- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05952362
The Effect of Smartphone Addiction and Mental Fatigue on Working Memory in University Students
November 8, 2023 updated by: Kutahya Health Sciences University
The aim of this study is to investigate the effects of smartphone addiction and mental fatigue on working memory in university students.
Study Overview
Status
Completed
Conditions
Detailed Description
University students who meet the inclusion and exclusion criteria will be informed about the study and the participants who agree to participate in the study will be given the Turkish version of "Smartphone Addiction Scale", ''Mental Fatigue Scale'' and "Working Memory Questionnaire" tests, respectively.
120 university students will included in the study.
To evaluate between correlation of tests will used to correlation analysis tests.
In addition, it will be investigated whether there is a difference between 1.2.3 and 4th grades in terms of Smartphone Addiction, Mental Fatigue Scale and Working Memory Questionnaire
Study Type
Observational
Enrollment (Actual)
120
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Lütfiye AKKURT, PhD
- Phone Number: 0902742600043
- Email: lutfiye.akkurt@ksbu.edu.tr
Study Contact Backup
- Name: Cihan Caner AKSOY, PhD
- Phone Number: 0902742600043
- Email: cihancaner.aksoy@ksbu.edu.tr
Study Locations
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Kutahya, Turkey
- Kütahya 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
- Adult
Accepts Healthy Volunteers
Yes
Sampling Method
Probability Sample
Study Population
120 university students
Description
Inclusion Criteria:
- Being a university student
- Be between the ages of 18-25
- Using a smartphone for at least one hour a day
Exclusion Criteria:
- Having musculoskeletal pain
- Having had surgery in the last 6 months
- Decline to participate in the study
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 |
---|---|---|
Working Memory Questionnaire
Time Frame: Baseline (First assessment)
|
The Working Memory Questionnaire (WMQ) is a self-administered scale proposed by Vallat-Azouvi.
It assesses the three different working memory domains (memory storage, attention, and executive functions).
It consists of 30 questions, each scored on a five-point Likert-type scale ranging from 0 (not at all) to 4 (extremely).
The total score varies between 0 and 120.
Higher scores represent more memory difficulties/complaints.
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Baseline (First assessment)
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Smartphone Addicition Scale-Short Version
Time Frame: Baseline (First assessment)
|
This instrument to examine smartphone addiction was developed by Kwon et al.
This scale consisted of six factors with ten items each, rated using the six-point Likert scale (1: strongly disagree, 2: disagree, 3: weakly disagree, 4: weakly agree, 5: agree, and 6: strongly agree).
|
Baseline (First assessment)
|
Mental Fatigue Scale
Time Frame: Baseline (First assessment)
|
The Mental Fatigue Scale (MFS) is a 15-item questionnaire that specifically evaluates mental fatigue.
It includes affective, cognitive and sensory symptoms, duration of sleep and daytime variation in symptom severity.
It has a 7-point Likert-type scale and is scored between 0 and 3. A rating of 0 indicates normal function, 1 slight problem, 2 significant problems and 3 maximum problems.
There are also items such as 0.5, 1.5, 2.5 for marking when individuals fall between 2 items (0.5, 1.5, 2.5).
The total score of the scale is obtained by summing the scores of the first 14 questions.
The last question is evaluated as yes or no.
The scores range from 0 to 42 and 0-10 indicates no mental fatigue problem, 10.5-14.5 indicates slight mental fatigue, 15-20 indicates fairly serious mental fatigue, and ≥ 20.5 indicates serious mental fatigue
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Baseline (First assessment)
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Cihan Caner AKSOY, PhD, Kütahya Health Sciences University
- Study Director: Lütfiye AKKURT, PhD, Kütahya 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)
June 15, 2023
Primary Completion (Actual)
November 7, 2023
Study Completion (Actual)
November 7, 2023
Study Registration Dates
First Submitted
July 11, 2023
First Submitted That Met QC Criteria
July 11, 2023
First Posted (Actual)
July 19, 2023
Study Record Updates
Last Update Posted (Estimated)
November 9, 2023
Last Update Submitted That Met QC Criteria
November 8, 2023
Last Verified
July 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2023/07-08
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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