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Tele-Rehabilitation Study for People With a History of Stroke

Tele-rehabilitation for Cognitive Disability Post Stroke: Enhancing Function in the Face of Geographical Disparities

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02724813
Enrollment
24
Registered
2016-03-31
Start date
2015-11-30
Completion date
2017-12-31
Last updated
2018-02-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stroke

Brief summary

Stroke results in long-term disability for many people, and particularly for survivors of stroke who have cognitive impairments. However, a decreasing proportion of stroke patients are able to access or receive publicly funded rehabilitation. The investigators have shown in previous studies that in-person delivery of the Cognitive Orientation to daily Occupational Performance (CO-OP) rehabilitation approach to promoting attainment of everyday life goals has resulted in improvements in functional independence and executive function. In a small pilot study of tele-CO-OP with people with chronic traumatic brain injury (TBI) (n=3), the investigators found the delivery method was feasible and that participants were satisfied with the treatment and demonstrated clinically significant improvements on personally meaningful activities. The investigators will investigate the feasibility, preliminary efficacy, and cost-effectiveness of delivering CO-OP in an online format to reduce disability post-stroke. The study design is a single-blind (assessor), randomized wait-list control trial with a one-month retention follow-up. All therapy and testing sessions will be delivered online. We hypothesize that participants will demonstrate improvement in everyday activities and community participation.

Interventions

BEHAVIORALCognitive Orientation to Occupational Preformance (COOP)

Sponsors

Health and Stroke Foundation-Canadian Partnership for Stroke recovery
CollaboratorUNKNOWN
Baycrest
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

* Community-dwelling adults at least three months post-stroke * Fluent in written and spoken English * Impairment of executive cognitive functions * Ability to self-identify specific areas of difficulty in their everyday life that they would like to improve * Access to a computer or tablet with a high-speed internet connection

Exclusion criteria

* Presence of dementia * Severe concurrent depression * Severe aphasia * Concurrent substance abuse

Design outcomes

Primary

MeasureTime frameDescription
Changes in Canadian Occupational Performance Measure (COPM)10 weeks and 14 weeksThe COPM is a standardized, semi-structured interview that facilitates goal identification and has been used as the primary outcome measure for many of the CO-OP studies
Changes in Reintegration to Normal Living Index (RNL)10 weeks and 14 weeksThe RNL is a measure of satisfaction with participation in everyday life

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 10, 2026