MiGo Tracker remote monitoring to support home arm exercises after a stroke
MiGo Tracker: Seamless Remote Therapeutic Monitoring of Exercise Adherence After Stroke
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
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 50 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Flint Rehabilitation Devices, LLC Industry-sponsored |
| Locations | 1 site (Downey, California) |
| Trial ID | NCT06752707 on ClinicalTrials.gov |
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.
Who should consider this trial
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.
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.
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 performed: 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.
Eligibility criteria
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 this trial is running
Downey, California
- Rancho Research Institute, Inc — Downey, California, United States (Recruiting)
Study contacts
- Study coordinator: Ian M Russell, PhD
- Email: irussell@flintrehab.com
- Phone: 3392232676
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.