- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05483361
Effect Of Smart Phone Addiction On Pulmonary Function, And Functional Capacity In Children
Statement of the problem:
Are there relations between smartphone addiction, neck posture, pulmonary functions and functional capacity in children? Null hypothesis
It will be assumed that:
- There will be no effect of smart phone addiction on head posture, pulmonary function and functional capacity in children.
- There will be no relation between smartphone addiction, head posture, pulmonary function and functional capacity in children.
Study Overview
Status
Detailed Description
Subjects:
Sample size estimation will be carried out to determine the recruited number of children selected randomly from both governmental and private primary and preparatory schools at El Mansoura educational administration, Dakahlia Governorate and Damietta governorate to participate in this study. The survey targets the normal students from both sexes.
They will be selected based on the following:
Inclusion criteria:
- All children will be age ranges from 10 to 12 years
- The BMI <95th percentile (WHO, 2007)
- Smartphone addiction scale short version will be used to categorize the children to addicted group (score > 32) (Kwon et al., 2013) .
- They will be cooperative and followed the instructions.
Exclusive criteria:
Children will be excluded from the study if they have:
- Neurological diseases.
- Respiratory disorders.
- Congenital deformities.
- Vision disorders not corrected by glasses.
- Children who participate in competitive sports.
- Obesity.
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Contact
- Name: yasmine eletreby
- Phone Number: +201554984342
- Email: yeletreby@horus.edu.eg
Study Locations
-
-
-
Damietta, Egypt
- Recruiting
- Governmental and Private Primary and Preparatory Schools
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- All children will be age ranges from 10 to 12 years
- The BMI <95th percentile (WHO, 2007)
- Smartphone addiction scale short version will be used to categorize the children to addicted group (score > 32) (Kwon et al., 2013) .
- They will be cooperative and followed the instructions.
Exclusion Criteria:
• Neurological diseases.
- Respiratory disorders.
- Congenital deformities.
- Vision disorders not corrected by glasses.
- Children who participate in competitive sports.
- Obesity.
Study Plan
How is the study designed?
Design Details
- Observational Models: Other
- Time Perspectives: Cross-Sectional
Cohorts and Interventions
Group / Cohort |
|---|
|
smart phone addiction group
Smart phone addiction will be assessed using the Smart Phone Addiction Scale short version (SAS-SV) evaluation of pulmonary functions and functional capacity evaluation craniovertebral angle
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
evaluation of pulmonary functions
Time Frame: baseline only
|
Computerized spirometer is the most frequently used measure of lung function and is a measure of volume against time.
It is a simple and quick procedure to perform
|
baseline only
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
evaluation of functional capacity
Time Frame: baseline only
|
By 3 minutes step test It is based on the principles that your heart rate will return to normal quickly the fitter you are the value of post- exercise heart is considered to be an indicator to cardiovascular fitness
|
baseline only
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
evaluation craniovertebral angle
Time Frame: baseline only
|
By Kinovea computer program A free 2D motion analysis software
|
baseline only
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: yasmine eletreby, Cairo university
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- P.T.REC/012/003600
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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