Smartphone Addiction and Isometric Strength of Rotator Cuff Muscles

October 7, 2024 updated by: Heba Abdallah Mohamed Bashier, Cairo University

Smartphone Addiction and Isometric Rotator Cuff Muscles Strength Among Adults

To investigate the relationship between smartphone addiction and isometric rotator cuff muscles strength among adults

Study Overview

Status

Recruiting

Conditions

Intervention / Treatment

Detailed Description

Smartphones play an important role in human life because they are used for communication, accessing the internet, and gaming. The rate of smartphone usage has increased over the last decade, as has the duration and frequency of use. according to one study, 79 percent of people aged 18 to 44 spent almost all of their time on their smartphones, with only two hours of the day spent without one.

No previous study has found a link between smartphone addiction and isometric Rotator Cuff muscular strength, to the authors' knowledge. Therefore, the primary purpose of this study will be to determine the relationship between smartphone addiction and isometric rotator cuff muscles strength.

Study Type

Observational

Enrollment (Estimated)

300

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

Study Contact Backup

Study Locations

      • Giza, Egypt, 12578
        • Recruiting
        • Outpatient clinic, faculty of Physical Therapy Cairo University

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

Non-Probability Sample

Study Population

1- This study will comprise 300 healthy volunteers between the ages of 18 and 30 who needed to use a smart phone

Description

Inclusion Criteria:

- 1- This study will comprise healthy volunteers between the ages of 18 and 30 who needed to use a smart phone.

2- Subjects who put in more than 4 hours per day using smartphone.

Exclusion Criteria:

  • Patients will rule out if

    1. They had any medical condition that could cause shoulder pain (such as impingement, subacromial bursitis, rotator cuff damage, or traumatic or degenerative supraspinatus tendonitis).
    2. Anyone with a positive Neer sign, a positive Hawkins sign, discomfort during shoulder elevation, pain at the location of the rotator cuff tendon, pain with resisted isometric shoulder abduction, or a history of pain in the C5 dermatome will be ruled out.
    3. Any individual who had previously suffered a musculoskeletal injury or surgery that could have influenced the measurement will be also eliminated.

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
isometric strength of rotator cuff
Time Frame: up to 3 month
Hand-held Dynamometer (HHD) is an ergonomic hand-held device used for objectively quantifying muscle strength.
up to 3 month

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

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, 2024

Primary Completion (Estimated)

October 30, 2024

Study Completion (Estimated)

November 30, 2024

Study Registration Dates

First Submitted

September 27, 2024

First Submitted That Met QC Criteria

October 7, 2024

First Posted (Estimated)

October 9, 2024

Study Record Updates

Last Update Posted (Estimated)

October 9, 2024

Last Update Submitted That Met QC Criteria

October 7, 2024

Last Verified

September 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • REC/PT/012/0167

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

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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