Screen Culture's Impact on Generation Z Adolescents' Physical Activity, Posture and Well-being in Egypt

April 30, 2026 updated by: Alaa Noureldeen Kora, Sinai University

Screen Culture's Impact on Generation Z Adolescents' Physical Activity, Posture and Well-being in Egypt: A Cross-sectional Study

Ubiquitous adoption of screen-based technologies has transformed the behavioral and physiological environment of Generation Z youth. In Egypt, where digital adoption speeds up with apace urbanisation, teens (13-18) have greater exposure to computers, mobile phones, and other screen-based devices.

Growing evidence points towards excessive viewing of screens in compromised well-being, including sleep issues, inactive lifestyles, weight loss/gain, and musculoskeletal disturbances. Contextual evidence for the Egyptian teenager is scarce.

This study fills the gap by investigating the multi-dimensional influence of screen culture on physical well-being, focusing on sleep quality, body mass index (BMI), posture, physical activity, and disability outcomes.

Study Overview

Study Type

Observational

Enrollment (Actual)

532

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

      • Ismailia, Egypt, 11749
        • Sinai 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

  • Child
  • Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Probability Sample

Study Population

Generation Z Adolescences (Age 13 to 18)

Description

Inclusion Criteria:

  • Age: 13-18 years (adolescence as per WHO standards).
  • Nationality: Egyptian residents.
  • Language Proficiency: Ability to read and comprehend English (the questionnaires are in English).
  • Screen Use: ≥1 screen device used frequently (e.g., smartphone, laptop, tablet).

Exclusion Criteria:

  • Can not o read and comprehend English language Do not have a routine of a screen time

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
Adolesence

Age: 13-18 years (adolescence as per WHO standards).

  • Nationality: Egyptian residents.
  • Language Proficiency: Ability to read and comprehend English (the questionnaires are in English).
BMI Measurement: Self-report height/weight (compared with age/sex standard BMI percentiles).
Screen Time Questionnaire (QUEST): Assess length, purpose, and pattern of device use.
Insomnia Severity Index (ISI): 7-item sleep disturbance severity measure (score range: 0-28).
Q-BAPHYP: 20-item scale measuring body awareness, postural habits, and ergonomic behaviors.
PedsQL™: Pediatric Quality of Life Inventory

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
sleep disturbance severity
Time Frame: 1 day

Scale Used: Insomnia Severity Index (ISI)

Description:

The ISI is a 7-item self-report questionnaire that assesses the severity of insomnia and its impact on daily functioning. Each item is scored on a 0-4 scale, with total scores ranging from 0 to 28. Higher scores indicate more severe sleep disturbance.

1 day
body awareness
Time Frame: 1 Day

Scale Used: Q-BAPHYP

Description:

The body awareness component of the Q-BAPHYP scale assesses an individual's awareness of their body position, movement, and physical sensations. It may include items related to:

Recognition of poor posture

Awareness of physical discomfort during screen use

Sensitivity to bodily signals (e.g., fatigue, muscle tension)

Attention to ergonomic positioning

1 Day
Pediatric Quality of Life
Time Frame: 1 Day

Scale Used: PedsQL™ (Pediatric Quality of Life Inventory)

Description:

The PedsQL™ is a modular instrument designed to measure health-related quality of life in children and adolescents. It covers multiple dimensions of well-being across:

Physical Functioning (e.g., ability to engage in physical activities)

Emotional Functioning (e.g., feeling anxious or sad)

Social Functioning (e.g., interactions with peers)

School Functioning (e.g., ability to concentrate and attend school)

1 Day

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Postural Habits
Time Frame: 1 Day
The body awareness component of the Q-BAPHYP scale assesses an individual's awareness of their body position, movement, and physical sensations
1 Day

Collaborators and Investigators

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

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)

July 15, 2025

Primary Completion (Actual)

January 1, 2026

Study Completion (Actual)

January 30, 2026

Study Registration Dates

First Submitted

November 14, 2025

First Submitted That Met QC Criteria

November 20, 2025

First Posted (Actual)

November 25, 2025

Study Record Updates

Last Update Posted (Actual)

May 4, 2026

Last Update Submitted That Met QC Criteria

April 30, 2026

Last Verified

April 1, 2026

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • SU.REC.2025 (57 H)

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

IPD Plan Description

According to the data confidentiality

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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