unable to follow 2-step commands
- Other neurological diagnosis (e.g. Parkinson's Disease)
- Other severe concurrent medical conditions that may prevent the participants from completing the 3-month study
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Rancho Research Institute, Inc
Downey, California, United States, 90242
Actively Recruiting
Research Team
I
Ian M Russell, PhD
CONTACT
D
Daniel Zondervan, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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