- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06636929
Effect of Problematic Smartphone Use
March 9, 2026 updated by: Ismail Okur, Kutahya Health Sciences University
Effect of Problematic Smartphone Use on Upper Extremity Functions and Cognitive Functions
There is no study that examines the effect of problematic use of smartphones, which has become a global problem today, on reaction time and cognitive functions together.
This study was planned to examine the effect of problematic smartphone use on upper extremity functions and cognitive functions.
Participants' problematic smartphone use will be evaluated with the Smartphone Addiction Scale Short Form.
Within the scope of upper extremity functions, Quick Disabilities of Arm, Shoulder & Hand Questionnaire, reaction time and grip strength will be evaluated.
Reaction time will be measured with BlazePod Trainer (Blazepod Trainer Device, Play Coyotta Ltd, Tel Aviv, Israel).
Jamar dynamometer (Performance Health, Warrenville, IL) will be used to evaluate grip strength.
Cognitive functions will be assessed using the Stroop Test ÇAPA Form, Trail Making Test and Cognitive Failures Questionnaire.
Study Overview
Status
Completed
Conditions
Study Type
Observational
Enrollment (Actual)
131
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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Center
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Kütahya, Center, Turkey (Türkiye), 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
- Adult
Accepts Healthy Volunteers
Yes
Sampling Method
Probability Sample
Study Population
Healthy adults aged 18-25 years
Description
Inclusion Criteria:
- To be between 18-25 years old
- Using a smartphone for at least 1 hour a day
- Volunteering to participate in the study
Exclusion Criteria:
- Having undergone a surgical operation involving the upper extremity within the last 6 months
- History of trauma to the shoulder, elbow, hand and wrist in the last 6 months
- Presence of a diagnosed neurological, rheumatic or psychiatric disease
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 |
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Study group
Participants with problematic smartphone use were identified with the Smartphone Addiction Scale Short Form.
Participants with a score above 31 for women and 33 for men were defined as individuals with problematic smartphone use.
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Control group
Participants with problematic smartphone use were identified with the Smartphone Addiction Scale Short Form.
Participants with a score below 31 for women and 33 for men were defined as the control group.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Smartphone Addiction Scale Short Form
Time Frame: Baseline
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It is a 10-item scale to assess problematic smartphone use.
Each item in the scale is scored between 1 (strongly disagree) and 6 (strongly agree).
The total score ranges from 10-60, with higher scores indicating an increased risk of smartphone addiction.
The cut-off score of the scale was reported as 33 for women and 31 for men.
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Baseline
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Upper Extremity Functions-Quick Disabilities of Arm, Shoulder & Hand (Quick DASH)
Time Frame: Baseline
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In the 11-question scale, difficulties encountered during activities of daily living (carrying shopping bags, opening jars, using a knife to cut food, etc.) due to problems in the shoulder, elbow and hand regions are scored from 1 (no difficulty) to 5 (no difficulty at all).
A higher total score indicates an increased level of functional limitation in the upper limb.
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Baseline
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Upper Extremity Functions-Reaction Time
Time Frame: Baseline
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The upper extremity reaction time will be assessed using the BlazePod Trainer (Blazepod Trainer Device, Play Coyotta Ltd, Tel Aviv, Israel).
Participants will be asked to hit 5 LEDs on a table as quickly as possible using only one hand while in a seated position.
The LEDs will be arranged in an arc on the table within the participant's reach without disturbing their seated posture.
The right and left hands will be evaluated separately.
The number of LEDs hit in 30 seconds, the unit hit time (ms), and the number of missed LEDs (those that automatically hit after a 5-second waiting period) will be recorded through the BlazePod app installed on the researchers' phones.
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Baseline
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Upper Extremity Functions-Grip Strength
Time Frame: Baseline
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A calibrated digital Jamar dynamometer (Performance Health, Warrenville, IL) will be used for grip strength.
Participants will be instructed to squeeze the dynamometer as hard as possible while sitting in an upright position as recommended by the American Society of Hand Therapists, with arms at their sides, elbows flexed 90° and forearms in a neutral position.
For hand grip strength, 3 measurements will be made with one minute intervals between each measurement and the average value will be recorded.
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Baseline
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Cognitive Functions-Stroop Test ÇAPA Form
Time Frame: Baseline
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It is used to assess executive functions such as attention, information processing speed and response inhibition.
The Stroop Test ÇAPA Form consists of a total of 60 items.
In the first part, there are small rectangles (0.5 x 1 cm) with colors such as yellow, blue and red.
In the second part, there are color names written in different colors.
The test is administered in 3 stages.
In the first part (Stroop A), the person is asked to name the colors in the boxes from left to right.
If a color blindness is detected, the test can be terminated.
In the second part (Stroop B), the person is asked to read quickly the color names written in different colors (yellow, red, green).
In the third part (Stroop C), participants are asked to say the colors of the words (blue, green, yellow) without reading the color names.
In all three parts, the time is timed and recorded with a stopwatch.
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Baseline
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Cognitive Functions-Trail Making Test
Time Frame: Baseline
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It is used to assess cognitive functions such as working memory, complex attention and cognitive flexibility.
It requires visual scanning and hand-eye coordination.
The Trail Making Test consists of 25 circles with numbers distributed on paper and has 2 sections (IST A-B).
Section A contains numbers numbered between 1 and 25, and during the test, individuals are asked to connect the circles by drawing lines consecutively and in the correct order.
In part B, the circles contain both numbers and letters.
Participants are asked to quickly connect the circles in consecutive order in accordance with the order of numbers and letters (1-A, 2-B, 3-C, etc.) by drawing a line without lifting the pencil from the paper.
The time to complete each trace is recorded in seconds (s), A and B.
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Baseline
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Cognitive Functions-Cognitive Failures Questionnaire
Time Frame: Baseline
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Errors in perception, memory and motor functions in daily life are assessed with 25 questions.
Each question is scored from 0 (never) to 4 (very often).
The total score ranges from 0-100, with a higher score indicating an increased level of cognitive error.
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Baseline
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Ismail Okur, PT, 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)
October 20, 2024
Primary Completion (Actual)
June 30, 2025
Study Completion (Actual)
December 31, 2025
Study Registration Dates
First Submitted
October 8, 2024
First Submitted That Met QC Criteria
October 10, 2024
First Posted (Actual)
October 15, 2024
Study Record Updates
Last Update Posted (Actual)
March 10, 2026
Last Update Submitted That Met QC Criteria
March 9, 2026
Last Verified
March 1, 2026
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- KSBU 2024/04-27
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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