Ocular and Cardiac Effects of Battle Ground

Sponsor
Benha University (Other)
Overall Status
Recruiting
CT.gov ID
NCT05377931
Collaborator
(none)
150
1
9.4
16

Study Details

Study Description

Brief Summary

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.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: Changes in heart pulse rate
  • Diagnostic Test: Changes in eye strain

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 Design

Study Type:
Observational
Anticipated Enrollment :
150 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Ocular and Cardiac Effects of Mobile Battle Ground Games
Actual Study Start Date :
May 10, 2022
Anticipated Primary Completion Date :
Feb 10, 2023
Anticipated Study Completion Date :
Feb 20, 2023

Arms and Interventions

Arm 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.

Diagnostic Test: Changes in heart pulse rate
Measuring heart pulse rate using a wrest smart watch.
Other Names:
  • Pulse oximeter changes
  • Diagnostic Test: Changes in eye strain
    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.

    Diagnostic Test: Changes in heart pulse rate
    Measuring heart pulse rate using a wrest smart watch.
    Other Names:
  • Pulse oximeter changes
  • Diagnostic Test: Changes in eye strain
    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.

    Diagnostic Test: Changes in heart pulse rate
    Measuring heart pulse rate using a wrest smart watch.
    Other Names:
  • Pulse oximeter changes
  • Diagnostic Test: Changes in eye strain
    Changes in Accommodation measured by auto refractometer before and after mobile battle ground gaming.

    Outcome Measures

    Primary Outcome Measures

    1. Changes in heart pulse rate [During playing mobile battle ground games]

      Changes in pulse in each group members measured by smart wrest watch in pulse beat/per minute.

    Secondary Outcome Measures

    1. Changes in accommodation [Before and immediately after mobile battle ground games]

      Changes in eye accommodation measured by auto refractometer in diopter (D).

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 40 Years
    Sexes Eligible for Study:
    All
    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.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Ahmed Abdelshafy Banhā QA Egypt 13511

    Sponsors and Collaborators

    • Benha University

    Investigators

    • Study Chair: Mohamed A Abdelshafy, MD, Benha University

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Ahmed Abdelshafy, Lecturer of Ophthalmology, Benha University
    ClinicalTrials.gov Identifier:
    NCT05377931
    Other Study ID Numbers:
    • RC 10-22
    First Posted:
    May 17, 2022
    Last Update Posted:
    May 17, 2022
    Last Verified:
    May 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    Undecided
    Plan to Share IPD:
    Undecided
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Ahmed Abdelshafy, Lecturer of Ophthalmology, Benha University
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of May 17, 2022