- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07055815
- Original Trial
Impact of Digital Screen Time in Progression of Myopia in Children
June 28, 2025 updated by: Muhammad Naveed Babur, Superior University
Research suggests that prolonged digital screen time is a significant contributing factor to the progression of myopia in children.
Studies have shown that increased near-work activities, such as reading, writing, and screen time, can lead to an increased risk of developing myopia.
The widespread use of digital devices among children has raised concerns about the potential impact on their eye health.
Study Overview
Status
Active, not recruiting
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Actual)
79
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
-
-
Punjab
-
Lahore, Punjab, Pakistan
- Watan optical
-
-
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
- Child
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
Impact of Digital Screen Time in Progression of Myopia in Children he widespread use of digital devices among children has raised concerns about the potential impact on their eye health.
Excessive screen time can cause prolonged near focus, reduced outdoor time, and increased blue light exposure, all of which may contribute to myopia progression.
Description
Inclusion Criteria:
- Both male and female myopic children of age 6 to 12 years were included with BCVA 6/6 with no any eye pathology.
- No medication or disease that could affect vision.
- Spherical equivalent of cylinder 0.50 to 1.00 were added.
Exclusion Criteria:
- Opacity, cataract, any fundus pathologies, strabismus or indication of previous ocular surgeries were excluded.
- High astigmatic children were excluded or more than 1.00DC.
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 |
|---|---|---|
|
self admistred questioner
Time Frame: 12 Months
|
self admistred questioner to check Mild, moderate, and severe Myopia in Children
|
12 Months
|
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)
March 17, 2025
Primary Completion (Estimated)
September 1, 2025
Study Completion (Estimated)
February 28, 2026
Study Registration Dates
First Submitted
June 28, 2025
First Submitted That Met QC Criteria
June 28, 2025
First Posted (Actual)
July 9, 2025
Study Record Updates
Last Update Posted (Actual)
July 9, 2025
Last Update Submitted That Met QC Criteria
June 28, 2025
Last Verified
June 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- MSRSW/Batch-Fall23/831
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.
Clinical Trials on Myopia, Progressive
-
Zhongshan Ophthalmic Center, Sun Yat-sen UniversityGuangzhou Youyan Vision Technology Co., Ltd.Not yet recruiting
-
Shanghai General Hospital, Shanghai Jiao Tong University...Not yet recruitingMyopia | Myopia, ProgressiveChina
-
University of FaisalabadCompletedRefractive Errors | Myopia | Progressive MyopiaPakistan
-
Beijing Airdoc Technology Co., Ltd.Recruiting
-
Beijing Airdoc Technology Co., Ltd.The First People's Hospital of XuzhouRecruiting
-
Shanghai Eye Disease Prevention and Treatment CenterActive, not recruiting
-
Shanghai Eye Disease Prevention and Treatment CenterEnrolling by invitation
-
Universidad Complutense de MadridCooperativa de Ensino Superior, Politécnico e Universitário; Novovision; Instituto... and other collaboratorsActive, not recruiting
-
Nova Southeastern UniversityWithdrawnMyopia, Progressive
-
Tianjin Medical University Eye HospitalNot yet recruitingProgressive Myopia | Pediatric Myopia | Orthokeratology-related Myopia Progression
Clinical Trials on Progression of Myopia
-
The Hong Kong Polytechnic UniversityCompleted
-
Wang HongxiaTianjin Eye HospitalCompletedRefractive Error - Myopia AxialChina
-
Myoptechs, IncUniversity of Waterloo School of Optometry and Vision ScienceNot yet recruitingMyopia: Refractive Error
-
Indizen Optical Technologies, S.L.U.University of Minho; University of Ulster; Hospital San Carlos, MadridNot yet recruitingMyopia ProgressionSpain, Portugal, United Kingdom
-
Indizen Optical Technologies, S.L.U.Universidad Europea de MadridCompleted
-
Sun Yat-sen UniversityUnknownRefractive ErrorsChina
-
Essilor InternationalCompleted
-
Shanghai Eye Disease Prevention and Treatment CenterActive, not recruiting
-
Fangbiao TaoNot yet recruiting