Correlation Between Neck Pain and Visual Disturbances in Smartphone Users

June 1, 2024 updated by: Yasmin Saeed Atallah, Cairo University
the goal of this study is to Investigate the correlation between neck pain and visual disturbances in smartphone users.

Study Overview

Detailed Description

Study design:

Cross-sectional observational analytical study design conducted on smartphone users 2- Subject selection 141 subjects (who are smartphone users) according to sample size calculation will be selected randomly to complete the neck disability index and visual functional questionnaire 25 version 2000

Study Type

Observational

Enrollment (Actual)

141

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

      • Cairo, Egypt
        • Yasmin Saeed Atallah

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

participants from universities and local population

Description

Inclusion Criteria:

  • 141 subjects who are smartphone users
  • Age between 18 to 50 years
  • Both genders are included
  • Subjects Who put in more than 4 hours a day using smartphone
  • Participants without systemic illnesses or physical deformities were also included
  • Consent: Participants who provide informed consent to participate in the study.
  • Neck disability index will be used to assess how your neck pain has affected your ability to manage in everyday life.
  • Visual Functioning Questionnaire version 2000 will be used to assess vision-related quality of life

Exclusion Criteria:

  • People with head and neck injuries
  • eye diseases
  • People with diabetic retinopathy
  • who had refractive correction surgery
  • psychiatric problems (depression)
  • people with systemic illnesses or physical deformities
  • people who have vision impairments and disabilities

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
Neck disability index
Time Frame: 1 month

Patient-completed, condition-specific functional status questionnaire with 10 items including pain, personal care, lifting, reading, headaches, concentration, work, driving, sleeping and recreation.

This questionnaire has been designed to give us information as to how your neck pain has affected your ability to manage in everyday life.

The NDI can be scored as a raw score or doubled and expressed as a percent. Each section is scored on a 0 to 5 rating scale, in which zero means 'No pain' and 5 means 'Worst imaginable pain'.

Points summed to a total score. The test can be interpreted as a raw score, with a maximum score of 50, or as a percentage.

0 points or 0% means: no activity limitations, 50 points or 100% means complete activity limitation. A higher score indicates more patient-rated disability.

1 month
Visual functional questionnare
Time Frame: 1 month
The VFQ-25 consists of a base set of 25 vision targeted questions representing 11 vision-related constructs, plus an additional single-item general health rating question The VFQ-25 takes approximately 10 minutes on average to administer in the interviewer format. There is also a self-administered version of theSurvey.
1 month

Collaborators and Investigators

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

Investigators

  • Study Director: Mohamed H Elgendy, PROFESSOR

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)

April 1, 2024

Primary Completion (Actual)

May 25, 2024

Study Completion (Actual)

June 1, 2024

Study Registration Dates

First Submitted

May 23, 2024

First Submitted That Met QC Criteria

June 1, 2024

First Posted (Actual)

June 6, 2024

Study Record Updates

Last Update Posted (Actual)

June 6, 2024

Last Update Submitted That Met QC Criteria

June 1, 2024

Last Verified

June 1, 2024

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • neck pain and vision

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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