Tonus, Stiffness and Elasticity of Hand and Wrist Muscles in Smartphone Addiction

February 12, 2025 updated by: Hazel Çelik Güzel, Bandırma Onyedi Eylül University

Investigation of Tonus, Stiffness and Elasticity of Hand and Wrist Muscles in Intensive Smartphone Use

The aim of this study was to investigate the tonus, stiffness and elasticity of the hand and wrist muscles in intensive smartphone use.

Study Overview

Detailed Description

Consent was obtained from the students with the 'Informed Voluntary Consent Form' and the sociodemographic data of the students were recorded on the previously prepared Descriptive Data Form. The students were asked to fill out the Smartphone Addiction Scale-Short Form. Before starting the clinical evaluation, anamnesis was taken from the students and their general health status, phone usage time (minutes) and exclusion criteria were questioned. Myotone evaluations of the tenar region, flexor carpi radialis, flexor carpi ulnaris, extensor digitorum, extensor carpi radialis and extensor carpi ulnaris muscles were performed. Then, the standard grip strength of the dominant and non-dominant side hand was evaluated with Saehan hand dynamometer and the lateral grip strength of the thumb was evaluated with Saehan pinchmeter.

Study Type

Observational

Enrollment (Actual)

56

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

      • Balikesir, Turkey, 10200
        • Bandırma Onyedi Eylül University

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

University students

Description

Inclusion Criteria:

  • To study at Bandirma Onyedi Eylül University
  • Students between the ages of 18-30 years, whose voluntary consent was obtained and who use smartphones

Exclusion Criteria:

  • Individuals with musculoskeletal system problems such as fractures of the hand, fingers and upper extremities, rheumatoid disease with evidence of systemic, specific pathological conditions
  • Individuals who have undergone any surgical operation related to hand, finger and upper extremity problems
  • Individuals who have received hand, finger and upper extremity related physiotherapy and rehabilitation services in less than 6 months
  • Individuals with diagnosed psychiatric illness.

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
Smartphone Addiction Scale-Short Form
Time Frame: May 1, 2024- January 1, 2025
Smartphone Addiction Scale-Short Form: In our study, the Smartphone Addiction Scale-Short Form will be filled out in order to evaluate the intensity of smartphone use of students, and the daily duration of smartphone use will be recorded. The scale is a 6-point Likert-type scale consisting of 10 items used to measure the risk of smartphone addiction. Scores obtained from the scale vary between 10-60 and an increase in the score indicates an increased risk for smartphone addiction. The cut-off score of the scale was determined as 31 for men and 33 for women. In the Turkish validity and reliability study, Cronbach's alpha coefficient was found to be 0.86.
May 1, 2024- January 1, 2025
Hand grip strength assessment
Time Frame: May 1, 2024- January 1, 2025
Hand grip strength was measured with 'Saehan Hydraulic Hand Dynamometer'. Participants were informed about the correct holding position and use of the instrument. In the measured arm, the position of 90̊ flexion from the elbow joint and completely adjacent to the body was used. The participant's hand was placed in the second grip position of the dynamometer and asked to make the strongest grip he/she could make, right and left measurements were taken.
May 1, 2024- January 1, 2025
Finger lateral grip strength assessment
Time Frame: May 1, 2024- January 1, 2025
Finger lateral grip strength was measured with 'Saehan Hydraulic pinch gauge'. Participants were informed about the correct holding position and use of the instrument. While the participant was sitting on a chair with arms supported, the shoulder was adjacent to the trunk and neutral, the elbow joint was in 90 ̊ flexion, the forearm was neutral, the wrist was in 0-30 ̊ extension and 0-15 ̊ ulnar deviation. Right and left finger lateral grip measurements were taken.
May 1, 2024- January 1, 2025
Myoton assessment
Time Frame: May 1, 2024- January 1, 2025
Myoton PRO device was used to objectively evaluate the biomechanical properties of the hand and wrist muscles such as tone, stiffness and elasticity. Tenar region, flexor carpi radialis, flexor carpi ulnaris, extensor digitorum, extensor carpi radialis and extensor carpi ulnaris muscles were evaluated bilaterally. Three measurements were recorded at one second intervals and the mean value was used for analysis.
May 1, 2024- January 1, 2025

Collaborators and Investigators

This is where you will find people and organizations involved with this 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 1, 2024

Primary Completion (Actual)

January 1, 2025

Study Completion (Actual)

January 1, 2025

Study Registration Dates

First Submitted

February 8, 2025

First Submitted That Met QC Criteria

February 12, 2025

First Posted (Actual)

March 25, 2025

Study Record Updates

Last Update Posted (Actual)

March 25, 2025

Last Update Submitted That Met QC Criteria

February 12, 2025

Last Verified

February 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • 2024-114

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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