- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04783740
Validity and Reliability of Turkish Version of The Working Memory Questionnaire
March 28, 2022 updated by: Lütfiye AKKURT, MSc, Kutahya Health Sciences University
The aim of this study was to determine the Turkish validity and reliability of ''The Working Memory Questionnaire'' developed by Dr. Vallat-Azouvi.
Study Overview
Status
Completed
Conditions
Detailed Description
Working Memory refers to the temporary storage and exchange of information required for complex tasks such as language, understanding, learning, and reasoning.
Working memory deficits are worse in people with advanced age and low education.
In addition, working memory is impaired in children with traumatic brain injury, stroke, Alzheimer's disease, and attention deficit hyperactivity disorder.
The aim of this study is to determine the Turkish version, validity, and reliability of ''The Working Memory Questionnaire''.
300 health people will include in the study.
In order to determine the reliability of the scale, the intraclass correlation coefficient (ICC) will be used to determine the level of the relationship between the results of the first and second measurements.
Cronbach's alpha coefficient will be used for the homogeneity of the questions in the scale.
For construct validity, the correlation coefficient will be used to determine the agreement between the Turkish Version of Cognitive Failures Questionnaire and The Working Memory Questionnaire.
Study Type
Observational
Enrollment (Actual)
303
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
-
-
Merkez
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Kütahya, Merkez, Turkey, 43100
- Kutahya Health Sciences University
-
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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 50 years (ADULT)
Accepts Healthy Volunteers
N/A
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Individuals living in Turkey
Description
Inclusion Criteria:
- Being an individual between the ages of 18-50
Exclusion Criteria:
- Having a neurological and mental illness
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The Working Memory Questionnaire
Time Frame: 15 minute
|
The Working Memory Questionnaire has been designed by Dr. Vallat-Azouvi at el. specifically to assess everyday life difficulties related to working memory failures.
It consists of 30 statements rated on a 5-point Likert-type scale ranging from "not at all" to "extremely".
WMQ is consists of 3 subscales, there are storage, attention, and executive domains.The total score ranges from 0-120 points.
Higher scores correspond to more self-identified difficulties
|
15 minute
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Turkish Version Cognitive Failures Questionnaire
Time Frame: 12 minute
|
The Cognitive Failures Questionnaire (CFQ) is a self-report questionnaire to assess failures of perception, motor function, and memory.
CFQ is consists of 25 items and 5 points Likert-type scale.
The total score is ranges from 0-100 points.
|
12 minute
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: İsmail SARAÇOĞLU, PhD, Kutahya Health Sciences University
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)
March 3, 2021
Primary Completion (ACTUAL)
September 3, 2021
Study Completion (ACTUAL)
December 30, 2021
Study Registration Dates
First Submitted
March 3, 2021
First Submitted That Met QC Criteria
March 3, 2021
First Posted (ACTUAL)
March 5, 2021
Study Record Updates
Last Update Posted (ACTUAL)
March 29, 2022
Last Update Submitted That Met QC Criteria
March 28, 2022
Last Verified
March 1, 2021
More Information
Terms related to this study
Other Study ID Numbers
- KutahyaHSU
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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