Telerehabilitation Early After Stroke

NCT ID: NCT05625438

Last Updated: 2024-12-06

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: NA
• Total Enrollment: 20 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2022-12-19
• Study Completion Date: 2025-12-31

Brief Summary

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.

Detailed Description

This clinical trial is designed to address 3 specific aims:

Aim 1: To measure the safety of daily bedside telerehabilitation.

Aim 2: To measure the feasibility of daily bedside telerehabilitation.

Aim 3: To derive a preliminary estimate of motor and functional outcomes in patients engaged in daily bedside telerehabilitation.

Telerehabilitation therapy is delivered over the course of the inpatient rehabilitation stay. A therapist-facing web portal is used for treatment planning and patient monitoring. The treatment approach was initially designed based on an upper-extremity task-specific training manual and Accelerated Skill Acquisition Program.

Each daily 45-minute treatment session is created by a licensed OT or PT and includes:

A. At least 15 min/day of upper extremity exercises. In addition, therapists have the option to incorporate standard exercise equipment (e.g., Theraband or dowels) that can be incorporated into assigned exercises.

B. At least 15 min/day of functional training through games. The study provides 2 controllers with 5 different input devices that are available to drive game play. Games stress various motor control features (e.g., varying movement speed, range of motion, target size, extent of visuomotor tracking, or level of cognitive demand), which are selected and adjusted by the therapist.

C. Five minutes/day of stroke education. The education content targets five categories (Stroke Risk Factors, Stroke Prevention, Effects of Stroke, Diet, and Exercise) and corresponds to the Stroke Knowledge Exam.

Conditions

Cerebral Stroke

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Bedside Telerehabilitation

Participants will be assigned 45-minute therapy training exercises each day for 5 days per week.

Participants will use the HandyMotion device to interact with the telerehabilitation program displayed on the TV set in the patient room.

Group Type: EXPERIMENTAL

HandyMotion Treatment Program

Intervention Type: DEVICE

A pair of sensor-based wireless remote controllers to allow the performance of functional exercises and games that target arm movement.

Interventions

HandyMotion Treatment Program

A pair of sensor-based wireless remote controllers to allow the performance of functional exercises and games that target arm movement.

Intervention Type: DEVICE

Eligibility Criteria

Inclusion 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

Exclusion Criteria

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

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Providence St. Jude Medical Center

UNKNOWN

Sponsor Role: collaborator

TRCare, Inc.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Natalia Covarrubias-Eckardt, MD

Role: PRINCIPAL_INVESTIGATOR

Providence St. Jude Medical Center

Locations

Providence St. Jude Medical Center

Fullerton, California, United States

Site Status: RECRUITING

Countries

United States

Central Contacts

Johnson K Sun

Role: CONTACT

Phone: 650-300-2168

Email: kit@trcare.net

Facility Contacts

Natalia Covarrubias-Eckardt, MD

Role: primary

Other Identifiers

TRC-08

Identifier Type: -

Identifier Source: org_study_id