- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05188937
Validity and Reliability of the Dual-task Questionnaire
May 25, 2022 updated by: Sefa Eldemir, Gazi University
Validity and Reliability of the Dual-task Questionnaire in Multiple Sclerosis Patients
It is important to increase the independence of Multiple Sclerosis (MS) patients in activities of daily living.
Almost all activities of daily living require managing many activities at the same time.
For example, walking or standing while talking on the phone.
There is a need for easily applicable, reliable and valid scales to evaluate dual-task performance in MS patients.
Therefore, the aim of this study is to establish the Turkish cultural adaptation, validity and reliability of the Dual-Task Questionnaire scale in MS patients.
This study included a total of 50 patients with MS [age (18-65) years].
Dual-task Questionnaire (DTQ), Timed Up and Go test (TUG) with dual-task and Nine Hole Peg test (9-HPT) with dual-task were applied to the patients.
The second evaluation (retest) was carried out by the same physiotherapist one week following the first evaluation (test) in order to measure test-retest reliability.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
This study included patients with MS between 0-5,5 score according to the Extended Disability Status Scale (EDSS).
DTQ was used to assess the frequency of difficulties associated with daily tasks involving the dual-task.
Additionally TUG with dual-task and 9-HPT with dual-task were applied to the patients.
An experienced physiotherapist applied all these tests.
In order to measure test-retest reliability, a retest was carried out by the same physiotherapist one week following the first evaluation.
The construct validity of DTQ was tested by Pearson's correlation coefficient.
Study Type
Interventional
Enrollment (Actual)
50
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
-
-
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Ankara, Turkey
- Gazi University, Faculty of Health Sciences, Department of Physiotherapy and Rehabilitation
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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
18 years to 65 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Clinical diagnosis of Multiple Sclerosis
- Must be able to ambulatory status (Expanded Disability Status Scale score ≤ 6 )
- No relapse in the last 3 mounts
Exclusion Criteria:
- Orthopedic problems
- Visual, perception, and hearing problems
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: Prevention
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: validity and reliability of Dual-task Questionnaire
This study was conducted as "test-retest" design and the psychometric properties of Dual-task Questionnaire were examined in patients with MS.
|
Validity and reliability assessment of the Dual-task Questionnaire
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Validity and reliability of Dual-Task Questionnaire in patients with MS
Time Frame: one week
|
Validity and reliability
|
one week
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the 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, 2021
Primary Completion (Actual)
October 1, 2021
Study Completion (Actual)
May 5, 2022
Study Registration Dates
First Submitted
December 27, 2021
First Submitted That Met QC Criteria
December 27, 2021
First Posted (Actual)
January 12, 2022
Study Record Updates
Last Update Posted (Actual)
May 27, 2022
Last Update Submitted That Met QC Criteria
May 25, 2022
Last Verified
May 1, 2022
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 1- MS-DTQ-VALİDİTY
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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