Gamification of Neurorehabilitation-centric Hand Exercises Post Stroke or Brain Injury

Last updated: March 31, 2023
Sponsor: IRegained Inc.
Overall Status: Active - Recruiting

Phase

N/A

Condition

Stroke

Cerebral Ischemia

Neurologic Disorders

Treatment

N/A

Clinical Study ID

NCT05547217
LUSUON0002
  • Ages 25-85
  • All Genders

Study Summary

Stroke is the leading cause of adult disability worldwide. Often, severe neurological deficits occur after a stroke and roughly 70% of all stroke survivors have some form of hand function disability. To improve the lives of those with hand function disability, IRegained Inc. has created the MyHandTM System. The MyHandTM System is a smart-mechatronic device programmed with proprietary hand function training regiments (protocols) based on deep research in neuroplasticity. It provides a highly unique and targeted approach to hand function rehabilitation with the help of the aforementioned protocols delivered with gamified training techniques. The gamified format of the protocols allows for better patient engagement, thus allowing for more effective and efficient therapy. Individuals who have sustained a stroke 5 months or earlier (considered to be chronic stroke survivors) will be eligible to participate in this study. Participants will undergo a 2-hour training session, 2-3 days per week, over 12 weeks, for a total of 30 sessions. Hand function therapy will be administered in a specific and gamified manner to enhance rehabilitation of the hand and provide participants with greater opportunity to regain hand function over the course of the study. The goal of this research project is to understand how a gamified approach to hand function rehabilitation impacts engagement and motivation. This understanding will directly translate into the development of more efficient and effective modes of therapy.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Sustained a single stroke

Exclusion

Exclusion Criteria:

  • Severe spasticity or contractures (2 or less in the CMSA) or any other musculoskeletalor neuromuscular disorders that compromise sensation or other neuromuscular parameterswill be excluded from the study. Prospective participants who are incapable ofproviding consent to participate in the research study will also be excluded (determined by an MMSE score of 23 or less).

Study Design

Total Participants: 8
Study Start date:
September 19, 2022
Estimated Completion Date:
September 19, 2023

Connect with a study center

  • Laurentian University

    Sudbury, Ontario P3E 2C6
    Canada

    Active - Recruiting

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