Recruiting

Telerehabilitation Tenzr

Sponsor:

University of Alberta

Code:

NCT07467785

Conditions

Stroke

Eligibility Criteria

Sex: All

Age: 18 - 70+

Healthy Volunteers: Not accepted

Interventions

Standard of Care (SOC)

Telerehabilitation with Tenzr

Study Details

Brief summary:

After a stroke, many people have trouble using their arms and hands. This can make daily tasks-like eating, dressing, or writing-very hard. In Alberta, especially in small towns and rural areas, many stroke survivors go home from the hospital without being referred to rehabilitation. As a result, they miss out on therapy that could help them get better.

This project will test a new way to bring rehabilitation directly into people's homes using telerehabilitation. We will work with 200 stroke survivors across Alberta who did not get regular outpatient rehab. Participants will use the clinically validated Tenzr system-a set of fun, game-like exercises with wearable sensors. Therapists will check in and guide them remotely.

When participants are enrolled in the study, they will be randomized (1:1) into two groups. The Immediate group will receive 8 weeks of home-based telerehabilitation using the Tenzr platform immediately after baseline, while the Delayed group will receive 8 weeks of observation (usual care) followed by 8 weeks of the same telerehabilitation intervention. Everyone in the study will be tested at the baseline, 8 weeks, and 16 weeks. At 16 weeks, we will also interview them to gather their feedback on the telerehabilitation. We want to learn if this program helps people improve arm and hand movement, if it's easy to use, and if people like it. We also want to see if it could be offered more widely across Alberta in the future.

The goal is to give more people access to stroke rehabilitation, no matter where they live.

Conditions

Stroke

Study ID

NCT07467785

Start date

Jun 2, 2026

Status verified date

Jun, 2026

Completion date

Aug, 2028

Anticipated

Primary completion date

Dec, 2027

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18 - 70+

Healthy Volunteers: Not accepted

Inclusion Criteria:

1. Not currently referred to, or participating in, upper extremity outpatient rehabilitation.
2. A confirmed stroke diagnosis (ischemic or hemorrhagic)
3. Have moderate-to-severe upper limb impairment
4. Live at home
5. Have access to internet and appropriate devices to have a virtual assessment with clinicians.
6. ≥ 18 years of age

Exclusion Criteria:

1. Referred to or currently participating in upper extremity outpatient rehabilitation.
2. Severe cognitive, communication, or medical comorbidities that would preclude safe home-based exercise
3. Don't have access to internet and appropriate devices to have a virtual assessment with clinicians.
4. < 18 years of age

Study Design

Enrollment

200 participants

Anticipated

Allocation

Randomized

Intervention Model

Crossover

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

active comparator: Immediate Group

The Immediate group will receive 8 weeks of home-based telerehabilitation using the Tenzr platform immediately after baseline clinical assessments.

active comparator: Delayed Group

Delayed group will receive 8 weeks of observation (usual care) following the baseline clinical assessment; followed by 8 weeks of the same telerehabilitation intervention.

Interventions

Standard of Care (SOC)

8 weeks of standard of care for patients discharged from hospital without referrals to outpatient rehabilitation.

Telerehabilitation with Tenzr

8 weeks of telerehabilitation at home supported by a remote therapist utilizing the Tenzr application.

Primary outcome measure

  • Change in Upper Extremity Fugl-Meyer Assessment for Upper Extremity (FM-UE) [ Time Frame: Baseline, 8 weeks and 16 weeks. ]

Central Contacts and Locations

Central contacts

Jessica M D'Amico, Scientific Program Lead and Assistant Professor, PhD

780-203-9478damico1@ualberta.ca

Yoshino Okuma, BScRN, MSc

yokuma@ualberta.ca

Locations

Glenrose Rehabilitation Hospital

Recruiting

Edmonton, Alberta, Canada, T5G 0B7

Contacts

Jessica M D'Amico, Scientific Program Lead, Assistant Professor, PhD

damico1@ualberta.ca

Yoshino Okuma, BScRN, MSc

yokuma@ualberta.ca

Principal Investigator:

Jessica M D'Amico, PhD

More Information

Sponsor

University of Alberta

Last update posted

Jun 3, 2026

Last verified

Jun, 2026

Keywords

  • rehabilitation
  • telerehabilitation
  • neurorecovery

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by University of Alberta on 2026-06-03.