- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07107620
- Original Trial
Dual Task Performance and Type II Diabetes Mellitus
August 4, 2025 updated by: Abdulkadir Ertürk, Kahramanmaras Sutcu Imam University
Investigation of Dual Task Performance of Individuals With Type 2 Diabetes Mellitus
The aim of this study is to compare the dual task performances of individuals with and without type 2 diabetes.
Thus, it will be concluded whether having type 2 diabetes affects dual task performance.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
In our daily lives, we often have to juggle many tasks simultaneously.
Performing two tasks simultaneously is called dual-tasking.
The ability to perform two tasks simultaneously is called dual-tasking performance.
Dual-tasking performance can decrease in individuals with diabetes due to complications of diabetes.
This study compared the dual-tasking performance of individuals with type 2 diabetes and healthy individuals using dual-tasking tests categorized as easy, medium, and difficult.
Study Type
Observational
Enrollment (Actual)
141
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
-
-
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Denizli, Turkey
- Pamukkale University Hospital
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-
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
Yes
Sampling Method
Probability Sample
Study Population
Individuals who have had diabetes for at least 1 year and are over 50 years of age and their matched healthy controls constitute the study sample.
Description
Inclusion Criteria:
- Having been diagnosed with Type II DM (for the Type II diabetes group)
- Being 50 years old or older
- Being a native Turkish speaker
Exclusion Criteria:
Not being able to read and write,
- Having communication problems,
- Having a score below 24 points on the Standardized Mini-Mental Test,
- Having one of the neurological diseases that will affect the study such as Parkinson's, stroke, etc.,
- Having upper and/or lower extremity surgery in the last year or having a surgical history that will affect walking,
- Having retinopathy, foot ulcers, and severe sensory impairment
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
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
type II diabetes mellitus group
Dual task tests were applied to the group with type 2 diabetes mellitus
|
Single task tests consist of measuring walking times with normal walking (easy), walking with a 50% reduction in the base of support measured between the medial malleoli (medium difficulty) and tandem walking (difficult) tasks while applying the 10 meter walk test and time up go tests.
Dual task consists of single task plus tests of carrying glasses of water or counting backwards from a given number.
|
|
Healthy group
Dual task tests were administered to the healthy group
|
Single task tests consist of measuring walking times with normal walking (easy), walking with a 50% reduction in the base of support measured between the medial malleoli (medium difficulty) and tandem walking (difficult) tasks while applying the 10 meter walk test and time up go tests.
Dual task consists of single task plus tests of carrying glasses of water or counting backwards from a given number.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
10 meter walk test
Time Frame: one day
|
The dual task cost was calculated to measure dual task performance by applying the 10-meter walking test as single and dual tasks. This cost will be calculated as follows: (Dual task performance-single task performance)/ single task performance x100 |
one day
|
|
time up go test
Time Frame: one day
|
The dual task cost was calculated to measure dual task performance by applying the time up go test as single and dual tasks.
This cost will be calculated as follows: (Dual task performance-single task performance)/ single task performance x100
|
one day
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Stroop test
Time Frame: one day
|
There are 5 sections in this test.
Section 1 includes reading black text, section 2 includes reading colored words related to color names, section 3 includes saying the color of shapes, section 4 includes saying the color of words that are not color names, and section 5 includes saying the color of colored words that are color names.
Individuals are asked to read from left to right as fast as possible.
The time taken is recorded in seconds.
|
one day
|
|
Dual task survey
Time Frame: one day
|
It is a test that questions the difficulties experienced by individuals during dual-task activities in daily life activities.
The survey consists of 10 questions.
The short duration of the survey is an advantage.
The survey, which consists of 5 answers, is scored between 0 and 4. A score of ''4'' indicates that difficulties are experienced very often, ''0'' indicates that there is no difficulty.
|
one day
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Study Director: Suat EREL, professor, Pamukkale University Faculty of Health Sciences
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)
September 1, 2022
Primary Completion (Actual)
March 1, 2023
Study Completion (Actual)
June 1, 2023
Study Registration Dates
First Submitted
June 28, 2025
First Submitted That Met QC Criteria
August 4, 2025
First Posted (Actual)
August 6, 2025
Study Record Updates
Last Update Posted (Actual)
August 6, 2025
Last Update Submitted That Met QC Criteria
August 4, 2025
Last Verified
July 1, 2025
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- KSÜKADİRERTÜRK1
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
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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