Stroke Canada Optimization of Rehabilitation by Evidence Implementation Trial SCORE-IT)
Recruitment status was Recruiting
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Purpose
The aim of this project is to evaluate whether using an implementation intervention promotes use of best practices by rehabilitation professionals and leads to improvements in patient outcomes for individuals with stroke.
| Condition | Intervention | Phase |
|---|---|---|
|
Stroke |
Behavioral: Knowledge translation intervention package |
Phase 2 Phase 3 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Parallel Assignment Masking: Single Blind |
| Official Title: | Stroke Canada Optimization of Rehabilitation by Evidence Implementation Trial (SCORE IT) |
- Arm function as measured by the Box and Block test
- Walking speed as measured by the 6 minutes walk test
- Arm function as measured by the Chedoke Arm and Hand Activity Inventory (CAHAI- 9)
- Impairment as measured by the Chedoke-McMaster Stroke Assessment Scale (CMSA)
- Independence of daily living as measured by the 3. Functional Independence Measure (FIM)
- Economic outcomes measured by the Quality Adjusted Life Years (QALY)
| Estimated Enrollment: | 2000 |
| Study Start Date: | September 2006 |
| Estimated Study Completion Date: | April 2008 |
Stroke is a leading cause of disability in Canada and frequently causes hemiparesis (upper limb and lower limb weakness on one side of the body). Approximately one third of stroke survivors require physical rehabilitation to improve their motor and functional recovery (1). Although many strategies have been shown to be effective in promoting recovery after stroke, the uptake of evidence-based practice by rehabilitation professionals across Canada is variable. The aim of this project is to evaluate whether using an implementation intervention promotes use of best practices by rehabilitation professionals and leads to improvements in patient outcomes for individuals with stroke.
This project is a cluster randomized implementation trial for upper and lower limb interventions. Rehabilitation centres across Canada will be randomized to receive either an outcome-oriented implementation strategy (OOI) to facilitate implementation of the EIPRs or a process-oriented implementation strategy (POI). At the onset, rehabilitation professionals practicing in all centres will receive education in using best practice outcome measures related to stroke rehabilitation. All centres will be assessed for baseline adherence to the EIPRs. Centres in the OOI will receive "usual care" (i.e. passive dissemination of the written protocols and information about outcome measures). Centres in the POI arm will receive a combination of strategies to facilitate EIPR uptake (i.e., use of a local facilitator, practice audits with feedback, reminder systems and educational sessions). Following exposure to the EIPRs, all centres will document adherence to the EIPRs, and patient outcomes as assessed by the measures. An analysis of the costs associated with rehabilitation interventions and the incremental expense of a POI strategy will be undertaken. These data will be used to compare the OOI and POI centres with respect to the level of uptake and implementation of EIPRs and related expenses.
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Rehabilitation Hospitals/Research Sites:
Inclusion Criteria:
- hospital with designated rehabilitation beds;
- regularly treats stroke patients;
- has access to at least one physical (PT) and one occupational (OT) therapist on the health professional team
Exclusion Criteria:
- Inadequate staffing to administer the outcome measures consistently
Patients:
Inclusion Criteria:
- medically stable;
- stroke with residual disability;
- requires complex rehabilitation interventions from at least 3 health care professionals, one of them being an OT or a PT;
- admitted to rehabilitation centre within 90 days of stroke onset;
- and age >18 years
Exclusion Criteria:
- having a medical condition that is expected to result in death within 6 months;
- presence of a serious chronic disabling condition that impacts on either the rehabilitation process or rehabilitation outcomes such as severe arthritis, dementia, Parkinson's disease;
- active suicidal ideation or symptoms of psychosis
Contacts and Locations| Contact: Amanda G Hurdowar, MSc | 416-597-3422 ext 7859 | Hurdowar.Amanda@TorontoRehab.on.ca |
| Canada, Ontario | |
| Toronto Rehabilitation Institute | Recruiting |
| Toronto, Ontario, Canada, M5G 2A2 | |
| Contact: Amanda Hurdowar, MSc 416-597-3422 ext 7859 Hurdowar.Amanda@TorontoRehab.on.ca | |
| Principal Investigator: Mark T Bayley, MD | |
| Canada, Quebec | |
| McGill University | Not yet recruiting |
| Montreal, Quebec, Canada, H3G 1Y5 | |
| Contact: Sharon Wood-Dauphinee, PhD (514) 398-5326 sharon.wood.dauphinee@mcgill.ca | |
| Principal Investigator: Sharon Wood-Dauphinee, PhD | |
| Principal Investigator: | Mark T Bayley, MD | Toronto Rehabilitation Institute |
| Principal Investigator: | Sharon Wood-Dauphinee, PhD | McGill University |
More Information
No publications provided
| ClinicalTrials.gov Identifier: | NCT00359593 History of Changes |
| Other Study ID Numbers: | CSNscore |
| Study First Received: | July 31, 2006 |
| Last Updated: | March 19, 2008 |
| Health Authority: | Canada: Health Canada |
Keywords provided by Toronto Rehabilitation Institute:
|
Stroke Rehabilitation Knowledge translation Evidence based practice Outcomes |
Additional relevant MeSH terms:
|
Stroke Cerebral Infarction Cerebrovascular Disorders Brain Diseases Central Nervous System Diseases |
Nervous System Diseases Vascular Diseases Cardiovascular Diseases Brain Infarction Brain Ischemia |
ClinicalTrials.gov processed this record on May 19, 2013