MiGo Tracker Remote Monitoring of Home Exercise After Stroke
Flint Rehabilitation Devices, LLC · with National Institute on Aging (NIA), Rancho Research Institute, Inc. · NCT06752707
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18+ · All sexes
- Healthy volunteers
- Not accepted (a condition is required)
- Study type
- Interventional · Not applicable
- Target enrollment
- 50
- US sites recruiting
- 1
- Study start
- June 11, 2025
- Record last updated
- July 16, 2025
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study 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.
Being studied: MiGo Tracker; Conventional home exercise program
Conditions: Subacute Stroke
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
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 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 from completing the 3-month study
Recruiting US locations
Rancho Research Institute, Inc
Downey, CA 90242
Site contact: Nicole Bayus · 562-385-7049 · NicoleB@ranchoresearch.org
Study contacts (from the official record)
- Ian M Russell, PhD · 3392232676 · irussell@flintrehab.com
- Daniel Zondervan, PhD · 949-313-7322 · dzondervan@flintrehab.com
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