ATEG: Access to EyeGlasses for School-aged Children

Sponsor
Boston Children's Hospital (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05588362
Collaborator
Fitz Frames, Inc. (Other)
72
2
10.9

Study Details

Study Description

Brief Summary

Uncorrected refractive error is a leading cause of visual impairment in children and can impact vision, quality of life, and academic performance. Despite Boston Children's Hospital serving patients from a wide range of socioeconomic backgrounds, there are health disparities in access to eyeglasses as a consequence of patients' health insurance. The investigators will examine whether the use of an in-clinic app for 3-D printed glasses reduces disparities in access to eyeglasses for our patients on Medicaid. The intervention will address social determinants of health and improve pediatric health outcomes namely, how and when children having publicly funded health insurance receive eyeglasses. The short-term objectives are (1) to compare the time to receive glasses between publicly funded MassHealth eyeglasses and an in-clinic order of 3D printed glasses (2) to evaluate compliance with glasses wear in these two groups, and (3) to evaluate visual function and quality-of-life outcomes in these two groups. This prospective randomized control study will evaluate barriers to accessing eyeglasses in school-aged children. The investigators will recruit children enrolled in MassHealth and randomize them into two cohorts: (1) the control group will receive MassHealth glasses as per standard of care, through an optical shop of their choosing, or (2) the intervention group will use an app for immediately ordering glasses (paid for by the study) in clinic following their appointment. The investigators will evaluate the time needed to receive eyeglasses, compliance with glasses wear, quality of life, and visual outcomes between the cohorts at one-, three-, and six-month intervals. Through this project, the investigators will not only evaluate, quantify, and bring awareness to disparities in our patient population, but will also look toward finding a solution through the use of a novel application that addresses many of the barriers faced by patients insured through Medicaid.

Condition or Disease Intervention/Treatment Phase
  • Other: Fitz Frames 3-D Printed Glasses
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
72 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Prospective randomized control studyProspective randomized control study
Masking:
Double (Investigator, Outcomes Assessor)
Masking Description:
Investigators responsible for administering questionnaires and collecting visual outcomes will be masked to the treatment group of the participant. Both the research assistant and participant will be unmasked.
Primary Purpose:
Treatment
Official Title:
Access to EyeGlasses for School-aged Children
Anticipated Study Start Date :
Feb 1, 2023
Anticipated Primary Completion Date :
Nov 30, 2023
Anticipated Study Completion Date :
Dec 30, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Fitz Frames 3-D Printed Glasses

The intervention group will order glasses directly in the office following their exam and consent using an iPad with the help of the research assistant. The iPad will be e-connected to a 3D printed glasses manufacturer (Fitz Frames) through their application, allowing the child (with assistance from the doctor or research assistant) to take various measurements in real time. Sixteen different measurements will be taken including interpupillary distance, face length, face width, and temple measures. The child will be able to choose frame style and order it directly from the manufacturer immediately following the exam. Glasses will be shipped directly to the patient's home (shipping address will be input to the app by the family).

Other: Fitz Frames 3-D Printed Glasses
The intervention group will order glasses directly in the office following their exam and consent using an iPad with the help of the research assistant. The iPad will be e-connected to a 3D printed glasses manufacturer (Fitz Frames) through their application, allowing the child (with assistance from the doctor or research assistant) to take various measurements in real time. Sixteen different measurements will be taken including interpupillary distance, face length, face width, and temple measures. The child will be able to choose frame style and order it directly from the manufacturer immediately following the exam. Glasses will be shipped directly to the patient's home (shipping address will be input to the app by the family).

No Intervention: Traditional Glasses Procurement Group

(1) The control group will receive standard of care in which a prescription for glasses will be dispensed as a paper copy prescribed by the examiner before randomization. The research assistant will use a script (attached) that instructs families how to procure glasses traditionally through Masshealth. The participant/family will be instructed to bring the paper prescription to an optical shop that carries MassHealth frames. A printout of local optical shops that carry MassHealth frames will be provided to the patient.

Outcome Measures

Primary Outcome Measures

  1. Compliance [Six months]

    Glasses compliance will be assessed with self-reported calendar

  2. Quality of Life Questionnaire [Baseline, will be collected at enrollment visit]

    Quality of life measures using the PedEyeQ

  3. Distance visual acuity [Baseline, will be collected at enrollment visit]

    Linear Snellen optotypes (age >6) or HOTV matching with crowding bars (age <6)

  4. Distance visual acuity [0-3 Months, will be collected at 3 month visit]

    Linear Snellen optotypes (age >6) or HOTV matching with crowding bars (age <6)

  5. Distance visual acuity [3-6 Months, will be collected at 6 month visit]

    Linear Snellen optotypes (age >6) or HOTV matching with crowding bars (age <6)

  6. Stereoacuity [Baseline, will be collected at enrollment visit]

    Stereo Fly test

  7. Stereoacuity [0-3 Months, will be collected at 3 month visit]

    Stereo Fly test

  8. Stereoacuity [3-6 Months, will be collected at 6 month visit]

    Stereo Fly test

  9. Ocular alignment [Baseline, will be collected at enrollment visit]

    Alternative prism cover test at distance and at near

  10. Ocular alignment [0-3 Months, will be collected at 3 month visit]

    Alternative prism cover test at distance and at near

  11. Ocular alignment [3-6 Months, will be collected at 6 month visit]

    Alternative prism cover test at distance and at near

  12. Near point of convergence [Baseline, will be collected at enrollment visit]

    Near point of convergence (break point and recovery) will be measured using an accommodative target

  13. Near point of convergence [0-3 Months, will be collected at 3 month visit]

    Near point of convergence (break point and recovery) will be measured using an accommodative target

  14. Near point of convergence [3-6 Months, will be collected at 6 month visit]

    Near point of convergence (break point and recovery) will be measured using an accommodative target

  15. Near visual acuity [Baseline, will be collected at enrollment visit]

    Near visual acuity will be measured at 40 cm using the Rosenbaum card

  16. Near visual acuity [0-3 Months, will be collected at 3 month visit]

    Near visual acuity will be measured at 40 cm using the Rosenbaum card

  17. Near visual acuity [3-6 Months, will be collected at 6 month visit]

    Near visual acuity will be measured at 40 cm using the Rosenbaum card

  18. Quality of Life Questionnaire- PedEyeQ [0-3 Months, will be collected at 3 month visit]

    Quality of life measures using the PedEyeQ

  19. Quality of Life Questionnaire- PedEyeQ [3-6 Months, will be collected at 6 month visit]

    Quality of life measures using the PedEyeQ

Eligibility Criteria

Criteria

Ages Eligible for Study:
5 Years to 17 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Masshealth insurance

  • first-time glasses wearers

  • receive a diagnosis of refractive amblyopia, myopia, hyperopia and/or astigmatism requiring spectacle correction for optimal vision at distance and near.

  • Glasses must be recommended for full time wear by the attending optometrist or ophthalmologist

Exclusion Criteria:
  • strabismus

  • developmental or learning delay

  • other ocular pathology

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Boston Children's Hospital
  • Fitz Frames, Inc.

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Emily Wiecek, Optometrist, Boston Children's Hospital
ClinicalTrials.gov Identifier:
NCT05588362
Other Study ID Numbers:
  • IRB-P00040587
First Posted:
Oct 20, 2022
Last Update Posted:
Jan 11, 2023
Last Verified:
Jan 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jan 11, 2023