RECRUITING

Telerehabilitation Early After Stroke

Conditions

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Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

Bedside Telerehabilitation Early After Stroke

Quick Facts

Study Start:2022-12-19

Study Completion:2025-12

Study Type:Not specified

Phase:Not Applicable

Enrollment:Not specified

Status:RECRUITING

Study ID

NCT05625438

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years

Sexes Eligible for Study:ALL

Accepts Healthy Volunteers:No

Standard Ages:ADULT, OLDER_ADULT

Inclusion Criteria	Exclusion Criteria
1. Age 18 years or older 2. Stroke that is radiologically verified, due to ischemia or to intracerebral hemorrhage, and with time of stroke onset \<30 days prior to enrollment; or traumatic brain injury. 3. Unilateral arm motor deficits that are neither trivial (no arm weakness) or devastating (arm plegia). This requires that the baseline Box \& Block Test score with affected arm to be at least 1 block in 60 seconds but no more than 90% of the number of blocks with the good arm. 4. Possess enough arm movement to participate in therapy 5. Informed consent signed by the subject 6. Able to follow simple instructions 7. Study participation is not likely to be significantly limited by agitated behavior	1. A major, active, coexistent neurological or psychiatric disease that would limit study participation, e.g., advanced dementia 2. Expectation that patient's cognitive status will likely interfere substantially with playing assigned games or exercises 3. Deficits in communication that interfere with reasonable study participation 4. Lacking visual acuity, with or without corrective lens, of 20/50 or better in at least one eye 5. Subject does not speak sufficient English to comply with study procedures 6. Shoulder pain that in the judgement of the study team is likely to substantially limit the amount of telerehabilitation therapy completed

Inclusion Criteria

Exclusion Criteria

1. Age 18 years or older
2. Stroke that is radiologically verified, due to ischemia or to intracerebral hemorrhage, and with time of stroke onset \<30 days prior to enrollment; or traumatic brain injury.
3. Unilateral arm motor deficits that are neither trivial (no arm weakness) or devastating (arm plegia). This requires that the baseline Box \& Block Test score with affected arm to be at least 1 block in 60 seconds but no more than 90% of the number of blocks with the good arm.
4. Possess enough arm movement to participate in therapy
5. Informed consent signed by the subject
6. Able to follow simple instructions
7. Study participation is not likely to be significantly limited by agitated behavior

1. A major, active, coexistent neurological or psychiatric disease that would limit study participation, e.g., advanced dementia
2. Expectation that patient's cognitive status will likely interfere substantially with playing assigned games or exercises
3. Deficits in communication that interfere with reasonable study participation
4. Lacking visual acuity, with or without corrective lens, of 20/50 or better in at least one eye
5. Subject does not speak sufficient English to comply with study procedures
6. Shoulder pain that in the judgement of the study team is likely to substantially limit the amount of telerehabilitation therapy completed

Contacts and Locations

Study Contact

Johnson K Sun

CONTACT

650-300-2168

kit@trcare.net

Principal Investigator

Natalia Covarrubias-Eckardt, MD

PRINCIPAL_INVESTIGATOR

Providence St. Jude Medical Center

Study Locations (Sites)

Providence St. Jude Medical Center

Fullerton, California, 92835

United States

Collaborators and Investigators

Sponsor: TRCare, Inc.

Natalia Covarrubias-Eckardt, MD, PRINCIPAL_INVESTIGATOR, Providence St. Jude Medical Center

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2022-12-19

Study Completion Date2025-12

Study Record Updates

Study Start Date2022-12-19

Study Completion Date2025-12

Terms related to this study

Additional Relevant MeSH Terms

Cerebral Stroke