RECRUITING

MiGo Tracker Remote Monitoring of Home Exercise After Stroke

Description

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

Study Overview

Study Details

Study overview

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.

MiGo Tracker: Seamless Remote Therapeutic Monitoring of Exercise Adherence After Stroke

MiGo Tracker Remote Monitoring of Home Exercise After Stroke

Condition
Subacute Stroke
Intervention / Treatment

-

Contacts and Locations

Downey

Rancho Research Institute, Inc, Downey, California, United States, 90242

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility 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)
  • * 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

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Flint Rehabilitation Devices, LLC,

Study Record Dates

2026-08-31