- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06413732
The Effect of Dual Task Training in Patients With Stroke
The Effect of Dual Task Training on Gait, Balance, and Quality of Life in Patients With Stroke
Study Overview
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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-
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Karabuk, Turkey, 78050
- Tarik Ozmen
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Having a score of 24 or above on the Mini-Mental State Test,
- Being able to walk at least 10 meters without using a walking aid
- Having a total score of 5 on the motor and cognitive sections of the Functional Independence Scale.
Exclusion Criteria:
- Neurological and orthopedic problems that could affect motor performance and balance
- Communication problems
- Patients who had received Botulinum Toxin injection treatment in the last six months
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Group I
The dual-task training program combined with conventional physiotherapy was applied to both groups for approximately 1 hour, 5 days a week.
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Conventional physiotherapy was applied for approximately 1 hour, 5 days a week.
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Other: Group II
Only conventional physiotherapy was applied to both groups for approximately 1 hour, 5 days a week.
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Conventional physiotherapy was applied for approximately 1 hour, 5 days a week.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Berg Balance Scale
Time Frame: Six weeks
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It is a scale designed to evaluate balance and determine the risk of falling.
It consists of 14 items based on performance of sitting, standing, and posture change.
Scores can range from 0 to 56.
The higher the score, the better the postural control.
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Six weeks
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Timed Up and Go Test
Time Frame: Six weeks
|
The participant was asked to get up from the chair he was sitting on, walk 3 meters at a safe and normal speed, and then turn back and sit on the chair again.
The time was recorded by a stopwatch.
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Six weeks
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10-meter walk test
Time Frame: Six weeks
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The 10-meter walk test (10MWT) is suggested for assessing gait in post-stroke rehabilitation.
The participant was instructed to walk at comfortable walking speed a distance of 10 meters.
The time was recorded in seconds with a stopwatch.
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Six weeks
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30-Second Chair-Stand Test
Time Frame: Six weeks
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For this test, the participant was seated on a chair with a sitting height of 45-47 cm, with his arms on his chest, and was asked to stand up and sit down as many times as possible within 30 seconds.
The score was recorded as zero if the participant could not get up from the chair without using their arms
|
Six weeks
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Short Form 36
Time Frame: Six weeks
|
The scale consists of 36 items in the following categories: physical function, social function, physical role, emotional role, mental health, vitality, bodily pain, and general health. Subscales evaluate health between 0 and 100, with 0 indicating poor health and 100 indicating good health. The scale consists of 36 items in the following categories: physical function, social function, physical role, emotional role, mental health, vitality, bodily pain, and general health. Subscales evaluate health between 0 and 100, with 0 indicating poor health and 100 indicating good health. The scale consists of 36 items in the following categories: physical function, social function, physical role, emotional role, mental health, vitality, bodily pain, and general health. Subscales evaluate health between 0 and 100, with 0 indicating poor health and 100 indicating good health. |
Six weeks
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Karabuk Physiotherapy
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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