Stroke Clinical Trial
Official title:
Getting on With the Rest of Your Life After Stroke: A Cross-Canada Program Aimed at Enhanced Life Participation, Prevention of Deterioration and Optimization of Health Care Utilization
The primary objective is to determine the extent to which participation in life's roles can
be optimized through the provision of a community-based structured program providing the
opportunity for physical activity, leisure, and social interaction.
A secondary objective is to estimate the extent to which participation is associated with
health benefits including health-related quality of life and reduction of unplanned
health-care encounters for the person with stroke and reduction of burden and improvement in
quality of life for caregivers.
In the fall of 2004, a group of rehabilitation researchers developed a protocol for a
cross-Canada randomized trial aimed at enhancing life participation after stroke. This
project was an important part of the CSN's program and its renewal submission to the
Networks of Centers of Excellence. In December 2004 the Canadian Stroke Network agreed to
fund pilot work for this ambitious project, spread over six sites. The pilot funding
permitted key aspects of the protocol to be developed and put in place: (i) elements of the
intervention have been chosen (physical activity, leisure and social) (ii) the assessment
tools have been chosen and tested; (iii) community-based partner organizations have been
identified; and (iv) the intervention prototype has been tested for feasibility.
The primary objective of the main trial is to determine the extent to which participation in
life's roles can be optimized through the provision of a community-based structured program
providing the opportunity for physical activity, leisure, and social interaction. A
secondary objective is to estimate the extent to which participation is associated with
health benefits including health-related quality of life and reduction of unplanned
health-care encounters for the person with stroke and reduction of burden and improvement in
quality of life for caregivers. In this context, the meaning of "participation" is as
defined by the World' Health Organization (WHO) and reflects both society's and the person's
perspective.
The target population will be persons living in the community who have completed all formal
institution-based, in-patient and ambulatory, rehabilitative interventions. No restriction
on time since stroke will be imposed. Excluded will be persons who are already enrolled in
existing community based projects and persons with cognitive impairment.
Sites: Six sites participated in the feasibility phase. Information emanating from these
sites as well as dissemination activities of the CSN and the Canadian Stroke Strategy, have
led to interest expressed by other sites across Canada prepared to run the trial phase of
this project.
The study design proposed is a two-period, site-stratified, randomized, crossover design
with timing of entry randomized to immediate entry or delayed entry so that there is about a
six month time difference between groups. The intervention period is 9 months and the
follow-up period is an additional 6 months (total 15 mos.) This design would provide for
both assessment of between- group and within-person change. The main outcome is the amount
of time spent in meaningful activity during the day (outcome related to primary objective).
Sample size required to have sufficient power to detect between-group differences is 240
subjects from sites across Canada. As there is considerable interest in community
reintegration, "snowball" entry of sites would make it more realistic to accumulate sample
size and would also make the results more generalizable and locally responsive.
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