- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06509035
Correlation Between Smartphone Use and Text Neck Posture in Asymptomatic Subjects
July 12, 2024 updated by: Hend Hesham Abd Elfatah Ali, Cairo University
This study will be conducted to investigate the correlation between the number of hours of smartphone usage and severity of text neck posture, cervical ROM, DNF endurance and resting head posture among asymptomatic 18 to 25 years old adults
Study Overview
Status
Completed
Conditions
Detailed Description
Smartphone use has increased significantly globally, with 79% of adults aged 18-44 carrying a smartphone constantly.
This can cause excessive anterior curves in the neck vertebrae and increase the mechanical load on cervical spine joints.
Overuse syndrome, spinal damage, and other side effects can result.
This study aims to investigate the correlation between time spent using smartphones and text neck posture and its association with head and neck posture, cervical ROM, and DNF endurance among asymptomatic 18-25-year-olds.
Study Type
Observational
Enrollment (Actual)
30
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
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Giza, Egypt
- Misr University for Science and Technology
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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
- Adult
Accepts Healthy Volunteers
N/A
Sampling Method
Probability Sample
Study Population
Thirty, males and females students, with age 18 - 25 years old recruited from faculty of physical therapy in Misr University for Science and Technology, 6 October, Egypt.
Description
Inclusion Criteria:
- Individuals who are willing to participate at the time of data collection.
- Individuals aged 18 - 25 years old.
- Individuals who use a smartphone to report the duration of weekly usage (at least one year of using a smartphone and minimum duration of smartphone use of ≥1 h per day
Exclusion Criteria:
- Previous history of an accident or severe injury.
- Any neurological or cardiovascular problem.
- Spinal surgery or any disease that prevents the individual from adopting an unsupported orthostatic posture.
- Congenital cervical problem.
- Pregnant women.
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Assessing the average duration of smartphone screen time
Time Frame: at baseline
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A mobile application called Screen Time Restrain Yourself measures smartphone usage in hours over the past week, allowing users to monitor their daily usage without disrupting normal smartphone use.
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at baseline
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Assessment of head and neck posture
Time Frame: at baseline
|
Photogrammetry is a reliable method for measuring head and cervical spine postures.
It involves taking sagittal photographs of the subject's head tilt angle and neck tilt angle.
A camera is positioned at a height corresponding to the seventh cervical vertebra (C7) level, and spherical markers are attached to the right tragus, canthus, and spinal process.
The subject is instructed to sit on a chair, maintain a resting head posture, and perform full flexion and extension three times.
The average of angles from repeated photos is used to reduce bias.
Fatigue time is reported after ten minutes of use with a smartphone.
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at baseline
|
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Assessment of cervical range of motion
Time Frame: at baseline
|
Cervical ROM is measured using a universal goniometer, with subjects placed flat on the floor and supported on a lap.
They move their head in flexion and extension, with the goniometer placed over the external auditory meatus, fixed arm perpendicular to the floor, and movable arm with the nose base.
For cervical rotation, they turn the head to the left or right side, and for lateral flexion, they touch the ear to a shoulder of the same side.
The goniometer is a valid and reliable tool for measuring cervical ROM, with good interrater and intraterrater reliability.
|
at baseline
|
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Assessment of deep neck flexor endurance
Time Frame: at baseline
|
The Neck Flexor Muscle Endurance Test (NFMET) involves a subject supine, with hands resting on the abdomen and feet flat on a plinth.
The subject performs chin retraction, head and neck lift, and skin folds.
The test measures muscle endurance, with males having a longer average hold time than females.
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at baseline
|
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 (Actual)
July 1, 2023
Primary Completion (Actual)
December 1, 2023
Study Completion (Actual)
June 1, 2024
Study Registration Dates
First Submitted
July 2, 2024
First Submitted That Met QC Criteria
July 12, 2024
First Posted (Actual)
July 19, 2024
Study Record Updates
Last Update Posted (Actual)
July 19, 2024
Last Update Submitted That Met QC Criteria
July 12, 2024
Last Verified
July 1, 2024
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- Hend PhD
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
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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