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MiGo Tracker for Home Exercise After Stroke

This study is testing a device called the MiGo Tracker to see if it helps people recover better after a stroke. You might be able to join if you've had a stroke less than one month ago and have some movement in your arm (Upper Extremity Fugl-Meyer Score between 5 and 55). Participants will be randomly assigned to either use the MiGo Tracker during home exercises or follow a standard home exercise program with printed sheets. All participants will still receive their usual stroke care, like outpatient therapy. The main goal is to see if using the MiGo Tracker leads to better arm movement recovery three months after your stroke. The study plans to enroll 50 people, but its current recruitment status is unclear.

Study design
This is an interventional study with 50 participants. You would be randomly assigned to one of two groups: using the MiGo Tracker or a conventional home exercise program.
What's involved
You would perform home exercise sessions while wearing the MiGo Tracker device, which logs exercise data, or follow exercises from printed sheets.
Compensation
Not stated in the trial record.
Follow-up
Your arm movement will be measured at the start of the study and again three months after your stroke.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT06752707

MiGo Tracker Remote Monitoring of Home Exercise After Stroke

Recruiting
NAAges 18+InterventionalTreatment
Flint Rehabilitation Devices, LLC
~50 participants
Updated 2025-07-16 on ClinicalTrials.gov
What's tested:MiGo TrackerConventional home exercise program

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Change in Upper Extremity Fugl-Meyer from Baseline
Measured over Baseline and 3 months post stroke

Conditions

Subacute Stroke

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NCT06752707

Where you'd take part

This study runs at 1 site. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.

  • Rancho Research Institute, Inc

    Downey, Californiastudy coordinator listed

    Recruiting

Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.

Who to contact

Ian M Russell, PhD
[email protected]
3392232676
Email the study team

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Eligibility criteria

Inclusion

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

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

What this trial measures

  • Change in Upper Extremity Fugl-Meyer from BaselineBaseline and 3 months post stroke

    The Fugl-Meyer Assessment - Upper Extremity (FMA-UE) is a stroke-specific, performance-based impairment index. It is designed to assess motor functioning, sensation, balance, joint range of motion and joint pain in patients with post-stroke hemiplegia. A standardized assessment of arm impairment based on scores of 0-2 on 33 different tasks. Minimum value = 0, maximum value = 66, higher scores = better outcome