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

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
      • 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.

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

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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