- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05377931
Ocular and Cardiac Effects of Battle Ground
May 12, 2022 updated by: Ahmed Abdelshafy, Benha University
Ocular and Cardiac Effects of Mobile Battle Ground Games
Mobile battle ground games are widely used in various age groups, there are ocular and cardiac affection that may affect users of this type of action games.
Study Overview
Status
Recruiting
Intervention / Treatment
Detailed Description
The aim of this study is to assess the possible ocular and cardiac changes that may affect users of this type of mobile games in real life among various age groups and especially in adults with history of recent corona virus (COVID-19) disease.
There is no medical recommendations about the time and the hazards of using this games for longer periods in real practice.
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
- Name: Ahmed Abdelshafy, MD
- Phone Number: 01222328766
- Email: ahmad4lg@gmail.com
Study Contact Backup
- Name: Marwa Abdelshafy, MD
- Phone Number: 01222328766
- Email: drmarwatabl2012@gmail.com
Study Locations
-
-
QA
-
Banhā, QA, Egypt, 13511
- Recruiting
- Ahmed Abdelshafy
-
Contact:
- Ahmed Abdelshafy, MD
- Phone Number: 01222328766
- Email: ahmad4lg@gmail.com
-
Contact:
- Marwa Abdelshafy, MD
- Phone Number: 01222328766
- Email: ahmad4lg@gmail.com
-
Sub-Investigator:
- Mohamed Abdelshafy, MD
-
-
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
18 years to 40 years (Adult)
Accepts Healthy Volunteers
N/A
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Subjects that are using action mobile games during their leisure and are members of faculty of medicine, Banha university and are seeking to participate in this study.
Description
Inclusion Criteria:
- Normal subjects that are playing or not playing action mobile battle ground games will be included.
- Post COVID-19 subjects with average 6 months of infection and are playing mobile battle. Ground games will be included.
Exclusion Criteria:
- Subjects that refuse to enter the study.
- Users of mobile battle ground games with other diseases that may affect ocular and cardiac assessment as diabetic eye disease, cardiac congenital anomalies or recent cardiac or ocular surgery.
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
- Observational Models: Cohort
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Normal subjects users of battle ground games (Group 1)
Subjects with no history of any medical diseases that are using mobile battle ground games for average 2 hours per day.
|
Measuring heart pulse rate using a wrest smart watch.
Other Names:
Changes in Accommodation measured by auto refractometer before and after mobile battle ground gaming.
|
|
Post COVID-19 users of battle ground games (Group 2)
Adults with a recent history of COVID-19 (average of 6 months after onset of the disease) that returned to their normal life style and are using mobile battle ground games.
|
Measuring heart pulse rate using a wrest smart watch.
Other Names:
Changes in Accommodation measured by auto refractometer before and after mobile battle ground gaming.
|
|
Normal subjects not playing mobile games (Groups 3)
Normal subjects that are not using any action mobile games.
|
Measuring heart pulse rate using a wrest smart watch.
Other Names:
Changes in Accommodation measured by auto refractometer before and after mobile battle ground gaming.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Changes in heart pulse rate
Time Frame: During playing mobile battle ground games
|
Changes in pulse in each group members measured by smart wrest watch in pulse beat/per minute.
|
During playing mobile battle ground games
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Changes in accommodation
Time Frame: Before and immediately after mobile battle ground games
|
Changes in eye accommodation measured by auto refractometer in diopter (D).
|
Before and immediately after mobile battle ground games
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Chair: Mohamed A Abdelshafy, MD, Benha University
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)
May 10, 2022
Primary Completion (Anticipated)
February 10, 2023
Study Completion (Anticipated)
February 20, 2023
Study Registration Dates
First Submitted
May 12, 2022
First Submitted That Met QC Criteria
May 12, 2022
First Posted (Actual)
May 17, 2022
Study Record Updates
Last Update Posted (Actual)
May 17, 2022
Last Update Submitted That Met QC Criteria
May 12, 2022
Last Verified
May 1, 2022
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- RC 10-22
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Undecided
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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