MiGo Tracker remote monitoring to support home arm exercises after a stroke
Official title: MiGo Tracker: Seamless Remote Therapeutic Monitoring of Exercise Adherence After Stroke
Run by Flint Rehabilitation Devices, LLC · NCT06752707 · Data updated 2026-11-12
This program will test whether using the MiGo Tracker to remotely monitor home arm exercises helps people within 30 days after a stroke improve arm movement and stick with their exercises.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 50 (estimated) |
| Sponsor | Flint Rehabilitation Devices, LLC Industry-sponsored |
| Locations | 1 site (Downey, California) |
| Status | Recruiting |
| Started | June 11, 2025 |
| Main results expected | March 31, 2026 |
| Study ends | August 31, 2026 |
| Registry record updated | July 16, 2025 |
| Trial ID | NCT06752707 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are adults within 30 days of a stroke who have some upper-extremity movement (Fugl-Meyer >5 and ≤55), can follow two-step commands, and have no other major neurological or severe medical problems.
✕Probably not a fit
People under 18, those unable to follow two-step commands, those with other neurological diagnoses or serious concurrent illnesses, and those with very minimal or extremely severe arm impairment are unlikely to benefit from this program.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This is a randomized controlled trial enrolling 50 people with subacute stroke to compare a MiGo Tracker remote therapeutic monitoring (RTM) program versus a conventional home exercise prescription without monitoring. Participants will be randomly assigned to the MiGo RTM intervention or usual care and will continue to receive standard outpatient rehabilitation. The primary outcome is motor recovery measured three months after stroke, with safety and adherence tracked throughout the study. Eligible participants have had a stroke within 30 days and have measurable upper-extremity impairment based on Fugl-Meyer scores.
Why it matters
Potential benefit: If successful, the MiGo Tracker could increase home exercise adherence and improve arm motor recovery for many people after stroke.
How similar studies have gone: Wearable and remote-monitoring approaches for post-stroke rehabilitation have shown promising early results for improving adherence and activity, but large randomized evidence in the subacute period remains limited.
Who can join: the full rules
Show full inclusion / exclusion 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
Where it's running
-
Rancho Research Institute, Inc
Downey, California, United States Recruiting
Study contacts
- Study coordinator: Ian M Russell, PhD
- Email: irussell@flintrehab.com
- Phone: 3392232676
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.