- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05260632
Effect of Smartphone Addiction on Manual Coordination, Strength and Hand Pain in Normal Teenage Students
Statement of the problem:
• Does addiction of smart phone affect upper limb coordination, manual dexterity, hand grip and pinch strength?
Null Hypotheses:
• Addiction of smart phone does not affect upper limb coordination, manual dexterity, hand grip and pinch strength in normal teenage students.
Study Overview
Status
Detailed Description
Subjects:
The survey targets the normal teenage students from both sexes. Sample size estimation will be carried out to determine the recruited number of students, selected randomly from both governmental and private preparatory and secondary schools at Ashmoon educational administration, Menofia Governorate to participate in this study.
Study design:
Cross sectional observational study. Sample design will be a cluster sample,
A. Inclusion criteria:
- The students' age will range from 12 to 18 years.
- Normal students including both boys and girls.
- Participants have a range score from 31 to 60 points for boys and from 33 to 60 points for girls on smartphone addiction scale according to Kwon et al (2013).
- Their body mass index will be within the normal range according to WHO indices .
- Cooperative students who wish to participate in the current study.
- The students will represent different socioeconomic levels.
B. Exclusion criteria:
The students will be excluded from the study if they have one of the following:
- Congenital abnormalities or medical conditions, which may affect the study.
- Musculoskeletal problems such as previous or recent orthopedic surgery, fractures, prostheses, inflammation of the fingers, arms, or shoulder.
- Visual or hearing defects.
- Motor, behavioral, or neurologic disorders and learning disabilities. • Participants have a range score from 31 to 60 points for boys and from 33 to 60 points for girls on smartphone addiction scale, then participants will be divided into 2 levels of addiction.
Assessment of manual dexterity and upper extremity coordination will be carried out by using The Bruininks-Oseretsky Test of Motor Proficiency, Second Edition (BOT-2) (Bruininks and Bruininks, 2005). Hand grip strength and pinch strength will be assessed by hand dynamometer and pinch meter.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Cairo, Egypt, 34518
- outpatient clinic, faculty of physical therapy, Cairo university
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- The students' age will range from 12 to 18 years.
- Normal students including both boys and girls.
- Participants have a range score from 31 to 60 points for boys and from 33 to 60 points for girls on smartphone addiction scale according to Kwon et al (2013).
- Their body mass index will be within the normal range according to WHO indices .
- Cooperative students who wish to participate in the current study.
- The students will represent different socioeconomic levels.
Exclusion Criteria:
The students will be excluded from the study if they have one of the following:
- Congenital abnormalities or medical conditions, which may affect the study.
- Musculoskeletal problems such as previous or recent orthopedic surgery, fractures, prostheses, inflammation of the fingers, arms, or shoulder.
- Visual or hearing defects.
Motor, behavioral, or neurologic disorders and learning disabilities
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Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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no intervention
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2 groups
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Assessment of Manual coordination
Time Frame: Baseline - one hour for each participant
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Assessment of change in manual dexterity and upper extremity coordination will be carried out by using The Bruininks-Oseretsky Test of Motor Proficiency, Second Edition (BOT-2) (Bruininks and Bruininks, 2005).
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Baseline - one hour for each participant
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Assessment of hand grip strength
Time Frame: Baseline - one hour for each participant
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Assessment of change in Hand grip strength will be assessed by hand dynamometer device.
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Baseline - one hour for each participant
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Assessment of pinch strength
Time Frame: Baseline - one hour for each participant
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Assessment of change in pinch strength by pinchmeter device.
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Baseline - one hour for each participant
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Amira Mohamed, Cairo University
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ACTUAL)
Study Completion (ACTUAL)
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/012/003440
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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