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Smartphone AddictionNCT06636929

Effect of Problematic Smartphone Use

An observational study of Smartphone Addiction, run by Kutahya Health Sciences University at 1 site in Turkey (Türkiye).

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

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. Read more about this study

Who is it for?
Ages 18 to 25 yearsHealthy volunteers can take part
Conditions the study is for
Smartphone Addiction
How many people
131 participants
Where
1 siteTurkey (Türkiye)
Study dates
20 Oct 2024to 31 Dec 2025
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 25 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Study population: Healthy adults aged 18-25 years

Who may be able to join

  • To be between 18-25 years old
  • Using a smartphone for at least 1 hour a day
  • Volunteering to participate in the study

Who cannot join

  • 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

Trial locations and contacts

1 site in 1 country.

Turkey (Türkiye)1 site
  • Kutahya Health Sciences University

    Kütahya, Center, 43100

Other trials in Turkey (Türkiye)

About this study

Official title: 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.

Keywords
problematic smartphone use, smartphone addiction, cognitive function, reaction time, upper extremity problem
Medical subject headings
Internet Addiction Disorder

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT06636929
Study groupRoleWhat they receive
Study groupParticipants 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.
Control groupParticipants 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.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Smartphone Addiction Scale Short Form

    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.

    Measured: Baseline

  2. Upper Extremity Functions-Quick Disabilities of Arm, Shoulder & Hand (Quick DASH)

    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.

    Measured: Baseline

  3. Upper Extremity Functions-Reaction Time

    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.

    Measured: Baseline

  4. Upper Extremity Functions-Grip Strength

    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.

    Measured: Baseline

  5. Cognitive Functions-Stroop Test ÇAPA Form

    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.

    Measured: Baseline

  6. Cognitive Functions-Trail Making Test

    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.

    Measured: Baseline

  7. Cognitive Functions-Cognitive Failures Questionnaire

    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.

    Measured: Baseline

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted15 Oct 2024
  2. Study start20 Oct 2024
  3. Primary completion30 Jun 2025
  4. Study completion31 Dec 2025

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Case-control
Time perspective
Cross-sectional
Enrolment
131 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06636929
Sponsor's protocol ID
KSBU 2024/04-27
Status last verified
Mar 2026
First submitted
8 Oct 2024
Last updated
10 Mar 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

An observational study of Smartphone Addiction, run by Kutahya Health Sciences University at 1 site in Turkey (Türkiye).

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 10 Mar 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Smartphone Addiction Scale Short Form (time frame: Baseline). The study lists 7 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 10 Mar 2026.

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