ClinicalTrials.gg
RecruitingNCT07490444Updated Jul 20, 2026

Metric-Optimized Spectacle Prescriptions for Children With Down Syndrome

A Phase 2 interventional study of Metric-optimized spectacles and Routine Clinical Spectacles in Refractive Error Correction and Visual Acuity, sponsored by Ohio State University. Recruiting at 1 site in United States. Open to participants aged 5 Years to 12 Years. Per ClinicalTrials.gov, last updated 2026-07-20.

Sponsored by Ohio State University · Phase 2, Interventional, and Treatment

From the registry’s dates

  • Started Jul 2026; still recruiting 3 months later.
Phase
Phase 2
Study type
Interventional
Enrollment
24
Allocation
Randomized
Ages
5 Years to 12 Years
Sex
All
01

Study summary

This study seeks to determine whether glasses prescriptions determined from computer analysis of detailed images of the eyes provide better vision outcomes for children with Down syndrome than prescriptions determined using routine clinical methods.

Read the detailed description

The purpose of this study is to test the hypothesis that metric-derived spectacle prescriptions based on wavefront aberration measurements of the eyes of children with Down syndrome can provide an improvement in visual acuity over that obtained with spectacle prescriptions based on standard clinical prescribing techniques. Twenty-four children with Down syndrome will be enrolled to participate in this phase II clinical trial of spectacle prescriptions. The study is a randomized, cross-over design with two treatment arms that will consist of 5 study visits over the course of 12 months for each participant.

Participant eligibility will first be assessed at an enrollment exam by an unmasked examiner. Individuals enrolled in the study will have distance refraction measured with an open-field autorefractor (Grand Seiko), pupil size measured with an infrared camera in both normal and dim room illumination, and wavefront aberration measured with the Complete Ophthalmic Analysis System (COAS) wavefront aberrometer. Following the enrollment exam, the metric-optimized refraction (treatment arm 1) will be determined from the wavefront measurements. A clinical examiner (who will later serve as a masked examiner) will perform a complete eye examination on the participants at the enrollment exam to include presenting distance and near visual acuity, measures of binocular function (depth perception, eye alignment), and collection of data from any clinical techniques indicated to determine what she believes to be the best clinical refraction for each individual participant. This may include the prescription of a bifocal, given evidence that the majority of individuals with Down syndrome do not have adequate accommodation and may benefit from bifocal prescriptions. Participants will then select a single frame for their new spectacle prescriptions from the College of Optometry's Eyewear Gallery. Two identical frames will be ordered to produce the spectacles for the two treatment arms. If a bifocal was prescribed by the clinical examiner, the same bifocal power will be included for both refractions to maintain an equal shift in the image plane for near viewing with each prescription. Throughout the examination, the parent/guardian of each participant will complete the Vineland Behavioral Assessment survey about the participant's adaptive abilities. This survey will be scored by study personnel to assign an adapted age to the patient as an indication of their developmental ability. Data will later be analyzed with this adapted age as a predictor variable to identify associations between acuity and developmental ability.

Participants will return for a dispensing visit when the spectacles are ready. At the initial dispensing visit, an unmasked examiner will verify the power of each pair of spectacles and label them according to the randomization order for dispensing. A masked examiner will then perform both distance and near visual acuity, as well as binocularity testing (cover test and near stereoacuity) for the participant's presenting correction (unaided if they do not currently wear spectacles) and each of the experimental prescriptions. The values for the experimental prescriptions will be compared to the presenting measures to ensure participants are not dispensed spectacles that provide worse visual function than they had when presenting to the study. Any experimental prescription which causes visual acuity to degrade more than 3 lines from presenting acuity at either distance or near, depth perception to decrease more than 2 levels from presenting, or results in the manifestation of an eye-turn that was previously not observed, will not be dispensed to the patient provided findings are confirmed on a re-test the day the prescription is randomized for dispense. Prescriptions passing this safety check will be dispensed to the participant one at a time in random order for two month wearing intervals with a Smart Button data logger placed in a mount on the temple of the spectacles. The data logger will provide an objective assessment of spectacle wear time for each prescription. The decision to select a two month wear interval was based on clinical experience related to patient adaptation time to new spectacle corrections, scientific evidence for perceptual adaptation time to previously uncorrected astigmatic refractive error, the time course expected for the most rapid improvement in vision in children previously uncorrected, and a desire to allow adequate time for assessment of the wearing profile of each individual. Participants will be asked to return at two-month intervals to perform adapted visual acuity measures, download data logger readings, and complete a brief survey regarding their opinion of each spectacle treatment.

After completion of both spectacle prescription dispensing periods, the clinical examiner will determine, through evaluation of all clinical measures and consultation with the patient and their parent/guardian, which pair of spectacles is recommended for continued wear. This decision will occur without un-masking the examiner or the participant. Participants will be asked to return for one additional follow-up after 6 months additional wear of the recommended prescription. At the follow-up visit, visual acuity and binocularity will be measured to determine whether additional improvements occur with continued spectacle wear.

The primary outcome measure for this study is comparison of 2 month adapted visual acuity between prescriptions. The small within subject variability in visual acuity translates into high study power for comparisons in the cross-over study. For our sample size, we have greater than 99% power to detect a difference of 7 letters. However, given that the desired statistical analysis includes not only adapted visual acuity, but also compliance, via temperature sensors, and survey scores, a sample size of 24 provides greater than 80% power to detect effect size values of 0.80 (large effect) or higher for these factors.

02

Conditions studied

  • Refractive Error Correction
  • Visual Acuity

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Keywords

  • Down syndrome
  • Children
  • Glasses
  • Spectacles
  • Vision
03

In context

Down Syndrome

438 studies on the registry are indexed under Down Syndrome; 99 are open to participants now.

This study's planned enrollment of 24 is below the median of 37 across 286 interventional studies indexed under Down Syndrome.

Browse Down Syndrome studies →

Lead sponsor

Ohio State University is the lead sponsor of 663 studies on the registry; 148 are open to participants now.

Of its 67 completed or terminated interventional studies of FDA-regulated products, 49 (73%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
5 Years to 12 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Down syndrome
  • Age 5 to 12 years
  • Ability to sit for study measures
  • Able to be dilated

Exclusion criteria

Exclusion Criteria:

  • Nystagmus
  • History of Ocular or Refractive Surgery
  • Corneal or lenticular opacities
  • Ocular disease
  • Anisometropic or strabismic amblyopia
  • Contact allergy to aluminum
05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Crossover assignment
Masking
Triple (Participant, Care provider, Outcomes assessor)
Enrollment
24 participants (estimated)

Study arms

  • Experimental
    Metric-Optimized First, Clinical Second

    Participants will be dispensed the metric-optimized spectacle correction for the first two months followed by the clinically determined spectacle correction for the second two months.

    Device: Metric-optimized spectacles · Device: Routine Clinical Spectacles

  • Experimental
    Clinical First, Metric-Optimized Second

    Participants will be dispensed the clinical spectacle refraction for the first two months followed by the metric-optimized correction for the second two months.

    Device: Metric-optimized spectacles · Device: Routine Clinical Spectacles

Interventions

  • DeviceMetric-optimized spectacles

    Metric-optimized spectacles are glasses made from a prescription determined by the optimization of a metric for retinal image quality, Visual Strehl Ratio (VSX), as determined by algorithms utilizing wavefront aberration measures of the eye

  • DeviceRoutine Clinical Spectacles

    Routine clinical spectacles are glasses made from a prescription based upon findings that are obtained during a routine eye examination, including autorefraction measures.

06

What researchers measure

Primary outcomes

  1. Adapted Distance Visual Acuity

    Aided LogMAR (minimum angle of resolution) distance visual acuity obtained with either British Standard Letters or HOTV - matching for participants unable to name letters

    Time frame: 2 months

Secondary outcomes

  1. Initial Distance Visual Acuity

    Aided LogMAR (minimal angle of resolution) distance visual acuity obtained with either British Standard Letters or HOTV - matching for participants unable to name letters

    Time frame: 1 day

  2. Near Visual Acuity

    Near LogMAR (minimum angle of resolution) visual acuity will be measured with a Bailey-Lovie style HOTV card

    Time frame: 2 months

  3. Spectacle Wear Time

    Total wear time of each pair of spectacles as measured objectively by a temperature sensor data logger mounted to the spectacle temple

    Time frame: 2 months

  4. Participant Survey

    Four question custom written survey with each question rated on a 5 point frown to smile scale. Questions target whether the subject likes the spectacles, feels they have good vision at distance and near, and feels that they see better with the spectacles than without. The lowest score is 1 and the highest score is 5 with 5 indicating better vision and higher preference for spectacles.

    Time frame: 2 months

07

Study locations

1 of 1 sites recruiting
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Jul 2026 (actual). Primary completion is estimated for Dec 2027, 16 months after the start.

Of 21 phase 2 interventional studies under Down Syndrome, half reached primary completion within 36 months of starting (the median), counting those still running; a quarter within 26 and three quarters within 61. This study's planned 16 months is below that.

How these figures are worked out, and which studies are left out of them.

Registered
Mar 18, 2026
First posted
Mar 24, 2026
StartActual
Jul 13, 2026
Primary completionEst.
Dec 1, 2027
CompletionEst.
May 1, 2028
Last update
Jul 20, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Jul 20, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07490444
Responsible party
Heather Anderson OD, PhD (Professor, Ohio State University) — Principal investigator
First posted
Mar 24, 2026
Start date
Jul 13, 2026
Primary completion
Dec 1, 2027 (estimated)
Completion
May 1, 2028 (estimated)
Last update
Jul 20, 2026

Study contacts

Heather Anderson, OD, PhD
Contact
anderson.3881@osu.edu
614-247-5825

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
Yes
View the source record on ClinicalTrials.gov ↗

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