search
Back to results

Getting on With the Rest of Your Life After a Stroke

Primary Purpose

Stroke

Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Mission Possible
Sponsored by
McGill University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Stroke

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • living in the community
  • who have completed all formal institution-based, in-patient and ambulatory, rehabilitative interventions.

Exclusion Criteria:

  • already enrolled in existing community based projects
  • persons with cognitive impairment

Sites / Locations

  • Division fo Clinical epidemiology

Arms of the Study

Arm 1

Arm 2

Arm Type

Other

Experimental

Arm Label

Start Later

Start Now

Arm Description

The participants receive the Mission Possible intervention but it is delayed by 3 months.

The participants start the Mission Possible program right away.

Outcomes

Primary Outcome Measures

Participation
participation in leisure measured using the CHAMPS

Secondary Outcome Measures

Full Information

First Posted
March 10, 2010
Last Updated
April 25, 2017
Sponsor
McGill University
Collaborators
Canadian Stroke Network
search

1. Study Identification

Unique Protocol Identification Number
NCT01085240
Brief Title
Getting on With the Rest of Your Life After a Stroke
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
Study Type
Interventional

2. Study Status

Record Verification Date
April 2017
Overall Recruitment Status
Completed
Study Start Date
September 2008 (undefined)
Primary Completion Date
September 2013 (Actual)
Study Completion Date
September 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
McGill University
Collaborators
Canadian Stroke Network

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
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.
Detailed Description
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stroke

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
240 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Start Later
Arm Type
Other
Arm Description
The participants receive the Mission Possible intervention but it is delayed by 3 months.
Arm Title
Start Now
Arm Type
Experimental
Arm Description
The participants start the Mission Possible program right away.
Intervention Type
Other
Intervention Name(s)
Mission Possible
Other Intervention Name(s)
Participation
Intervention Description
The intervention focuses on leisure education, exercise and community re-integration.
Primary Outcome Measure Information:
Title
Participation
Description
participation in leisure measured using the CHAMPS
Time Frame
baseline, 3, 6, 12 and 15 months

10. Eligibility

Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: living in the community who have completed all formal institution-based, in-patient and ambulatory, rehabilitative interventions. Exclusion Criteria: already enrolled in existing community based projects persons with cognitive impairment
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Nancy E Mayo, PhD
Organizational Affiliation
Division of Clinical Epidemiology
Official's Role
Principal Investigator
Facility Information:
Facility Name
Division fo Clinical epidemiology
City
Montreal
State/Province
Quebec
ZIP/Postal Code
H3A 1A1
Country
Canada

12. IPD Sharing Statement

Citations:
PubMed Identifier
34813082
Citation
Crocker TF, Brown L, Lam N, Wray F, Knapp P, Forster A. Information provision for stroke survivors and their carers. Cochrane Database Syst Rev. 2021 Nov 23;11(11):CD001919. doi: 10.1002/14651858.CD001919.pub4.
Results Reference
derived

Learn more about this trial

Getting on With the Rest of Your Life After a Stroke

We'll reach out to this number within 24 hrs