NCT06446700

Brief Summary

the goal of this study is to Investigate the correlation between neck pain and visual disturbances in smartphone users.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
141

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Apr 2024

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

April 1, 2024

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

May 23, 2024

Completed
2 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 25, 2024

Completed
7 days until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2024

Completed
5 days until next milestone

First Posted

Study publicly available on registry

June 6, 2024

Completed
Last Updated

June 6, 2024

Status Verified

June 1, 2024

Enrollment Period

2 months

First QC Date

May 23, 2024

Last Update Submit

June 1, 2024

Conditions

Keywords

neck painvisionsmartphone

Outcome Measures

Primary Outcomes (2)

  • Neck disability index

    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

    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

Interventions

participants complete the 2 questionnaire by an online form and paper

Also known as: visual functional questionnaire

Eligibility Criteria

Age18 Years - 50 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)
Sampling MethodNon-Probability Sample
Study Population

participants from universities and local population

You may qualify if:

  • 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

You may not qualify if:

  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Yasmin Saeed Atallah

Cairo, Egypt

Location

MeSH Terms

Conditions

Neck Pain

Condition Hierarchy (Ancestors)

PainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • Mohamed H Elgendy

    Professor

    STUDY DIRECTOR

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal investigator

Study Record Dates

First Submitted

May 23, 2024

First Posted

June 6, 2024

Study Start

April 1, 2024

Primary Completion

May 25, 2024

Study Completion

June 1, 2024

Last Updated

June 6, 2024

Record last verified: 2024-06

Data Sharing

IPD Sharing
Will not share

Locations