- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05367128
Effects of Dual Task Prioritization Training on Dual Task Walking in Older People
Effects of Dual Task Prioritization Training on Dual Task Walking in Older People: A Single-blinded Randomized Controlled Trial
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Introduction: Many activities of daily livings involve performing two tasks simultaneously, i.e. dual tasking. Performing dual task increases the demand on attentional resources, which may further decrease the dual task performance, especially in older adults. According to capacity sharing theory, the two tasks compete and influence with each other due to limited attention and information processing capacity. It has been noted that task prioritization during dual tasking may influence the dual task performance. Previous study indicated that supraposture-focus strategy resulted in better posture and task performance in older people. On the other hand, it is known that dual task training improved dual task performance. However, the effects of applying task prioritization during dual task training have not yet been investigated. Therefore, the purpose of this study is to investigate the effect of different task prioritization during dual task training on dual task performance.
Methods: Participants will be randomized into three groups: posture-focus, supraposture-focus and control group. Participants will receive a total of 12 sessions of cognitive dual task training with different prioritization strategies, i.e. prioritization on posture, cognitive or neither task. Walking and task performance during dual task walking, executive function, and balance performance will be assessed before and after the interventions (pre- and post-test).
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Ray-Yau Wang, PhD
- Phone Number: +886-2-2826-7210
- Email: rywang@nycu.edu.tw
Study Locations
-
-
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Taipei, Taiwan, 112
- Recruiting
- National Yang Ming Chiao Tung University
-
Contact:
- Ray-Yau Wang, PhD
- Phone Number: +886-2-28267210
- Email: rywang@nycu.edu.tw
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Age ≥ 65 years old
- MMSE scores > 24
Exclusion Criteria:
- Unstable health conditions
- Any neurological, psychological disease or diagnosis of learning disability which interferes the participation in this study
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Posture-focus group
Participants will be instructed to pay most attention to practice the posture task during training
|
All participants will receive cognitive dual task training for 30 min/session, 2-3 sessions/week for 4-6 weeks (a total of 12 sessions).
The cognitive dual task training includes 15 min of cognitive task combining with standing task and 15 min of cognitive task combining with walking task.
The differences among group are the instructions of task prioritization given by the therapist
|
Experimental: Supraposture-focus group
Participants will be instructed to pay most attention to practice the cognitive task during training
|
All participants will receive cognitive dual task training for 30 min/session, 2-3 sessions/week for 4-6 weeks (a total of 12 sessions).
The cognitive dual task training includes 15 min of cognitive task combining with standing task and 15 min of cognitive task combining with walking task.
The differences among group are the instructions of task prioritization given by the therapist
|
Active Comparator: Control group
Participants will not be receive any instruction to prioritize either task
|
All participants will receive cognitive dual task training for 30 min/session, 2-3 sessions/week for 4-6 weeks (a total of 12 sessions).
The cognitive dual task training includes 15 min of cognitive task combining with standing task and 15 min of cognitive task combining with walking task.
The differences among group are the instructions of task prioritization given by the therapist
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Dual task walking performance assessment- speed (m/s)
Time Frame: Change from baseline dual task walking speed and up to 6 weeks (pre- and post-test)
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Using GaitUp system to evaluate gait speed during cognitive and motor dual task walking
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Change from baseline dual task walking speed and up to 6 weeks (pre- and post-test)
|
Dual task walking performance assessment- cadence (steps/min)
Time Frame: Change from baseline dual task walking cadence and up to 6 weeks (pre- and post-test)
|
Using GaitUp system to evaluate cadence during cognitive and motor dual task walking
|
Change from baseline dual task walking cadence and up to 6 weeks (pre- and post-test)
|
Dual task walking performance assessment- stride length variability (CV, %)
Time Frame: Change from baseline dual task walking stride length variability and up to 6 weeks (pre- and post-test)
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Using GaitUp system to evaluate stride length variability during cognitive and motor dual task walking
|
Change from baseline dual task walking stride length variability and up to 6 weeks (pre- and post-test)
|
Dual task walking performance assessment- stride time variability (CV, %)
Time Frame: Change from baseline dual task walking stride time variability and up to 6 weeks (pre- and post-test)
|
Using GaitUp system to evaluate stride time variability during cognitive and motor dual task walking
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Change from baseline dual task walking stride time variability and up to 6 weeks (pre- and post-test)
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Rate of dual task cost- gait speed (%)
Time Frame: Change from baseline dual task cost and up to 6 weeks (pre- and post-test)
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Using the dual and single task walking speed to calculate the dual task cost of gait speed
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Change from baseline dual task cost and up to 6 weeks (pre- and post-test)
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Trail Making Test
Time Frame: Change from baseline Trail Making Test and up to 6 weeks (pre- and post-test)
|
Use Trail Making Test (TMT)-Chinese version to indicate executive function.
The duration for completing the test will be measured, and the shorter duration means the better executive function.
|
Change from baseline Trail Making Test and up to 6 weeks (pre- and post-test)
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Berg Balance Scale
Time Frame: Change from baseline Berg Balance Scale and up to 6 weeks (pre- and post-test)
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Use Berg Balance Scale (BBS) to assess balance performance.
Berg balance scale scoring ranges from 0 to 56.
The higher scores indicate better balance performance.
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Change from baseline Berg Balance Scale and up to 6 weeks (pre- and post-test)
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Single task walking performance assessment- speed (m/s)
Time Frame: Change from baseline single task walking speed and up to 6 weeks (pre- and post-test)
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Using GaitUp system to evaluate gait speed during single walking
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Change from baseline single task walking speed and up to 6 weeks (pre- and post-test)
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Single task walking performance assessment- cadence (steps/min)
Time Frame: Change from baseline single task walking cadence and up to 6 weeks (pre- and post-test)
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Using GaitUp system to evaluate cadence during single walking
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Change from baseline single task walking cadence and up to 6 weeks (pre- and post-test)
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Single task walking performance assessment- stride length variability (CV, %)
Time Frame: Change from baseline single task walking stride length variability and up to 6 weeks (pre- and post-test)
|
Using GaitUp system to evaluate stride length variability during single walking
|
Change from baseline single task walking stride length variability and up to 6 weeks (pre- and post-test)
|
Single task walking performance assessment- stride time variability (CV, %)
Time Frame: Change from baseline dual task walking stride time variability and up to 6 weeks (pre- and post-test)
|
Using GaitUp system to evaluate stride time variability during single walking
|
Change from baseline dual task walking stride time variability and up to 6 weeks (pre- and post-test)
|
Cognitive dual task walking performance assessment- correct number (times)
Time Frame: Change from baseline cognitive dual task walking performance and up to 6 weeks (pre- and post-test)
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The number of the correct answer for serially subtracting "7" from a predefined 3-digit number during cognitive dual task walking task will be recorded.
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Change from baseline cognitive dual task walking performance and up to 6 weeks (pre- and post-test)
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Motor dual task walking performance assessment- number of go (pieces)
Time Frame: Change from baseline motor dual task walking performance and up to 6 weeks (pre- and post-test)
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The number of successfully transferred go pieces from one side to another during motor dual task walking task will be recorded.
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Change from baseline motor dual task walking performance and up to 6 weeks (pre- and post-test)
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Ray-Yau Wang, PhD, National Yang Ming Chiao Tung University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
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
Other Study ID Numbers
- YM111015F
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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