Stroke Clinical Trial
Official title:
Effectiveness of Computer-based Cognitive Training for Executive Functions After Stroke
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
Status | Not yet recruiting |
Enrollment | 100 |
Est. completion date | October 31, 2022 |
Est. primary completion date | July 1, 2022 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 60 Years and older |
Eligibility | Inclusion Criteria: 1. Patients are suffered from unilateral hemispheric stroke and with a confirmation by neuroimaging evidence from either computer tomography (CT) or magnetic resonance imaging (MRI); 2. Patients are either at subacute stage or chronic stage, i.e. the patients are suffered from post-stroke after one month, 3. Patients are age 60 years old or above; 4. Patients are medically stable; 5. Patients are Cantonese speaking, 6. Patients can communicate and to follow at least three-step commands, and; 7. Patients are willing to give written consent. Exclusion Criteria: 1. Patients are at acute stage, i.e the patients are suffered from stroke within 1 week; 2. Patients with severe aphasia, swallowing disorders or other complications post-stroke that prevent them from successfully completing the assessments; 3. Patients with any previously known psychiatric disorder or neurological disease excluding stroke; 4. Patients are unable to given written consent. |
Country | Name | City | State |
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n/a |
Lead Sponsor | Collaborator |
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TWGHs Wong Tai Sin Hospital | The Hong Kong Polytechnic University |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | 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. | Baseline, after completion of half of the programme (an average of 8 weeks), one month post-treatment |
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