- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07540546
Smartphone Use and Hand Function in Young Adults
April 18, 2026 updated by: ESRA PEHLIVAN, Saglik Bilimleri Universitesi
The Relationship Between Daily Smartphone Use Duration and Dominant Hand Grip Strength, Thumb Strength, Wrist and Thumb Proprioception in Young Adults
This observational cross-sectional study aims to investigate the relationship between daily smartphone usage duration and hand function parameters in young adults.
Specifically, the study will examine the association between smartphone screen time and dominant hand grip strength, thumb strength, and wrist and thumb proprioception.
Healthy individuals aged 18-35 years will be included.
All participants will undergo a single-session assessment including measurement of smartphone usage duration, hand grip strength, pinch strength, and joint position sense of the wrist and thumb.
The findings are expected to provide insight into the potential effects of prolonged smartphone use on hand function and proprioceptive performance in young adults.
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Detailed Description
The widespread use of smartphones in daily life has increased significantly, particularly among young adults.
While these devices provide convenience and accessibility, excessive smartphone use has been associated with various musculoskeletal and functional impairments, particularly in the upper extremity.
Repetitive thumb movements, sustained grip positions, and prolonged device use may negatively affect muscle strength, joint proprioception, and overall hand function.
Previous studies have reported that excessive smartphone use may lead to decreased grip strength, altered thumb mechanics, and impaired proprioception.
However, there is limited research directly examining the relationship between objectively measured smartphone usage duration and detailed hand function parameters.
This study is designed as a cross-sectional, observational, and analytical investigation.
Healthy individuals aged 18-35 years will be recruited.
Participants with a history of upper extremity injury, neurological disease, or musculoskeletal disorders affecting the hand and wrist will be excluded.
All participants will be evaluated in a single session.
Demographic data and clinical history will be recorded.
Smartphone usage duration will be obtained from built-in device tracking systems (Screen Time for iOS and Digital Wellbeing for Android) based on the last 7 days of use.
Study Type
Observational
Enrollment (Estimated)
84
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: Esra Pehlivan
- Phone Number: +90 0216 777 8 777
- Email: esra.pehlivan@sbu.edu.tr
Study Contact Backup
- Name: Sümeyra Köseoğlu
- Phone Number: +90 0216 777 8 777
- Email: sumeyrakoseoglu655@gmail.com
Study Locations
-
-
Uskudar
-
Istanbul, Uskudar, Turkey (Türkiye), 34668
- Saglik Bilimleri Universitesi
-
Contact:
- Esra Pehlivan
- Email: fztesrakambur@yahoo.com
-
-
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
Non-Probability Sample
Study Population
Healthy Universitty Student
Description
Inclusion Criteria:
- Healthy adults
- Aged between 18 and 35 years
- Voluntary participation in the study
Exclusion Criteria:
- History of hand or wrist surgery
- Fracture or serious injury in the hand/thumb within the last 6 months
- Neurological disorders
- Rheumatologic diseases
- Cognitive impairment preventing understanding of instructions
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 |
Intervention / Treatment |
|---|---|
|
Observational Group: Smartphone-Addicted Participants
Participants classified as having smartphone addiction according to the Smartphone Addiction Scale-Short Form will undergo a single-session assessment including daily smartphone screen time, dominant hand grip strength, thumb pinch strength, wrist joint position sense, and thumb joint position sense.
|
All participants will undergo a standardized assessment protocol including measurement of smartphone addiction level, daily smartphone screen time from the past 7 days, dominant hand grip strength, thumb pinch strength, wrist proprioception, and thumb proprioception in a single session
|
|
Observational Group: Non-Addicted Participants
Participants classified as not having smartphone addiction according to the Smartphone Addiction Scale-Short Form will undergo the same single-session assessment including daily smartphone screen time, dominant hand grip strength, thumb pinch strength, wrist joint position sense, and thumb joint position sense.
|
All participants will undergo a standardized assessment protocol including measurement of smartphone addiction level, daily smartphone screen time from the past 7 days, dominant hand grip strength, thumb pinch strength, wrist proprioception, and thumb proprioception in a single session
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Hand Grip Strength
Time Frame: Single assessment at baseline
|
Hand grip strength will be measured using a hydraulic hand dynamometer.
The participant will be in a seated position with the elbow flexed at 90 degrees.
Three measurements will be taken with a 10-second rest between each, and the average value will be recorded in kilograms (kg).
|
Single assessment at baseline
|
|
Thumb Pinch Strength
Time Frame: Single assessment at baseline
|
Thumb muscle strength will be measured using a pinchmeter.
The participant will be seated with the elbow flexed at 90 degrees and the wrist in a neutral position.
The average of three trials will be recorded in kilograms (kg).
|
Single assessment at baseline
|
|
Thumb Active Joint Position Sense (JPS)
Time Frame: Single assessment at baseline
|
Measured using a standard transparent plastic goniometer.
The researcher will passively move the thumb to a 30-degree abduction target position.
The participant will be asked to actively reproduce this angle.
The absolute error between the target angle and the reproduced angle will be recorded in degrees.
|
Single assessment at baseline
|
|
Wrist Joint Position Sense (JPS)
Time Frame: Single assessment at baseline
|
Measured using a goniometer with the participant's eyes closed.
The wrist will be passively moved to predetermined positions (30 degrees flexion, 30 degrees extension, 10 degrees radial deviation, and 15 degrees ulnar deviation).
The participant will then actively reposition the wrist, and the absolute error will be calculated in degrees.
|
Single assessment at baseline
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Smartphone Screen Time
Time Frame: Single assessment at baseline
|
Objective measurements of the participants' smartphone use over the last 7 days will be obtained.
Data will be collected using built-in features such as "Screen Time" for iOS devices or "Digital Wellbeing" for Android devices.
|
Single assessment at baseline
|
|
Smartphone Addiction Scale-Short Form
Time Frame: Single assessment at baseline
|
The Smartphone Addiction Scale-Short Form (SAS-SF) was used to assess smartphone addiction.
The scale comprises 10 items rated on a 6-point Likert scale (1 = strongly disagree to 6 = strongly agree), yielding a total score between 10 and 60.
Higher scores reflect a higher risk or severity of smartphone addiction.
|
Single assessment at baseline
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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 (Estimated)
May 1, 2026
Primary Completion (Estimated)
May 1, 2027
Study Completion (Estimated)
May 1, 2027
Study Registration Dates
First Submitted
April 13, 2026
First Submitted That Met QC Criteria
April 13, 2026
First Posted (Actual)
April 20, 2026
Study Record Updates
Last Update Posted (Actual)
April 22, 2026
Last Update Submitted That Met QC Criteria
April 18, 2026
Last Verified
April 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Smartphone&Proprioception1
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
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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