N/A
N=53
Investigation of Wearing Compliance of Spectacles for Myopia Control
Myopia
Bottom Line
View on ClinicalTrials.gov: NCT06590441 ↗Enrolled (actual)
53
Serious AEs
0.0%
Results posted
Nov 2025
Primary outcome: Primary: Overall Wearing Pattern of Myopia Control Spectacles — 12.8 Hours in a day
Study Design & Population
- Study type
- Observational
- Phase
- N/A
- Interventions
- Myopia control spectacles (Device)
- Age
- Pediatric · 6+ yrs
- Sex
- All
- Sponsor
- CooperVision, Inc.
- Primary completion
- Jan 2025
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Overall Wearing Pattern of Myopia Control Spectacles |
12.8 | — |
| PRIMARY Effect of Sex on Overall Wearing Pattern |
12; 10.4; 13.9; 11.5 | — |
Summary
The goal of this observational study was to compare the wearing patterns of spectacles prescribed for myopia control in juvenile wearers.
Eligibility Criteria
Inclusion Criteria
- They are aged between six and 15 years old.
- Their parent or guardian understands the rights of the subject and are willing to sign a statement of informed consent.
- They understand the study at a level appropriate for their age and are willing to sign a statement of assent.
- They and their parents or guardians are willing and able to follow the protocol.
- They currently use spectacle lenses for myopia control and have done so for at least three months.
- They agree not to participate in other clinical research for the duration of this study.
Exclusion Criteria
- They have an unusual ophthalmic history, which in the opinion of the site investigator or Principal Investigator might impact on the successful conduct of the study.
- They are amblyopic.
Data sourced from ClinicalTrials.gov (NCT06590441). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.