- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06497257
Effect of Smartphone Overuse on Hand Strength and Function in Physical Therapy Students
Study Overview
Status
Conditions
Detailed Description
Smartphones have become ubiquitous worldwide, offering significant potential for medical applications by providing healthcare professionals and students with instant access to resources for informed decision-making. However, despite their benefits, overuse of smartphones can lead to physical health issues. Grip strength is recognized as an indicator of overall muscle strength, upper limb function, and various health conditions. Isokinetic testing, a reliable method for measuring muscle performance, has been widely used in studying low back pain but less commonly applied to wrist strength assessment.
Currently, there is a lack of evidence regarding the impact of smartphone overuse on wrist flexor and extensor peak torque, handgrip strength, and function. This research aims to investigate these aspects, providing insights into upper extremity function and potentially aiding ergonomists in addressing musculoskeletal disorders. The study's findings could contribute to the biomechanical evaluation and design of upper extremity tasks, enhance understanding of wrist functioning, and inform ergonomic design considerations. Additionally, the results may help smartphone users adopt better postures and grasping techniques to minimize injuries and maintain hand function, ultimately improving their quality of life.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
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Cairo, Egypt
- Nouran Mohamed Saad
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Age of subjects 18 to 25 years.
- Body mass index from 18, but less than 25 kg/m2.
- Experimental group, healthy subjects who are smartphone users for at least two years prior to study.
Exclusion Criteria:
- Subjects with a history of neurological disorder affecting the upper extremities, vestibular dysfunction, or balance disorder.
- Deformities of elbow or hand.
- Any recent upper limb fracture or trauma.
- Disorders like carpal tunnel syndrome, radiculopathy or tendinopathy.
- Individuals going to the gym or athletes.
- Individuals who smoke.
- Subjects who had cognitive, linguistic or vision impairment which limited their use of instruments and questionnaire.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Group of high-frequency smartphone users
Male and female subjects, who are high-frequency smartphone users at least for two years before the study.
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Evaluation of wrist flexor and extensor peak torque
Evaluation of functional disability
Evaluation of hand grip strength
|
|
Group of low-frequency smartphone users
Male and female subjects, who are low-frequency smartphone users.
|
Evaluation of wrist flexor and extensor peak torque
Evaluation of functional disability
Evaluation of hand grip strength
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Measurement of wrist flexor peak torque
Time Frame: 1 month
|
It will be measured by the Biodex system 3 pro isokinetic dynamometer.
|
1 month
|
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Measurement of wrist extensor peak torque
Time Frame: 1 month
|
It will be measured by the Biodex system 3 pro isokinetic dynamometer.
|
1 month
|
|
Assessment of functional disability
Time Frame: 1 month
|
It will be assessed by the patient-related wrist and hand evaluation (PRWHE) questionnaire.
|
1 month
|
|
Measurement of hand grip strength
Time Frame: 1 month
|
It will be measured by a JAMAR Handheld Dynamometer.
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1 month
|
Collaborators and Investigators
Sponsor
Investigators
- Study Chair: Hanaa Kenawy, PhD, Faculty of physical therapy, Cairo University, Giza, Egypt.
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/012/005125
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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