NCT00359593

Brief 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.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
2,000

participants targeted

Target at P75+ for phase_2 stroke

Timeline
Completed

Started Sep 2006

Shorter than P25 for phase_2 stroke

Geographic Reach
1 country

2 active sites

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

July 31, 2006

Completed
2 days until next milestone

First Posted

Study publicly available on registry

August 2, 2006

Completed
1 month until next milestone

Study Start

First participant enrolled

September 1, 2006

Completed
1.6 years until next milestone

Study Completion

Last participant's last visit for all outcomes

April 1, 2008

Completed
Last Updated

March 20, 2008

Status Verified

July 1, 2006

First QC Date

July 31, 2006

Last Update Submit

March 19, 2008

Conditions

Keywords

StrokeRehabilitationKnowledge translationEvidence based practiceOutcomes

Outcome Measures

Primary Outcomes (2)

  • Arm function as measured by the Box and Block test

  • Walking speed as measured by the 6 minutes walk test

Secondary Outcomes (4)

  • 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)

Interventions

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • 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

You may not qualify if:

  • Inadequate staffing to administer the outcome measures consistently
  • Patients:
  • 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
  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (2)

Toronto Rehabilitation Institute

Toronto, Ontario, M5G 2A2, Canada

RECRUITING

McGill University

Montreal, Quebec, H3G 1Y5, Canada

NOT YET RECRUITING

Related Publications (1)

  • 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.

Related Links

MeSH Terms

Conditions

Stroke

Condition Hierarchy (Ancestors)

Cerebrovascular DisordersBrain DiseasesCentral Nervous System DiseasesNervous System DiseasesVascular DiseasesCardiovascular Diseases

Study Officials

  • Mark T Bayley, MD

    Toronto Rehabilitation Institute

    PRINCIPAL INVESTIGATOR
  • Sharon Wood-Dauphinee, PhD

    McGill University

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Study Design

Study Type
interventional
Phase
phase 2
Allocation
RANDOMIZED
Masking
SINGLE
Intervention Model
PARALLEL
Sponsor Type
OTHER

Study Record Dates

First Submitted

July 31, 2006

First Posted

August 2, 2006

Study Start

September 1, 2006

Study Completion

April 1, 2008

Last Updated

March 20, 2008

Record last verified: 2006-07

Locations