Home-based intensive motor telerehabilitation with MindMotion GO for post-stroke arm weakness

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This single-center randomized controlled trial will randomize sub-acute and chronic stroke patients to a 12-week home-based telerehabilitation program using the MindMotion GO device in addition to standard care, delivering 300 minutes per week of active therapy. The program combines one synchronous weekly session with a therapist and multiple asynchronous autonomous sessions, with remote planning and monitoring. It is integrated into the post-stroke care pathway to ease the transition from hospital to home without prolonging hospitalization or increasing face-to-face visits. The trial will measure feasibility, adherence, and motor function outcomes compared with standard care.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Hospitalized for a first ischemic or hemorrhagic stroke
* Stroke occurrence more than 30 days prior
* Presenting motor deficits affecting the upper limb, with or without involvement of the lower limb
* Able to follow the instructions of the home program using the MindMotion GO device
* Having at home an accessible email address, an Internet connection with password, a smartphone, a screen or TV with HDMI input (Full HD 1080p resolution), and a free space of approximately 1 m x 2.5 m in front of the screen
* Ability to sit without assistance
* Patient agreeing to participate in the study by signing an informed consent form
* Affiliated with, or entitled to, a social security scheme

Exclusion Criteria:

History of stroke

* Neurological pathology other than stroke
* Patient with uncontrolled epilepsy or seizure disorder
* Cardiac disease limiting exercise
* Pain limiting rehabilitation dose
* Major comprehension problems or severe psychiatric and/or cognitive disorders that could compromise understanding of the protocol and the smooth running of the study.
* Uncorrected hearing or visual deficits
* Severe apraxia
* Severe memory impairment
* Severe unilateral spatial neglect
* Total plegia of affected limb
* Pregnant, parturient or breast-feeding women
* Persons deprived of their liberty by judicial or administrative decision
* Persons admitted to a health or social institution for purposes other than research
* Adults under legal protection (guardianship, curatorship)
* Subjects participating in other intervention research.

Where it's running

• Hopital Henry Gabrielle
  Saint-Genis-Laval, Lyon, France Recruiting

Study contacts

• Study coordinator: Jacques LUAUTÉ, MD
• Email: Jacques.luaute@chu-lyon.fr
• Phone: 4 78 86 50 64

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

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• Web-based therapy using action observation and mirror therapy for arm weakness after stroke

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• Dual-task balance training plus computer-based cognitive training after stroke

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  Recruiting Matia Foundation · San Sebastián, GUIPUZCOA · NCT07913620

How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.