Effect of Use Smartphone in Forward Head Position and Neutral Position on Upper Limbs Nerves

November 20, 2020 updated by: Karim Samy Ibrahim, MTI University

Electrophysiological Studies Of Induced Forward Head Position And Hand Use Of Mobile Phone

To compare between two different positions (forward head position and neutral position) when using mobile phone by hand using nerve conduction velocity and F-wave of upper limb nerves ( ulnar, median and radial) in 4 different times.

Study Overview

Status

Unknown

Conditions

Intervention / Treatment

Detailed Description

PURPOSE:

  • To compare between forward head position and hand use of mobile phone on conduction velocity of upper limb nerves
  • To investigate the F responses of upper limbs nerves.
  • To investigate the compound muscle action potential (CMAP) amplitudes of median nerves

BACKGROUND:

Forward head position may affect the cervical nerve root so it can also affect nerve conduction velocity due to continues stretch on nerves, also the over use of smart phone by hand may be affected the hand nerves, so this study determine which one of them has more influence than the other.

If the forward head position has the worst effect on the upper limb nerves investigators must avoid the incorrect position of the head to avoid stretch and compression of the nerves.

HYPOTHESES:

There are no statistical difference between forward head position and hand use of mobile phone on conduction velocity of the nerves of upper limb.

SUBJECTS:

Normal one hundred fifty non-athketic adolescents of both genders will participate in this study. Their age ranges from 14-18 years.

METHODS FOR ASSESSMENT

  1. Electromyography (EMG) will be used to measure nerve conduction velocity, F-wave, motor action potential
  2. Soft collar will used to fixed the craniovertebral angle during used mobile phone Universal goniometer
  3. Goniometer pro iPhone application

Study Type

Observational

Enrollment (Anticipated)

150

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 Locations

      • Cairo, Egypt
        • Recruiting
        • Faculty of Pysical Therapy, 6 Oct 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

14 years to 18 years (Child, Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

normal subjects

Description

Inclusion Criteria:

  1. Their ages range from 14-18 years.
  2. Not rolled on any regular athletic activity

Exclusion Criteria:

  1. Individual with neck pain
  2. Congenital deformity for upper limb
  3. Peripheral neuropathy due to diabetes mellitus type I
  4. Rheumatoid arthritis
  5. History of surgical intervention at nerves of the upper extremity

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
forward head position
nerve conduction velocity and f-wave applied to median , ulnar and radial nerve before and after 10,20 and 30 minutes in forward head position while Children will sit on chair with their feet on the ground without any tension, the upper limbs are rested in a table then, the angle between the line passing horizontally from the spinous process of C7 and the line passing between the tragus and spinous process of C7 will be measured by goniometer and goniometer pro application to evaluate the craniovertebral angle recording, we will fix the craniovertebral angle between 40.7° and 43.2°(severe FHP )
Samsung A 71
Other Names:
  • mobile phone
neutral position
nerve conduction velocity and f-wave applied to median , ulnar and radial nerve before and after 10,20 and 30 minutes while Children will sit on chair with their feet on the ground with head in anatomical position, the upper are rested in a table and used both hand on touch screen of mobile phone
Samsung A 71
Other Names:
  • mobile phone

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
motor and sensory nerve conduction velocity and f-wave in neutral position
Time Frame: 1 day
motor and sensory nerve conduction velocity and f-wave will measured to nerves of upper extremities ( median, ulnar and radial nerves) in neutral position by using electrodiagnosis when using mobile phone
1 day

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
motor and sensory nerve conduction velocity and f-wave measured in forward head position during use mobile phone
Time Frame: 1 day
motor and sensory nerve conduction velocity and f-wave will measured to nerves of upper extremities ( median, ulnar and radial nerves) in forward head position by using electrodiagnosis when using mobile phone
1 day

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)

February 10, 2020

Primary Completion (Anticipated)

February 10, 2021

Study Completion (Anticipated)

March 10, 2021

Study Registration Dates

First Submitted

September 14, 2020

First Submitted That Met QC Criteria

November 20, 2020

First Posted (Actual)

December 1, 2020

Study Record Updates

Last Update Posted (Actual)

December 1, 2020

Last Update Submitted That Met QC Criteria

November 20, 2020

Last Verified

November 1, 2020

More Information

Terms related to this study

Other Study ID Numbers

  • 012/002542

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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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