MiGo Tracker Remote Monitoring of Home Exercise After Stroke

Recruiting now · Not applicable

Conditions studied: Subacute Stroke

In brief

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.

Key facts

Study ID

NCT06752707

Run by

Flint Rehabilitation Devices, LLC

People needed

50

Starts

2025-06-11

Expected to finish

2026-08-31

Last updated by the study team

2025-07-16

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Experienced one or more strokes less than one month (30 days) prior
• Upper Extremity Fugl-Meyer Score > 5 and <= 55 out of 66
• Absence of moderate to severe pain (<= 4 on the 10 point visual-analog pain scale)

You may not qualify if…

• age <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

Where it is running

• Rancho Research Institute, Inc — Downey, California, United States (enrolling)

Full record on ClinicalTrials.gov

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