Comparing different methods for correcting myopia in youth
A Comparative Study on the Clinical Efficacy, Quality of Life, and Cost of Use of Peripheral Defocus Spectacles, Frame Glasses, and Orthokeratology Lenses in Myopic Children and Adolescents
He Eye Hospital · NCT06278974
This study tests which of three methods for correcting nearsightedness—special glasses, regular glasses, or contact lenses worn overnight—works best for kids aged 13 to 17 and how it affects their daily lives.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 90 (estimated) |
| Ages | 7 Years to 17 Years |
| Sex | All |
| Sponsor | He Eye Hospital (other) |
| Locations | 1 site (Shenyang, Liaoning) |
| Trial ID | NCT06278974 on ClinicalTrials.gov |
What this trial studies
This research evaluates the effectiveness, quality of life impact, and cost of three myopia correction methods in children aged 13-17 years: peripheral defocus spectacles, standard frame glasses, and orthokeratology lenses. The study involves a cohort of 300 myopic children with a refractive error between -1.00D and -6.00D, assessing their psychological, social, and educational experiences over one year. By comparing these methods, the study aims to provide valuable insights for parents and healthcare providers in choosing the most suitable correction options for young patients.
Who should consider this trial
Good fit: Ideal candidates are children aged 13-17 years with myopia between -1.00D and -6.00D who have not previously used any of the correction methods being studied.
Not a fit: Patients with other eye conditions, recent eye surgeries, or severe psychological disorders may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could help identify the most effective and cost-efficient myopia correction method, improving the quality of life for affected youth.
How similar studies have performed: While there have been studies on myopia correction methods, this specific comparative approach focusing on quality of life and cost-effectiveness is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Children aged 7-17 years. * Myopia between -1.00D and -6.00D; astigmatism \<±1.5D; best corrected visual acuity ≥1.0. * First-time spectacle wearers who use a single correction method and meet the indications for it (any one of orthokeratology lenses, single-vision frame glasses, or myopia control frame glasses) * Willing to participate in the entire research process and complete all the examinations, questionnaires and cost records as required. * Be able to maintain contact throughout the research period, such as having a fixed address and contact information. Exclusion Criteria: * History of strabismus, amblyopia, refractive disparity or retinal diseases * Previous history of eye surgery * Severe psychological disorders or behavioral problems * History of allergy to contact lenses or contact lens care solutions
Where this trial is running
Shenyang, Liaoning
- HeEyeHospital — Shenyang, Liaoning, China (RECRUITING)
Study contacts
- Principal investigator: ruyi Li — He Eye Hospital
- Study coordinator: lan Hu
- Email: hulan@hsyk.com.cn
- Phone: +8615940406919
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Myopia, Cost-effectiveness Analysis, Quality of Life, youth, glasses