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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04068129
Other study ID # ABCD GCK Kaleidos
Secondary ID
Status Completed
Phase
First received
Last updated
Start date February 11, 2019
Est. completion date April 15, 2019

Study information

Verified date August 2019
Source Alaska Blind Child Discovery
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

"Adaptica" (Padova, Italy) designed a fixed-distance, dark portable tube with power and remote control for the "2WIN: photoscreener. GoChecksKids designed a flash-concentrating case for the iPhone 7+ to more quickly achieve two-axis photoscreen. These devices were compared to confirmatory exams in children and young adults in a remote Burma clinic and in an Alaskan pediatric ophthalmology practice.


Description:

Photoscreening with follow up confirmatory exams for referred and passed interpretations were offered to children and young adults at a remote clinic in the Karen State of eastern Burma (Myanmar). The clinic had intermittent 220 Volt power generator, but no internet or cell phone coverage. Consecutive patients in a "WiFi-equipped" pediatric ophthalmology practice in Anchorage, Alaska had photoscreening before confirmatory examination. Each patient had photoscreening with the "2WIN" photoscreener installed in the "Kaleidos" housing. In Anchorage, the devise was controled by the wireless tablet computer. In Burma, however, despite a "WiFi router" not connected to internet, the tablet computer would not connect to the 2WIN and therefore the "Kaleidos" read-trap door was opened so the 2WIN could be activated and controlled manually. The" 2WIN" stored results on an "micro-SD" memory card which was eventually downloaded to computer. Each patient also had photoscreening with GoCheckKids (GCK) on an "iPhone 7 Plus" using the enhanced, flash-concentrating cell-phone case. In Anchorage, in addition to on-site smart-phone interpretation, images were uploaded to the central reading center for secondary interpretation. In Burma, all images were retained on the smart phone and eventually uploaded for GoCheckKids central secondary analysis after return to urban internet availability. In Burma, a portable, light-wieght tent was used to provide a dim screening environment with less distraction. Confirmatory exams were performed consistent with 2003 and 2013 American Association for Pediatric Ophthalmology and Strabismus (AAPOS) uniform guidelines. Cycloplegic refractions were performed 20-40 minutes after cyclopentolate 1% instillation. Visual acuity was checked with patched, surround "HOTV" at 3 meters threshold with at least 3 of 4 optotypes correct. Validation was performed with conventional 2 x 2 screen-exam matrix, and also with Alaska Blind Child Discovery (ABCD) 3 x 3 matrix including inconclusive results (no instrument interpretation or unable to gain a reading) with inconclusive interpretations considered a referral.


Recruitment information / eligibility

Status Completed
Enrollment 162
Est. completion date April 15, 2019
Est. primary completion date April 12, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 6 Months to 40 Years
Eligibility Inclusion Criteria: - at least one eye Exclusion Criteria: - bilateral enucleation

Study Design


Related Conditions & MeSH terms


Intervention

Device:
photoscreen
Determine amblyopia risk factors

Locations

Country Name City State
United States Alaska Children's EYE & Strabismus Anchorage Alaska

Sponsors (1)

Lead Sponsor Collaborator
Alaska Blind Child Discovery

Country where clinical trial is conducted

United States, 

References & Publications (1)

Martin SJ, Htoo HE, Hser N, Arnold RW. Performance of Two Photoscreeners Enhanced by Protective Cases. Clin Ophthalmol. 2020 May 25;14:1427-1435. doi: 10.2147/OPTH.S251451. eCollection 2020. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Amblyopia Rick Factor prevalence AAPOS 2003 and 2013 defined ARFs February 15, 2019 through April 16, 2019
Secondary Refractive Error Glasses prescription February 15, 2019 through April 16, 2019
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