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Multicenter Evaluation of Near Vision and Outdoor Time in Kids Study

NCT06119243 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 230

Last updated 2024-12-12

No results posted yet for this study

Summary

Currently, optical and pharmacological interventions have been developed to prevent the progression of childhood myopia. However, no myopia control strategy has been shown to have complete efficacy in controlling myopia progression in children. One possible reason is that risk factors contributing to the development of myopia were not controlled in previous clinical studies including time outdoors and near vision behaviour. This study aims to quantify time spent outdoors and near vision behavior in myopic children and its impact on myopia control efficacy. The outcomes of this study will guide clinicians on risk management and improve responses to existing treatments for progressive myopia.

Conditions

  • Myopia

Interventions

DEVICE

Vivior

The Vivior is a wearable clip-on sensor that objectively quantifies near viewing distance and duration, and ambient illumination. The Vivior will be attached to the spectacles frame of children undergoing myopia control treatment.

Sponsors & Collaborators

  • Queensland University of Technology

    collaborator OTHER

  • New England College of Optometry

    collaborator OTHER

  • State University of New York College of Optometry

    collaborator OTHER

  • University of California, Berkeley

    collaborator OTHER

  • The University of New South Wales

    lead OTHER

Eligibility

Min Age
4 Years
Max Age
14 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-03-21
Primary Completion
2026-06-30
Completion
2026-12-31

Countries

  • United States
  • Australia

Study Locations

More Related Trials

Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06119243 on ClinicalTrials.gov