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REEV SENSE for Gait Analysis in Post-stroke Gait Impairment (SENS-AG)

Study on walking patterns after stroke using REEV SENSE technology.

Recruiting
18 years and older
Non-Binary
Phase 3/4
  • Simplified description (AI rewritten)
  • Technical description (Original)

Study Overview: This research is looking at how well a device called REEV SENSE works for people who have trouble walking after a stroke. The device attaches to your leg or foot and helps doctors understand how you walk using a mobile app.

Who Can Join?

  • Adults 18 or older who had a stroke over six months ago.
  • Must be able to walk on your own, with or without a cane or walker.
  • Cannot join if you can't give consent or understand the tests.

The study happens at the MIT Center for Clinical and Translational Research. You'll walk back and forth for about 15 minutes while the device and another system record your movements. You can rest whenever you need to.

Key Points:

  • The study takes about 15 minutes to complete.
  • Only one visit is required.
  • No medication or treatment is involved, just walking with the device.
Study details
    Gait Disorders
    Neurologic

NCT1270

REEV LLC

1 April 2026

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Informed consent
Introduction
You are being asked to participate in a research study. Before you decide to participate in this study, it is important that you understand why the research is being done and what it will involve. This form is designed to give you the information about the study so you can decide whether to be in the study or not. Please take the time to read the following information carefully. You should ask the researcher if there is anything that is not clear or if you need more information.
Study Participation
If you agree to participate in this study, you will be asked to:
  • Attend screening visit to determine eligibility
  • Attend 6–8 clinic visits over approximately 12 weeks
  • Provide blood samples at designated visits
  • Complete questionnaires about your symptoms and quality of life
  • Take study medication or placebo as directed
  • Report any side effects or health changes to the study team

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