- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06794177
The Effects of Dual Task Training With Different Task Priorities on Physical Performance and Cognitive Status in Patients With Parkinson's Disease
October 2, 2025 updated by: Elvan ÖZCAN GÜLŞEN, Hacettepe University
Investigation of the Effects of Dual Task Training With Different Task Priorities on Physical Performance and Cognitive Status in Patients With Parkinson's Disease
This study was planned to investigate and compare the effects of variable and fixed priority dual task training on balance, walking skills, mobility and cognition in patients with Parkinson's disease.
Study Overview
Status
Completed
Study Type
Interventional
Enrollment (Actual)
30
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Ankara, Turkey (Türkiye), 06018
- Sağlık Bilimleri Üniversitesi, Gülhane Fizyoterapi ve Rehabilitasyon Fakültesi
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Ankara, Turkey (Türkiye), 06560
- Gazi Üniversitesi Tıp Fakültesi Nöroloji Anabilim Dalı
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Having agreed to participate in the research after being given detailed information about the research.
- Having been diagnosed with Parkinson's disease by a specialist neurologist according to the UK Brain Bank criteria
- Being in stage 1-3 according to Hoehn & Yahr
- Being 40 years of age or older
Exclusion Criteria:
- Having a neurological condition other than Parkinson's disease
- Cognitive impairment
- Have undergone deep brain stimulation surgery
- Having a visual, auditory or perceptual problem
- Having any orthopedic, rheumatological or other disease that may affect walking and balance.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
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 |
|---|---|
|
Active Comparator: Contol Group
Single task training
|
Single task training with balance and walking exercises, twice a week for six weeks
|
|
Experimental: Variable priority dual task training group
Variable priority dual task training
|
Variable priority dual task training with balance and walking exercises performed simultaneously with cognitive tasks, twice a week for six weeks
|
|
Experimental: Fixed priority dual task training group
Fixed priority dual task training
|
Fixed priority dual task training with balance and walking exercises performed simultaneously with cognitive tasks, twice a week for six weeks
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Hoehn and Yahr Scale
Time Frame: Baseline, 6 weeks
|
A staging system that quickly provides information in determining the degree and symptom severity of the disease
|
Baseline, 6 weeks
|
|
Unified Parkinson's Disease Rating Scale
Time Frame: Baseline, 6 weeks
|
Evaluates cognitive skills, mood, activities of daily living, motor skills, motor fluctuations, dyskinesias, and autonomic dysfunction in four parts
|
Baseline, 6 weeks
|
|
Berg Balance Scale
Time Frame: Baseline, 6 weeks
|
It includes 14 functional activities to assess static and proactive balance.
The total score ranges from 0 to 56, with higher scores indicating better balance.
|
Baseline, 6 weeks
|
|
Functional Reach Test
Time Frame: Baseline, 6 weeks
|
The test is designed to assess dynamic balance by measuring the maximum distance that a person can reach forward beyond arm's length without taking a step.
|
Baseline, 6 weeks
|
|
Single Leg Stance Test
Time Frame: Baseline, 6 weeks
|
It is a test method used to evaluate static balance.
One foot is lifted without touching the supporting leg and the person is expected to maintain their balance for 30 seconds.
|
Baseline, 6 weeks
|
|
Four Square Step Test
Time Frame: Baseline, 6 weeks
|
It is a test method used to evaluate dynamic balance.
Two canes are placed on a flat surface to create 4 squares.
All squares are numbered.
The subject starts in one square and steps in one direction into each of the four squares and then reverses direction back to the start.
The time (in seconds) taken to complete the sequence is measured.
|
Baseline, 6 weeks
|
|
10 Meter Walk Test
Time Frame: Baseline, 6 weeks
|
Used to assess walking speed.
Participants are asked to walk a distance of 10 meters and the time taken is recorded.
|
Baseline, 6 weeks
|
|
Figure-of-Eight Walk Test
Time Frame: Baseline, 6 weeks
|
The participant stands still at the midpoint of two cones placed 1.52 m apart and begins walking around the cones in a figure eight at his/her usual pace.
The total time and number of steps taken to complete the test are recorded.
|
Baseline, 6 weeks
|
|
3-Meter Backward Walk Test
Time Frame: Baseline, 6 weeks
|
The 3-meter distance is measured and marked.
Participants are asked to walk backwards as quickly as possible with the "walk" command and to stop when they reach 3 meters.
The elapsed time is recorded in seconds.
|
Baseline, 6 weeks
|
|
Timed Up and Go Test
Time Frame: Baseline, 6 weeks
|
It is used to assess functional mobility level.
The participant is asked to stand up from the chair, walk 3 m, turn around, walk back to the chair and sit down.
The test starts with the "walk" command and the completion time is recorded in seconds.
|
Baseline, 6 weeks
|
|
Unified Parkinson's Disease Rating Scale, Part 2
Time Frame: Baseline, 6 weeks
|
UPDRS Part 2 generally is considered a psychometrically reliable tool for measuring activities of daily living outcomes in people with Parkinson's disease.
|
Baseline, 6 weeks
|
|
Dual Task Questionnaire
Time Frame: Baseline, 6 weeks
|
It is used to obtain information about the difficulties experienced in daily tasks related to dual task.
It consists of 10 questions, each question is scored between 0 and 4.
|
Baseline, 6 weeks
|
|
Trail Making Test
Time Frame: Baseline, 6 weeks
|
It is used to evaluate individuals' visual scanning speed, executive functions, visual-motor perception, motor function, planning, organization, abstract thinking and response limitation.
The test consists of 2 parts: A and B. In part A, the individual is asked to combine numbers from 1 to 25 and the completion time is recorded.
In part B, the individual completes the sequence by corresponding to a number and a letter, and the completion time is recorded.
|
Baseline, 6 weeks
|
|
Stroop Test
Time Frame: Baseline, 6 weeks
|
It is a test that evaluates executive functions and the suppression of inappropriate automatic responses and provides information about frontal functions.
|
Baseline, 6 weeks
|
|
Symbol Digit Modalities Test
Time Frame: Baseline, 6 weeks
|
It is a test that measures working memory and information processing speed.
In the upper right corner of the A4 paper used in the test, there is a grid of shapes, each representing a number.
In the other parts of the paper, there are randomly arranged shapes in blocks.
During the test, patients are asked to match these shapes with the numbers in the grid.
|
Baseline, 6 weeks
|
|
Word List Generation
Time Frame: Baseline, 6 weeks
|
It is a test used to evaluate complex attention functions and vocabulary.
It consists of animal and KAS sections.
First, the patient is asked to name every animal that comes to mind in one minute, as quickly as possible.
In the KAS section, the patient is asked to name every word that comes to mind, except for proper nouns and city names, with the letters K-A-S in order.
The time for each letter is again one minute.
|
Baseline, 6 weeks
|
|
Tampa Scale for Kinesiophobia
Time Frame: Baseline, 6 weeks
|
It is a 17-question scale developed to measure fear of movement/re-injury.
The scale includes parameters of injury/re-injury and fear-avoidance in work-related activities.
Each item is scored between 1-4.
|
Baseline, 6 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
February 1, 2024
Primary Completion (Actual)
September 30, 2025
Study Completion (Actual)
September 30, 2025
Study Registration Dates
First Submitted
January 21, 2025
First Submitted That Met QC Criteria
January 21, 2025
First Posted (Actual)
January 27, 2025
Study Record Updates
Last Update Posted (Estimated)
October 6, 2025
Last Update Submitted That Met QC Criteria
October 2, 2025
Last Verified
October 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 285 (National Heart, Lung, and Blood Institute)
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
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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