Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT05625438

Telerehabilitation Early After Stroke

Led by TRCare, Inc. · Updated on 2024-12-06

20

Participants Needed

1

Research Sites

154 weeks

Total Duration

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Sponsors

T

TRCare, Inc.

Lead Sponsor

P

Providence St. Jude Medical Center

Collaborating Sponsor

AI-Summary

What this Trial Is About

The goal of this clinical trial is to assess the safety and feasibility of providing extra doses of rehabilitation therapy for persons with a recent stroke. The therapy treatment targets to improve arm function by introducing telerehabilitation to the bedside of participants during the inpatient rehab admission period. Participants will use a newly developed functional training system (HandyMotion) to access therapy treatment program directly from their hospital room. HandyMotion is a sensor-based training system that can connect to the TV set in the hospital room, enabling patients to access their therapy training program to practice rehab-oriented games and exercises ad libitum, at any time of the day.

CONDITIONS

Official Title

Telerehabilitation Early After Stroke

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older
  • Stroke verified by imaging due to ischemia or intracerebral hemorrhage within 30 days before enrollment, or traumatic brain injury
  • Unilateral arm motor deficits with affected arm Box & Block Test score of at least 1 block in 60 seconds and no more than 90% of the good arm
  • Enough arm movement to participate in therapy
  • Signed informed consent
  • Able to follow simple instructions
  • Participation not significantly limited by agitated behavior
Not Eligible

You will not qualify if you...

  • Major, active neurological or psychiatric disease likely to limit participation, such as advanced dementia
  • Cognitive status expected to interfere substantially with playing assigned games or exercises
  • Communication deficits interfering with reasonable study participation
  • Visual acuity worse than 20/50 in both eyes, with or without correction
  • Insufficient English to comply with study procedures
  • Shoulder pain likely to substantially limit telerehabilitation therapy completion as judged by study team

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Providence St. Jude Medical Center

Fullerton, California, United States, 92835

Actively Recruiting

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Research Team

J

Johnson K Sun

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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