- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05817877
Investigation of the Relationship of Smartphone Use Time With Neck Endurance, Head Posture, Lateral Grip Strength, Hand Grip Strength and Postural Control Parameters in Young Adults
September 5, 2023 updated by: Zeynep SAG, Dokuz Eylul University
In the planned study, young adults between the ages of 18-35 with different phone usage durations will be evaluated.
The aim of the study is to investigate whether the average daily phone usage time has a direct relationship with neck muscle endurance, rough grip strength, lateral grip strength and head posture, and whether there is an indirect relationship with postural control.
People who have phones with IOS 12 or Android 9 and above will be invited to the study.
By looking at the screen time tracking feature in these versions, the daily phone usage hour for the last week will be calculated and the participants will be divided into two groups as the daily phone usage average of 5, and below and 5 hours.
In the planned study, neck endurance will be tested on flexor and extensor muscle groups in accordance with the literature.
The lateral flexion and anterior tilt angles will be calculated with two photographs taken from the anterior and lateral sides of the head posture of the person's shoulder, and the hand grip strength will be measured with a Jamar hand dynamometer and the lateral grip strength will be measured with a pinchmeter.
Postural control evaluation will be measured by means of center of pressure-CoP parameters measured with TekScan brand pressure platform.
The study is planned to be carried out in the Movement Analysis Laboratory of the Faculty of Physical Therapy and Rehabilitation of Dokuz Eylul University.
Participants will be selected from healthy adults between the ages of 18-35 who volunteered to participate in the study among the students of the Faculty of Physical Therapy and Rehabilitation, their relatives and the relatives of the researcher.
The study is planned to be completed within 6 months following ethical approval.
Study Overview
Study Type
Observational
Enrollment (Estimated)
120
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Zeynep SAĞ
- Phone Number: +905065829407
- Email: fzt.zeynep.sag@gmail.com
Study Locations
-
-
Balçova
-
İzmir, Balçova, Turkey, 35330
- Recruiting
- Dokuz Eylül Univercity
-
Contact:
- İbrahim Engin Şimşek, Professor
- Phone Number: +905323476148
- Email: iengin.simsek@gmail.com
-
-
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
Yes
Sampling Method
Probability Sample
Study Population
healthy young adults
Description
Inclusion Criteria:
- Using a phone with IOS 12 or android 9 and above for at least one week
Exclusion Criteria:
- Presence of orthopedic surgery in the last 6 months
- Those who have a disease or take medication that will prevent neuromuscular system and postural control measurements
- have neck pain
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
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
over 5 hours
people with an average daily phone use of more than 5 hours.
|
There is no intervention.
|
|
under 5 hours
People with an average daily phone use of less than 5 hours.
|
There is no intervention.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
postural control parameters
Time Frame: up to 8 weeks
|
Postural control can be quantitatively assessed by examining the behavior of the statically or dynamically in the lower pressure center (CoP).
|
up to 8 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
hand grip strength
Time Frame: up to 8 weeks
|
hand grip is the numerical output of the brute grip strength of the hand
|
up to 8 weeks
|
|
lateral grip strength
Time Frame: up to 8 weeks
|
The lateral grip is a numerical measurement of the maximum strength of the thumb abductor muscles, which we do not use especially during texting.
|
up to 8 weeks
|
|
neck muscle endurance
Time Frame: up to 8 weeks
|
neck muscle endurance is the numerical data of the endurance of the neck flexor and extensor muscles
|
up to 8 weeks
|
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)
March 14, 2023
Primary Completion (Actual)
June 20, 2023
Study Completion (Estimated)
March 14, 2024
Study Registration Dates
First Submitted
March 23, 2023
First Submitted That Met QC Criteria
April 5, 2023
First Posted (Actual)
April 18, 2023
Study Record Updates
Last Update Posted (Actual)
September 7, 2023
Last Update Submitted That Met QC Criteria
September 5, 2023
Last Verified
September 1, 2023
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 2023/03-14
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
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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