- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06446700
Correlation Between Neck Pain and Visual Disturbances in Smartphone Users
Study Overview
Status
Conditions
Intervention / Treatment
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
Enrollment (Actual)
Contacts and Locations
Study Locations
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Cairo, Egypt
- Yasmin Saeed Atallah
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Sampling Method
Study 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
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
Sponsor
Investigators
- Study Director: Mohamed H Elgendy, PROFESSOR
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
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)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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