CClinicalTrials.gg
Status unknownNCT00359593Updated Mar 20, 2008

Stroke Canada Optimization of Rehabilitation by Evidence Implementation Trial SCORE-IT)

A Phase 2/3 interventional study of Knowledge translation intervention package in Stroke, sponsored by Toronto Rehabilitation Institute. Status unknown at 2 sites in Canada. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2008-03-20.

Sponsored by Toronto Rehabilitation Institute · Phase 2/3 and Interventional

The sponsor has not verified this record recently (last verified Jul 2006), so the status shown — last known as Recruiting — may be out of date.
Phase
Phase 2/3
Study type
Interventional
Enrollment
2,000
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

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.

Read the detailed description

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.

02

Conditions studied

  • Stroke

Browse trials for

Keywords

  • Stroke
  • Rehabilitation
  • Knowledge translation
  • Evidence based practice
  • Outcomes
03

In context

Stroke

7,286 studies on the registry are indexed under Stroke; 2,013 are open to participants now.

This study's planned enrollment of 2,000 is above the median of 50 across 5,366 interventional studies indexed under Stroke.

Browse Stroke studies →

Lead sponsor

Toronto Rehabilitation Institute is the lead sponsor of 39 studies on the registry; 5 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Eligibility criteria

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
05

Study design

Phase
Phase 2 / Phase 3
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single
Enrollment
2,000 participants (estimated)

Interventions

  • BehavioralKnowledge translation intervention package
06

What researchers measure

Primary outcomes

  1. Arm function as measured by the Box and Block test

  2. Walking speed as measured by the 6 minutes walk test

Secondary outcomes

  1. Arm function as measured by the Chedoke Arm and Hand Activity Inventory (CAHAI- 9)

  2. Impairment as measured by the Chedoke-McMaster Stroke Assessment Scale (CMSA)

  3. Independence of daily living as measured by the 3. Functional Independence Measure (FIM)

  4. Economic outcomes measured by the Quality Adjusted Life Years (QALY)

07

Study locations

1 of 2 sites recruiting
  • Toronto Rehabilitation Institute
    Toronto, Ontario M5G 2A2, Canada
    Recruiting
  • McGill University
    Montreal, Quebec H3G 1Y5, Canada
    Not yet recruiting
08

References and documents

Publications

  • Salbach NM, Wood-Dauphinee S, Desrosiers J, Eng JJ, Graham ID, Jaglal SB, Korner-Bitensky N, MacKay-Lyons M, Mayo NE, Richards CL, Teasell RW, Zwarenstein M, Bayley MT; Stroke Canada Optimization of Rehabilitation By Evidence - Implementation Trial (SCORE-IT) Team. Facilitated interprofessional implementation of a physical rehabilitation guideline for stroke in inpatient settings: process evaluation of a cluster randomized trial. Implement Sci. 2017 Aug 1;12(1):100. doi: 10.1186/s13012-017-0631-7. PubMed 28764752 ↗
09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 20, 2008, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT00359593
Lead sponsor
Toronto Rehabilitation Institute
Collaborators
McGill University
First posted
Aug 2, 2006
Start date
Sep 2006
Completion
Apr 2008 (estimated)
Last update
Mar 20, 2008

Study contacts

Amanda G Hurdowar, MSc
Contact
Hurdowar.Amanda@TorontoRehab.on.ca
416-597-3422 ext. 7859
Mark T Bayley, MD
principal investigator · Toronto Rehabilitation Institute
Sharon Wood-Dauphinee, PhD
principal investigator · McGill University
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Jul 2006. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion