The Effect of Smartphone and Hand Anthropometry on Pain and Upper Extremity Functions

June 23, 2025 updated by: Feyza Altindal Karabulut, Nigde Omer Halisdemir University
Mobile phones have different uses in different disciplines, and this encourages long-term use. For optimum comfort use, it is important to ensure users' awareness when purchasing mobile phones that match their hand sizes. The number of studies in the literature on this subject is limited. In this context, the aim of our study is to investigate the relationship between smartphone and hand anthropometry measurements and upper extremity pain and functions.

Study Overview

Status

Completed

Detailed Description

Phone design features cause different problems on body mechanics and musculoskeletal system. With the use of smartphones, people tend to maintain incorrect postures for long periods of time, which increases tension in the body. This situation causes complaints such as cervical disc herniation, tingling complaints in different body parts, overuse injuries, Upper Crosses syndrome, and carpal tunnel syndrome. On the other hand, the use of smartphones is increasing among students for reasons such as providing students with freedom of time and space, increasing the speed of teaching and learning, supporting one-on-one learning, and increasing the number of ideas produced by encouraging a group discussion environment.

Mobile phones have different uses in different disciplines, and this encourages long-term use. Although many musculoskeletal system structures can be affected by incorrect postures due to the long-term use of smart mobile phones, it is thought that the upper extremity is most affected. Therefore, the aim of our study is to investigate the relationship between smartphone dimensions and hand anthropometric measurements and upper extremity pain and functions in order to raise awareness when purchasing mobile phones that match users' hand sizes for optimum comfort and use.

Study Type

Observational

Enrollment (Actual)

435

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

    • Nigde
      • Niğde, Nigde, Turkey, 51700
        • Nigde Omer Halisdemir University, Bor Faculty of Health Sciences

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

  • Child
  • Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

Volunteer participants include students and staff studying in different departments at the university.

Description

Inclusion Criteria:

  • Sending at least 5 e-mails or text messages a day from your mobile phone,
  • Using a smartphone for more than 1 hour a day to play games or browse the internet

Exclusion Criteria:

  • Having an existing injury in the hand or upper extremity (suffered 6 months ago)
  • Having been diagnosed with a degenerative, inflammatory, musculoskeletal, neuromuscular, or congenital disorder of the hand or upper extremity.

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
Sample of Study
Volunteer participants who constitute the study sample include students and staff studying in different departments at the university. Inclusion criteria; It includes using a smartphone for more than 1 hour a day to send at least 5 emails or text messages a day, play games or browse the internet. Exclusion criteria; It includes students who have an existing injury to the hand or upper extremity (6 months ago) and who have been diagnosed with degenerative, inflammatory, musculoskeletal, neuromuscular and congenital disorders of the hand or upper extremity that affect their use in daily life.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Hand anthropometric measurements: Hand length
Time Frame: 2 month
It is the longitudinal distance in centimeters from the midpoint of the distance from the most distal styloid process of the radius to the most distal styloid process of the ulna to the tip of the 3rd finger. Measurements will be made with the participants sitting on a chair, with their hands held on a horizontal platform. While the fingers are kept as close to each other as possible in all measurements, participants will be asked to open their hands as much as they can only in the maximum hand spread measurement.
2 month
Hand anthropometric measurements: Palm length
Time Frame: 2 month
It is the longitudinal distance in centimeters between the midpoint of the wrist crease and the highest point of the 3rd Metacarpal head. Measurements will be made with the participants sitting on a chair, with their hands held on a horizontal platform. While the fingers are kept as close to each other as possible in all measurements, participants will be asked to open their hands as much as they can only in the maximum hand spread measurement.
2 month
Hand anthropometric measurements: Width of the hand (Metacarpal)
Time Frame: 2 month
It is the longitudinal distance in centimeters between the base of the 2nd Metacarpal bone and the base of the 5th Metacarpal bone. Measurements will be made with the participants sitting on a chair, with their hands held on a horizontal platform. While the fingers are kept as close to each other as possible in all measurements, participants will be asked to open their hands as much as they can only in the maximum hand spread measurement.
2 month
Hand anthropometric measurements: Maximum hand spread measurement
Time Frame: 2 month
It is the longest distance in centimeters from the thumb to the tip of the 5th finger when your hand is open. Measurements will be made with the participants sitting on a chair, with their hands held on a horizontal platform. While the fingers are kept as close to each other as possible in all measurements, participants will be asked to open their hands as much as they can only in the maximum hand spread measurement.
2 month
Gross grip strength measurement
Time Frame: 2 month
Grip strength will be measured in Newton using a Hydraulic Hand Dynamometer. Standard grip strength testing position recommended by the American Society of Hand Therapists (ASHT); Participants will sit upright on the back of a chair without armrests with their feet flat on the floor, shoulder in adduction and neutral rotation, elbow in 90 degree flexion, forearm in neutral, wrist in slight extension and (0-150) degree ulnar deviation. It will be measured 3 times, and a 1-minute rest break will be given between each trial. The average of 3 attempts will be calculated for each hand.
2 month
Pinch grip strength
Time Frame: 2 month
Measurement of pinch grip strength in Newton will be performed with a digital pinchmeter. Pinch grip strength test position recommended by the American Society of Hand Therapists (ASHT); Participants will sit upright on the back of a chair without armrests with their feet flat on the floor, shoulder adduction and neutral rotation, elbow 90 degree flexion, forearm neutral, wrist slightly extended and (0-150) degree ulnar deviation. It will be measured 3 times, and a 1-minute rest break will be given between each trial. The average of 3 attempts will be calculated for each hand.
2 month
Measurement of phone dimensions
Time Frame: 2 month
The size of the touch screen will be measured in inches diagonally from one corner of the screen to the opposite corner (6). iPhone 5 models from Apple and 6 models from Samsung Galaxy, Realme, Xiaomi Redmi, Oppo, Huawei, Infinix, Reeder and other touch screen phones will be used. Screen dimensions will be measured using a standard ruler 30 cm diagonally across the screen (3). According to screen size, mobile phones will be grouped into small, medium and large phone sizes as shown in Table 2.
2 month
Upper extremity functional status assessment
Time Frame: 2 month
Quick-DASH is an evaluation questionnaire that measures activity and participation limitations in all upper extremity disorders. In the survey, patients' difficulties during daily living activities are questioned with 11 questions. Each answer is scored on a Likert scale from 1 to 5, from best to worst. There are also optionally completed Business Model (DASH-W) sections consisting of 4 questions and Sports and Musicians Model (DASH-SM) sections consisting of 4 questions. The validity and reliability of this questionnaire in Turkish was determined by Düger et al. made by. The total score for the first section consisting of 30 questions varies between 0 and 100. The total score for the second part ranges from 0 to 100. For the third part, which evaluates high performance sports, the total score varies between 0 and 100. An increase in the score in the survey indicates a decrease in functionality.
2 month

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Pain assessment
Time Frame: 2 month
Visual Analog Scale (VAS) Standard 10 centimeters VAS (0 = "no pain", 10 = "unbearable pain") was used to determine the pain levels of the volunteers participating in the study.
2 month
Smartphone addiction
Time Frame: 2 month
In our study, the Smartphone Addiction Scale Short Form, whose Turkish adaptation is valid and reliable, will be used to measure the smartphone addiction of the participants. The total number of items of this single-factor scale is 10. The scale is evaluated with a six-point Likert-type scale, and each item is scored from one (strongly disagree) to six (strongly agree). The lowest score that can be obtained from this scale is 10 and the highest score is 60. The cut-off value for the scale was found to be 31 points for men and 33 points for women. High scores from the scale indicate an increased risk of smartphone addiction.
2 month

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Altindal Karabulut, Asst. Prof., Nigde Omer Halisdemir University
  • Study Chair: Nihal BUKER, Prof., Pamukkale University

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

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)

May 13, 2024

Primary Completion (Actual)

September 30, 2024

Study Completion (Actual)

September 30, 2024

Study Registration Dates

First Submitted

April 2, 2024

First Submitted That Met QC Criteria

April 17, 2024

First Posted (Actual)

April 18, 2024

Study Record Updates

Last Update Posted (Actual)

June 26, 2025

Last Update Submitted That Met QC Criteria

June 23, 2025

Last Verified

June 1, 2025

More Information

Terms related to this study

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

product manufactured in and exported from the U.S.

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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