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Telerehabilitation for Stroke Rehabilitation (Telestroke Trial)

N/A
Recruiting
Research Sponsored by Université de Sherbrooke
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Have had stroke event (haemorrhagic or ischemic)
Have a relative or informal caregiver who is present in the home should physical rehabilitation treatments are required
Timeline
Screening 3 weeks
Treatment Varies
Follow Up through study completion (up to 5 years)
Awards & highlights

Telestroke Trial Summary

This trial aims to compare the effectiveness of telerehabilitation (live treatment sessions with an interdisciplinary group of clinicians via a telecommunication platform) versus usual care for patients who have experienced stroke.

Who is the study for?
This trial is for Canadian stroke survivors who are safe to go home and have mild to moderate independence. They must speak French or English, have a caregiver at home, and have had a recent stroke (hemorrhagic or ischemic). People with severe cognitive decline before the stroke cannot join.Check my eligibility
What is being tested?
The study tests if telerehabilitation—remote rehab sessions via technology—with team care plans improves recovery compared to usual care after a stroke. It involves 220 patients receiving this new approach versus 110 getting standard treatment.See study design
What are the potential side effects?
Since the intervention focuses on rehabilitation through technology rather than medication, side effects may include discomfort with tech use or issues related to remote communication rather than physical drug-related side effects.

Telestroke Trial Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
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I have had a stroke before.
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I have someone at home to help me if I need physical rehab.
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My care team believes I can safely go home.
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I can speak French or English.

Telestroke Trial Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~through study completion (up to 5 years)
This trial's timeline: 3 weeks for screening, Varies for treatment, and through study completion (up to 5 years) for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Change in patient adherence to stroke rehabilitation plan
Patient adherence to stroke rehabilitation plan (Patient journal)
Patient adherence to stroke rehabilitation plan (Professional perception)
Secondary outcome measures
Adverse events
Change in depression state
Change in functional recovery and independence
+9 more

Telestroke Trial Design

2Treatment groups
Experimental Treatment
Group I: TelerehabilitationExperimental Treatment1 Intervention
A mix of home or rehabilitation center visits, telerehabilitation and interprofessional shared decision making process.
Group II: ControlExperimental Treatment1 Intervention
Usual rehabilitation care (no telerehabilitation, interdisciplinary meetings not systematically organized and/or not involving a complete team of professionals)

Find a Location

Who is running the clinical trial?

Canadian Institutes of Health Research (CIHR)OTHER_GOV
1,340 Previous Clinical Trials
26,452,368 Total Patients Enrolled
Université de SherbrookeLead Sponsor
292 Previous Clinical Trials
69,111 Total Patients Enrolled
Université de MontréalOTHER
213 Previous Clinical Trials
102,391 Total Patients Enrolled

Media Library

Telerehabilitation and team meetings and team care plans Clinical Trial Eligibility Overview. Trial Name: NCT04440215 — N/A
Stroke Rehabilitation Research Study Groups: Control, Telerehabilitation
Stroke Rehabilitation Clinical Trial 2023: Telerehabilitation and team meetings and team care plans Highlights & Side Effects. Trial Name: NCT04440215 — N/A
Telerehabilitation and team meetings and team care plans 2023 Treatment Timeline for Medical Study. Trial Name: NCT04440215 — N/A

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

In how many locations is this trial being conducted?

"Currently, the study runs in 6 different geographical locations including Granby, Vaudreuil-Dorion, and Châteauguay. To reduce travel demands for those that join this trial, it is recommended to select a nearby site."

Answered by AI

What is the prime aim of this medical experiment?

"The primary endpoint of this research endeavour, which will be assessed over a predetermined period including baseline and 4-, 6- and 12-week post-recruitment time points is an evaluation of patient adherence to stroke rehabilitation plans (as perceived by medical professionals). Secondary endpoints encompass the collection of sociodemographic data gathered through home questionnaires covering sex, age, clinical info related to stroke; adverse events associated with rehab such as pain, dizziness or fatigue along with recorded falls; plus changes in social reintegration measured via the Reintegration to Normal Living Index. A high score reflects more difficulty readjusting back into normal life"

Answered by AI

What is the total number of participants accepted into this clinical research?

"Affirmative. Per the details available on clinicaltrials.gov, this medical experiment is actively adding participants -- initially posted on July 10th 2020 and most recently edited on July 15th 2021 -- with a requirement for 330 patients recruited from 6 distinct sites."

Answered by AI
~69 spots leftby Apr 2025