Correlation Between Smartphone Addiction and Back Dysfunction and Core Muscle Morphology and Performance in Asymptomatic Young Adults

April 2, 2022 updated by: Asmaa Mahmoud Hussin, Cairo University
The purpose of this study is to investigate the association between smartphone addiction and back pain, function, and lumbar stabilizer cross-sectional area and thickness compared with non-addicted teenagers.

Study Overview

Status

Not yet recruiting

Detailed Description

Smartphone prolonged use has been suggested as a risk factor for psychological, visual, and musculoskeletal dysfunctions. The musculoskeletal dysfunction may be related to direct contact use with smartphones as in thumb, elbow, and neck pain. Moreover, indirect long use of smartphones may affect thoracic, lumbar, and lower limbs.

COVID-19 pandemic occurred in a time of outstanding scientific progress and global digitalization. Therefore, smartphone usage became a must for human connection, learning, and entertainment, providing psychological and social support. In the meantime, it was observed a significant increase in overuse and addiction, especially in young and teenage females. The addiction is associated with more musculoskeletal abnormalities when compared to non-addict users. Several studies found an association between smartphone usage and back pain, concomitant with a reduction in thoracic extensors activity. This back pain may affect their quality of life and work-related productivity. However, the relationship between back dysfunction and smartphone addiction is still unclear. A few attempts were done to elucidate this relationship. Yet if proven correct, then preventive measures such as recommendations and precautions regarding smartphone use could be distributed to users by the manufacturers. Furthermore, engineering solutions are needed to optimally design smartphones to alter their weight and sizes to minimize potential adverse effects.

Study Type

Observational

Enrollment (Anticipated)

136

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

      • Dokki, Egypt, 34518
        • outpatient clinic, faculty of physical therapy, Cairo 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

18 years to 30 years (Adult)

Accepts Healthy Volunteers

N/A

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

Using G-power version 3.1.9.7 for windows and regarding T-test study, alpha level of 0.05, confidence interval 95% and effect size of 0.25 (to detect small effects), two groups and six dependent variables, the total sample size was 136 subjects.

Description

Inclusion Criteria:

  1. Age ranged from 18 years to 30 years.
  2. BMI between 19.0-29.9 kg/m2.

Exclusion Criteria:

1- Previous history of spinal trauma or dysfunction. 2 - Any systemic disease that may affect spine such as ankylosing spondylitis and rheumatoid arthritis.

3 - Cognitive or memory impairment in memory or cognitive function.

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
Smartphone addict
Smartphone non addict

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Assessment of back function and disability
Time Frame: at baseline only
Functional disability will be assessed by the Oswestry disability questionnaire, a functional scale assessing the impact of LBP on daily activities. It is a self-administered, 10-item questionnaire: the first section rates the intensity of pain and the others describe its disabling effect on typical daily activities. The score for each item ranges from 0 to 5, the score is calculated by the addition of the values assigned for each of the 10 individual questions
at baseline only
Musculoskeletal assessment By Ultrasonography
Time Frame: at baseline only
Ultrasonography will be used for measuring CSA and MT of LMM. Muscle thickness measurement by US.
at baseline only
Core muscles strength
Time Frame: at baseline only
Core stability will be measured using prone and supine bridging as bridging maneuvers seem to be practical, reliable, and valid methods of reflecting lumbar spine stabilization endurance capability. In prone bridge each subject will be in the prone position, supporting on the elbows. The elbows will be spaced shoulder-width apart, and the feet were set with a narrow base, but not touching. The subject then asked to raise the pelvis from the floor so that only the forearms and the toes were in contact with the floor. The shoulders, hips, and ankles were maintained in a straight line.
at baseline only

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 (Anticipated)

April 1, 2022

Primary Completion (Anticipated)

June 1, 2022

Study Completion (Anticipated)

June 15, 2022

Study Registration Dates

First Submitted

March 19, 2022

First Submitted That Met QC Criteria

April 2, 2022

First Posted (Actual)

April 11, 2022

Study Record Updates

Last Update Posted (Actual)

April 11, 2022

Last Update Submitted That Met QC Criteria

April 2, 2022

Last Verified

April 1, 2022

More Information

Terms related to this study

Other Study ID Numbers

  • Asmaa_PhD_2022

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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