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SMARTease Trial: Evaluating Stroke Help Distance Interventions to Improve Cognitive Performance Post-Stroke (SMARTease)

Primary Purpose

Cognitive Impairment, Stroke

Status
Terminated
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Telerehabilitation Cognitive Strategy Training
Sponsored by
Nova Scotia Health Authority
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cognitive Impairment focused on measuring cognitive rehabilitation, SMART goals, telehealth

Eligibility Criteria

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

Inclusion Criteria:

  • history of one or more strokes;
  • living in the community;
  • subjective concerns about cognitive function;
  • ability to give informed consent;
  • fluent in written and spoken English.

Exclusion Criteria:

  • unstable medical conditions or a co-morbid neurological disorder that could additionally impact cognitive or daily function, such as Parkinson's disease or Multiple Sclerosis;
  • no available caregiver or significant other willing to participate in approximately one hour of telephone contact per week with coach and stroke survivor;
  • current symptoms of severe depression (Geriatric Depression Scale>20), global aphasia, or dementia (determined by baseline testing).

Sites / Locations

  • Capital District Health Authority

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Training

Arm Description

telerehabilitation cognitive strategy training

Outcomes

Primary Outcome Measures

Change in functioning on goal attainment scaling
estimating within subject effect sizes for the treated group based on changes in measures at the level of impairment (self and other-reported cognitive performance), activity (achievement of activity goals and everyday cognitive performance) and participation/quality of life (self-report measures of reintegration to normal living, quality of life, caregiver burden).

Secondary Outcome Measures

Intervention modifiers
Additional secondary analyses will also investigate variables that could modify the effects of the interventions, including cognitive profile, stroke severity and location of lesion, co-morbid conditions, type of functional goal and current environmental factors.
Feasibility of recruitment, retention, compliance
Rates of subject recruitment, retention, and compliance with protocol
Feasibility-Coach adherence
Feasibility of coach adherence to therapy protocols will be assessed weekly through review of adherence to scripts and completeness of data collection

Full Information

First Posted
June 23, 2011
Last Updated
August 29, 2023
Sponsor
Nova Scotia Health Authority
Collaborators
IWK Health Centre, Canadian Institutes of Health Research (CIHR)
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1. Study Identification

Unique Protocol Identification Number
NCT01407081
Brief Title
SMARTease Trial: Evaluating Stroke Help Distance Interventions to Improve Cognitive Performance Post-Stroke
Acronym
SMARTease
Official Title
SMARTease Trial - Turning SMART Goals Into Smart Actions: Evaluating Stroke Help Distance Interventions to Improve Cognitive Performance Post-Stroke
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Terminated
Why Stopped
Poor recruitment
Study Start Date
August 2011 (undefined)
Primary Completion Date
April 2012 (Actual)
Study Completion Date
April 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Nova Scotia Health Authority
Collaborators
IWK Health Centre, Canadian Institutes of Health Research (CIHR)

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to provide evidence for the feasibility and initial effectiveness of a manualized, telephone-based (telehealth) approach to the delivery of cognitive interventions (SMARTease) targeted to improve cognitive performance in daily activities after stroke.
Detailed Description
An initial brief screening interview will be completed with the potential participant by telephone to determine whether or not the individual meets the criteria for the study. In an initial onsite visit, informed consent will be obtained from both the stroke survivor and their study partner and baseline evaluations will be completed with the stroke survivor, including a baseline cognitive assessment and setting goals to work on during the study period. Then the introductory section of the study Handbook (Making the Most of Your Memory) which includes procedural information on the Stroke Help Program will be reviewed with the stroke survivor and study partner. A study Handbook and a large button speaker phone will be provided to the stroke survivor/partner pair to ensure that both members of the participant-caregiver team can listen to the rehabilitation coach without having to be concerned with holding a handset (an action that may be difficult for some stroke survivors). Telephone contact by the rehabilitation coach will be organized and the 16-week Stroke Help Cognitive Strategy Training Intervention will proceed. In general the topics or strategies to be discussed will be used to achieve one or more of the following rehabilitation strategies: 1) Understanding cognitive deficits that may result from stroke; 2). Reinforcing, strengthening or re-establishing previously learned patterns of behavior; 3) Establishing new patterns of compensatory mechanisms; 4) Enabling persons to adapt to their cognitive disability. Following the 16-week Cognitive Strategy Training Intervention participants will have an on-site visit to provide qualitative and quantitative data related to the feasibility and efficacy of the program.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cognitive Impairment, Stroke
Keywords
cognitive rehabilitation, SMART goals, telehealth

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
11 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Training
Arm Type
Experimental
Arm Description
telerehabilitation cognitive strategy training
Intervention Type
Behavioral
Intervention Name(s)
Telerehabilitation Cognitive Strategy Training
Other Intervention Name(s)
cognitive rehabilitation
Intervention Description
The strategy intervention is a 16-week program during which a trained rehabilitation coach speaks by telephone to the stroke participant and their caregiver twice a week (one approximately 45-minute 'training' call and one approximately 15-minute 'update' call). Rehabilitation discussions during the training calls will follow a detailed protocol and focus each week on the stroke education and cognitive strategy training information provided in each section of the manual provided to the participants.
Primary Outcome Measure Information:
Title
Change in functioning on goal attainment scaling
Description
estimating within subject effect sizes for the treated group based on changes in measures at the level of impairment (self and other-reported cognitive performance), activity (achievement of activity goals and everyday cognitive performance) and participation/quality of life (self-report measures of reintegration to normal living, quality of life, caregiver burden).
Time Frame
Measured at baseline and week 18
Secondary Outcome Measure Information:
Title
Intervention modifiers
Description
Additional secondary analyses will also investigate variables that could modify the effects of the interventions, including cognitive profile, stroke severity and location of lesion, co-morbid conditions, type of functional goal and current environmental factors.
Time Frame
measured at baseline and weekly until end of study at week 18
Title
Feasibility of recruitment, retention, compliance
Description
Rates of subject recruitment, retention, and compliance with protocol
Time Frame
measured at end of 16 week study
Title
Feasibility-Coach adherence
Description
Feasibility of coach adherence to therapy protocols will be assessed weekly through review of adherence to scripts and completeness of data collection
Time Frame
measured at weekly intervals

10. Eligibility

Sex
All
Minimum Age & Unit of Time
19 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: history of one or more strokes; living in the community; subjective concerns about cognitive function; ability to give informed consent; fluent in written and spoken English. Exclusion Criteria: unstable medical conditions or a co-morbid neurological disorder that could additionally impact cognitive or daily function, such as Parkinson's disease or Multiple Sclerosis; no available caregiver or significant other willing to participate in approximately one hour of telephone contact per week with coach and stroke survivor; current symptoms of severe depression (Geriatric Depression Scale>20), global aphasia, or dementia (determined by baseline testing).
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Gail A Eskes, Ph.D.
Organizational Affiliation
Capital District Health Authority, Nova Scotia, Canada
Official's Role
Principal Investigator
Facility Information:
Facility Name
Capital District Health Authority
City
Halifax
State/Province
Nova Scotia
ZIP/Postal Code
B3H 1V7
Country
Canada

12. IPD Sharing Statement

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SMARTease Trial: Evaluating Stroke Help Distance Interventions to Improve Cognitive Performance Post-Stroke

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