MiGo Tracker Remote Monitoring of Home Exercise After Stroke

Last updated: July 11, 2025
Sponsor: Flint Rehabilitation Devices, LLC
Overall Status: Active - Recruiting

Phase

N/A

Condition

Stroke

Cerebral Ischemia

Treatment

MiGo Tracker

Conventional home exercise program

Clinical Study ID

NCT06752707
R44AG090216-01
R44AG090216-01
  • Ages > 18
  • All Genders

Study Summary

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.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • 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)

Exclusion

Exclusion Criteria:

  • 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 fromcompleting the 3-month study

Study Design

Total Participants: 50
Treatment Group(s): 2
Primary Treatment: MiGo Tracker
Phase:
Study Start date:
June 11, 2025
Estimated Completion Date:
August 31, 2026

Connect with a study center

  • Rancho Research Institute, Inc

    Downey, California 90242
    United States

    Active - Recruiting

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