Effectiveness of Computer-based Cognitive Training for Executive Functions After Stroke
Primary Purpose
Stroke, Executive Dysfunction, Cognitive Impairment
Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
CogniPlus
Training As Usual (TAU)
Sponsored by

About this trial
This is an interventional treatment trial for Stroke
Eligibility Criteria
Inclusion Criteria:
- Patients are suffered from unilateral hemispheric stroke and with a confirmation by neuroimaging evidence from either computer tomography (CT) or magnetic resonance imaging (MRI);
- Patients are either at subacute stage or chronic stage, i.e. the patients are suffered from post-stroke after one month,
- Patients are age 60 years old or above;
- Patients are medically stable;
- Patients are Cantonese speaking,
- Patients can communicate and to follow at least three-step commands, and;
- Patients are willing to give written consent.
Exclusion Criteria:
- Patients are at acute stage, i.e the patients are suffered from stroke within 1 week;
- Patients with severe aphasia, swallowing disorders or other complications post-stroke that prevent them from successfully completing the assessments;
- Patients with any previously known psychiatric disorder or neurological disease excluding stroke;
- Patients are unable to given written consent.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Experimental CBCT Group
Training As Usual (TAU) Group
Arm Description
Participants of CBCT group will attend individual computer-based cognitive training sessions. Researcher will give instruction in the use of the computerized training programs and assists participants during their training sessions.
Participants of TAU group will attend usual training sessions offered by the training centres with similar intensity and frequency as the CBCT training.
Outcomes
Primary Outcome Measures
Change of Wisconsin Card Sorting Test Score
The test consists of 128 card designs, participant is required to sort the cards under the categorization rules and feedback from examiner in about 20 minutes. The more categories achieved (range 0 to 6) and less perseverative errors (out of 128 trials) the better executive control. Moreover, the lower the total number of trials administered (total number of cards used) reflects greater efficiency of the participant in the task; in addition, the greater the total number of correct responses (number of successes in combinations according to the category) and the lower the total number of errors (number of incorrect combinations) also indicate the better the participant's performance.
Secondary Outcome Measures
Full Information
NCT ID
NCT04944004
First Posted
June 22, 2021
Last Updated
June 28, 2021
Sponsor
TWGHs Wong Tai Sin Hospital
Collaborators
The Hong Kong Polytechnic University
1. Study Identification
Unique Protocol Identification Number
NCT04944004
Brief Title
Effectiveness of Computer-based Cognitive Training for Executive Functions After Stroke
Official Title
Effectiveness of Computer-based Cognitive Training for Executive Functions After Stroke
Study Type
Interventional
2. Study Status
Record Verification Date
June 2021
Overall Recruitment Status
Unknown status
Study Start Date
July 1, 2021 (Anticipated)
Primary Completion Date
July 1, 2022 (Anticipated)
Study Completion Date
October 31, 2022 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
TWGHs Wong Tai Sin Hospital
Collaborators
The Hong Kong Polytechnic University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Objective:
To determine the efficacy of computer-based cognitive training(CBCT) in patients with stroke in the community settings.
Study Design:
Single-blinded prospective, pre-test/post-test randomized controlled trial (RCT) will be conducted in 2 groups of participants that receiving training in community settings. Treatment groups will attend individualized CBCT programme using CogniPlus® while control group will continue attend conventional treatment as usual (TAU). Assessment on the means difference in assessing functions will be done after the study.
Samples:
100 patients with stroke will be recruited from the community, using a sampling frame of selected diagnosis and homogeneity.
Expected Findings:
Find out the training effects of selected CBCT on EF and daily functioning in patients with stroke
Detailed Description
It is important to study the effectiveness of intervention post-stroke cognitive deficits in EF, Post-stroke patients with EF deficits will affect their abilities to successfully return to normal daily activity. Studies over the past decade have provided evidence of substantial gaps in our knowledge on how to effectively manage EF impairment post-stroke. To address these gaps there has been growing attention and research into the management of EF impairment post-stroke. Studies have been conducted to address some of these gaps specific to EF impairment and intervention research, and to investigate use of evidence-based practices for the management of EF impairment post-stroke. The literatures review of EF interventions identified different treatment approaches that were showing promise in helping persons with stroke to cope with EF deficits. The preliminary evidence on specific EF skill retraining suggested that structured, individualized, and intense computerized EF training could improve targeted EF impairments. Stroke patients with EF deficits often find it difficult in their daily activities, the impact of treatment might have potential to enhance rehabilitation and recovery. The translational framework described in (figure IV) describe ways to identify and investigate the evidence for the use of CBCT in specific EF interventions post-stroke. The study is thus required to find the impact of CBCT on a variety of outcomes, including not only measures of EF impairment, but also measures of daily activities and participation in everyday life situations that are affected in stroke patients having EF disorders.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stroke, Executive Dysfunction, Cognitive Impairment, Randomized Controlled Trial
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Masking Description
Single blinded
Allocation
Randomized
Enrollment
100 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Experimental CBCT Group
Arm Type
Experimental
Arm Description
Participants of CBCT group will attend individual computer-based cognitive training sessions. Researcher will give instruction in the use of the computerized training programs and assists participants during their training sessions.
Arm Title
Training As Usual (TAU) Group
Arm Type
Active Comparator
Arm Description
Participants of TAU group will attend usual training sessions offered by the training centres with similar intensity and frequency as the CBCT training.
Intervention Type
Other
Intervention Name(s)
CogniPlus
Intervention Description
The CBCT programmes proposed in this study is called CogniPlus. This software package offers training of scientifically proven trainable cognitive functions. According to the user manual, the lifelike interactive system and its automatic adaptability to client's ability level made CogniPlus feasible in community settings.
Intervention Type
Other
Intervention Name(s)
Training As Usual (TAU)
Intervention Description
Training As Usual (TAU)
Primary Outcome Measure Information:
Title
Change of Wisconsin Card Sorting Test Score
Description
The test consists of 128 card designs, participant is required to sort the cards under the categorization rules and feedback from examiner in about 20 minutes. The more categories achieved (range 0 to 6) and less perseverative errors (out of 128 trials) the better executive control. Moreover, the lower the total number of trials administered (total number of cards used) reflects greater efficiency of the participant in the task; in addition, the greater the total number of correct responses (number of successes in combinations according to the category) and the lower the total number of errors (number of incorrect combinations) also indicate the better the participant's performance.
Time Frame
Baseline, after completion of half of the programme (an average of 8 weeks), one month post-treatment
10. Eligibility
Sex
All
Minimum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients are suffered from unilateral hemispheric stroke and with a confirmation by neuroimaging evidence from either computer tomography (CT) or magnetic resonance imaging (MRI);
Patients are either at subacute stage or chronic stage, i.e. the patients are suffered from post-stroke after one month,
Patients are age 60 years old or above;
Patients are medically stable;
Patients are Cantonese speaking,
Patients can communicate and to follow at least three-step commands, and;
Patients are willing to give written consent.
Exclusion Criteria:
Patients are at acute stage, i.e the patients are suffered from stroke within 1 week;
Patients with severe aphasia, swallowing disorders or other complications post-stroke that prevent them from successfully completing the assessments;
Patients with any previously known psychiatric disorder or neurological disease excluding stroke;
Patients are unable to given written consent.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Ray Li, MSc
Phone
852 98312636
Email
rayliot@yahoo.com.hk
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Effectiveness of Computer-based Cognitive Training for Executive Functions After Stroke
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