- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06799663
Comparison the Effect of Smart Phones Addiction Between Children and Adolescents on Posture Deviations , Physical Fitness and Intelligence in Egypt
February 20, 2025 updated by: Ahmed Magdy EL-assar, Kafrelsheikh University
Comparison the effect of smart phones addiction between children and Adolescents on posture deviations , physical fitness and intelligence in Egypt
Study Overview
Status
Recruiting
Conditions
Study Type
Observational
Enrollment (Estimated)
60
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: Ahmed Magdy Elassar, Master
- Phone Number: 01023472407
- Email: Ahmedelassar67@gmail.com
Study Locations
-
-
-
Kafrelsheikh, Egypt
- Recruiting
- Kafrelsheikh University
-
Contact:
- Abdelrazek Youssef Desouky, Prof
- Phone Number: 002-047-3109590
- Email: President@kfs.edu.eg
-
-
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
No
Sampling Method
Non-Probability Sample
Study Population
Children and adolescents from 9 years to 18 years
Description
Inclusion Criteria:
- Subjects with the following criteria will be enrolled in this study :
The participants will be from middle childhood to adolescents and their age will be ranged from 9to 18 years.
They had Body Mass Index (BMI) = 18.5 :40 . They have a score of 24 or more on the Smart phones addiction scale-short version.
Exclusion Criteria:
- Subjects will be excluded from the study if the participant has the followings that affect that study:
visual or hearing defects, cachexia, any neurological disorders and musculoskeletal problems, any congenital abnormalities .
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 |
|---|---|
|
Children
|
Physical activity questionnaire will be applied on children and adolescents to compare the effect of smart phone on physical fitness
Raven's Progressive Matrices test will be applied on children and adolescents to compare the effect of smart phone on intelligence
Postural assessment software will be applied on children and adolescents to compare the effect of smart phone on posture
|
|
Adolescents
|
Physical activity questionnaire will be applied on children and adolescents to compare the effect of smart phone on physical fitness
Raven's Progressive Matrices test will be applied on children and adolescents to compare the effect of smart phone on intelligence
Postural assessment software will be applied on children and adolescents to compare the effect of smart phone on posture
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Physical fitness
Time Frame: 2 months
|
2 months
|
|
Postural deviation on head and neck
Time Frame: 3 months
|
3 months
|
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)
April 1, 2025
Primary Completion (Estimated)
October 1, 2025
Study Completion (Estimated)
February 1, 2026
Study Registration Dates
First Submitted
January 23, 2025
First Submitted That Met QC Criteria
January 23, 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 20, 2025
Last Verified
February 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- KFSIRB200-358
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
IPD Plan Description
The data will be shared upon the reasonable request from the principal investigator
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- SAP
- ICF
Drug and device information, study documents
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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