With an aging population, and survival rates now at 83% in Canada, the number of stroke
survivors is expected to reach 720,000 by 2038. While 90% of individuals with stroke return
to independent community living, 80% report residual motor impairment, such as loss or
limitation in motor control, or mobility limitation. These limitations have profound effects
on the ability to perform everyday activities and are associated with substantial economic
strain on the healthcare system. Thus, a primary focus of stroke rehabilitation is on the
recovery of motor function, walking and balance, using exercise via physical therapy.
The rapid growth in Internet use and personal mobile devices has opened an array of
possibilities for stroke survivors to remotely access specialized rehabilitation from their
homes and communities (i.e., telerehabilitation). Telerehabilitation interventions have been
used effectively for check-in sessions, education, and counselling after stroke, but
knowledge of the effectiveness of using telerehabilitation for the delivery of exercise
interventions for lower extremity recovery is limited.
The investigators developed the TeleRehabilitation with Aims to Improve Lower Extremity
Recovery Post-Stroke (TRAIL) to address the unmet needs for lower extremity rehabilitation
after stroke, and the need for accessible rehabilitation in the face of the COVID-19
pandemic. TRAIL is an exercise program designed to promote lower extremity recovery using
technology with real-time therapist instruction and guidance. The investigators recently
conducted a proof-of-concept, single-group feasibility study of TRAIL (TRAIL-PROOF). From
TRAIL-PROOF, there were have no reports of serious adverse events and 100% retention of
participants. Preliminary analysis of 32 individuals completed also suggest improvements in
the clinical outcomes, including increased lower extremity strength, functional balance, and
balance self-efficacy. Thus, from TRAIL-PROOF, it is evident that the TRAIL protocol has
potential to improve lower extremity function among community-dwelling adults with stroke
experiencing lower extremity impairment. The investigators now propose a full-scaled
randomized controlled trial to further study the TRAIL program (TRAIL-RCT).
The objectives for TRAIL-RCT are as follows:
The primary objective is to compare functional mobility (Timed Up and Go, primary
clinical outcome) after 4 weeks of TRAIL to a 4-week attention-controlled education
program (EDUCATION) in individuals ≤12 months post-stroke;
The secondary objective is to compare the 4-week TRAIL and EDUCATION programs on
secondary outcomes of:
Lower extremity strength (30-Second Sit-to Stand test);
Functional balance (Tandem Stand and Functional Reach);
Motor impairment (Virtual Fugl-Meyer Assessment);
Balance self-efficacy (Activities-specific Balance Confidence Scale);
The tertiary objective is to compare the 4-week TRAIL and EDUCATION programs on health
economic outcomes:
Health-related quality of life (Stroke Impact Scale, EuroQol-5D-5 Level); and
Health resources and costs (Health Resource Utilization Questionnaire)
The quaternary objective is to evaluate the feasibility of a subsequent larger multisite
implementation stepped wedge randomized trial of TRAIL using pre-specified criteria
related to process, resources, management, and scientific indicators.
It is hypothesized that:
The primary hypothesis is that the 4-week TRAIL program will lead to greater improvement in
functional mobility, as measured by the Timed Up and Go, compared to the 4-week EDUCATION
program in individuals ≤12 months post-stroke (Objective 1, primary clinical outcome).
The investigators also anticipate that greater improvements will be observed in the secondary
clinical outcomes, in the areas of lower extremity muscle strength, motor impairment,
functional balance, and balance self-efficacy, following TRAIL compared to EDUCATION
(Objective 2).
The tertiary hypothesis is that the TRAIL intervention will demonstrate superior health
economic outcomes compared to the EDUCATION group (Objective 3).
The quaternary hypothesis is that the protocol will demonstrate sufficient feasibility (e.g.,
rates of recruitment/retention, treatment fidelity and adherence, safety, treatment effects)
to support a subsequent larger multi-site implementation stepped wedge randomized controlled
trial (Objective 4).