- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05321030
Correlation Between Smartphone Addiction and Back Dysfunction and Core Muscle Morphology and Performance in Asymptomatic Young Adults
Study Overview
Status
Conditions
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
Enrollment (Anticipated)
Contacts and Locations
Study Locations
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Dokki, 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:
- Age ranged from 18 years to 30 years.
- 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
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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Smartphone addict
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Smartphone non addict
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Assessment of back function and disability
Time Frame: at baseline only
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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
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at baseline only
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Musculoskeletal assessment By Ultrasonography
Time Frame: at baseline only
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Ultrasonography will be used for measuring CSA and MT of LMM.
Muscle thickness measurement by US.
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at baseline only
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Core muscles strength
Time Frame: at baseline only
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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.
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at baseline only
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Anticipated)
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
- Asmaa_PhD_2022
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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