Mobile Medical Application for Cost-effective Strabismus Screening
Primary Purpose
Strabismus
Status
Unknown status
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
EyeTurn App
Sponsored by
About this trial
This is an interventional screening trial for Strabismus focused on measuring Double Vision, Amblyopia
Eligibility Criteria
Inclusion Criteria:
Ground Truth Aim Study (closed for recruitment):
- Age 18 to 88
- Normal or corrected to normal vision
Clinical Aim Study:
- Ages 18 to 88
- Strabismus
- Able to keep looking at a visual target for 30-60 seconds
- Able to report locations of visual targets during testing
Exclusion Criteria:
Ground Truth Aim Study:
- Age less than 18 or greater than 88.
Clinical Study:
- Age less than 18 or greater than 88
- Inability to keep looking at a visual target for 30-60 seconds
- Inability to report locations of visual targets during testing
Sites / Locations
- Ophthalmology of Clinical Research Office, Mass Eye and EarRecruiting
Arms of the Study
Arm 1
Arm Type
Other
Arm Label
EyeTurn App
Arm Description
All participants will have their eye alignment measured with both the experimental device (EyeTurn app) and the clinical gold standard tests or ground truth (simulated strabismus gaze angles).
Outcomes
Primary Outcome Measures
Strabismus angle with the app compared to ground truth and gold standard tests
Strabismus angle is typically reported in prism diopters (PD) where 1PD = 0.57degrees.
Secondary Outcome Measures
Perceived Value Survey
A 10 point likert-type rating scale to quantify the perceived value (1 low value to 10 high value) of the app tele-strabismus consultation (a subaim in the clinical evaluation aim)
Test-Retest repeatability of the app
Strabismus angle
Robustness
calculation of the percentage of capture failures (capture failures/ total number of attempted image captures)
Full Information
NCT ID
NCT03450980
First Posted
February 7, 2018
Last Updated
April 16, 2021
Sponsor
Massachusetts Eye and Ear Infirmary
Collaborators
National Eye Institute (NEI)
1. Study Identification
Unique Protocol Identification Number
NCT03450980
Brief Title
Mobile Medical Application for Cost-effective Strabismus Screening
Official Title
Mobile Medical Application for Cost-effective Strabismus Screening
Study Type
Interventional
2. Study Status
Record Verification Date
April 2021
Overall Recruitment Status
Unknown status
Study Start Date
February 1, 2018 (Actual)
Primary Completion Date
December 30, 2019 (Actual)
Study Completion Date
December 30, 2022 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Massachusetts Eye and Ear Infirmary
Collaborators
National Eye Institute (NEI)
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Develop and evaluate a new smartphone based app to screen for and measure eye misalignment (strabismus). The investigators will validate the app against simulated strabismus of known magnitude and common clinical tests. They will evaluate the app as a screening tool in high risk populations, to determine the sensitivity and specificity. They hypothesize that the app can measure to within 2 units (prism diopters) of the ground truth, and that it will be correlated with gold standard tests.
Detailed Description
The goal of the proposed project is the development and evaluation of a novel mobile medical application for the detection and monitoring of strabismus (eye misalignment). The image analysis technology necessary to measure strabismus using the corneal reflection technique (Photographic Hirschberg Test) has been available for many decades, however it has never been deployed using a smart phone. A smart phone platform will eliminate barriers of cost (since the hardware is maintained and updated by the smart phone industry), leading to rapid wide spread application and allowing the technology to finally reach its potential level of impact for children's eye care in the detection and management of strabismus. Strabismus causes visual confusion and double vision which ultimately results in the brain suppressing vision from the deviated eye. In children this results in under-development (amblyopia) with permanent vision loss in the deviated eye if not detected and treated at a young age. Strabismus in children is also associated with coordination problems such as postural instability and severe social disadvantages. Strabismus develops in an estimated 3-8% of children in the U.S. The prototype smart phone app (Referred to here as the Mobile Eye Alignment App - MEAA), uses photographic analysis of the corneal reflection (Purkinjie image) generated by the smart phone camera flash. The corneal reflection method uses the displacement of the reflection from the center of the pupil in the deviated eye to calculate the amount of eye misalignment. This measurement technique will be deployed for the proposed project using the hardware of the iPhone, a popular phone with an iOS operating system. Preliminary results suggest the app can measure differences in eye alignment of 1.6° (2.8 prism diopters). If successfully developed, the app has potential to be utilized to advance pediatric strabismus research by facilitating and reducing the cost of collecting enormous amounts of data from the general population and under-served or remote populations for epidemiological studies, and allowing researchers to capture eye alignment data much more frequently than is currently possible. Such a tool could better delineate the natural history of strabismus and perhaps help determine its causes. While devices are available which could make these measurements, the costs are prohibitively high (>$3,000 ea.) and will not reach the widespread availability of smart phones. Clinical goals for the app are to provide eye doctors with an objective measurement tool in the exam room, allow daily monitoring of treatment effects, and eventually to be used as a screening tool by school nurses, pediatricians, and parents. The barriers to market success of stand-alone devices is not the accuracy sensitivity or specificity of photographic analysis technique which has been reported with sensitivity from 53% to near 90% and specificity ranging from 76% to 94% for strabismus detection. Impact of strabismus screening for the young - Early detection for strabismus in young children, especially during the critical period up to 2 years of age, is important to ensure that treatment is administered as soon as possible. The success of amblyopia treatment depends on several factors, but principally on the age of onset and the age at which the treatment is initiated. Therapy for amblyopia is maximally effective if started before age 3 and can be initiated as early as 8 months, underscoring the critical need for early and widespread access to strabismus screening. Indeed, countries with long-standing early vision screening programs have reported significantly reduced rates of amblyopia. Access to strabismus screening is also important for older, school age children (age 7-17) suffering from amblyopia, for whom treatment can lead to significant improvements in visual acuity ranging from 20%-70% of patients, depending on their age bracket.
Aims Specific Aim 1: Develop and test key functionality of the strabismus app by comparing measurements with successive versions of the prototype app to known angles of eye deviation (non-strabismic volunteers will gaze at off axis targets of known eccentricity). Specific Aim 2: Evaluate the strabismus app accuracy and feasibility in a clinical environment.
Primary Hypothesis: For strabismus ranging from 1 to 30 prism diopters (target range), the optimized version of the app will provide measurements which are not significantly different from the ground truth (simulated strabismus) or clinical tests of eye alignment.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Strabismus
Keywords
Double Vision, Amblyopia
7. Study Design
Primary Purpose
Screening
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Masking Description
Aim 1) In the comparison of the app against the ground truth the study staff will be masked to the ground truth value.
Aim 2) In comparison of the app against the clinical gold standards, the study staff making the clinical gold standard measures (prism alternating cover test and Modified Thorington test) will be masked to the app measurement.
Analyses: Study staff and statistician performing the analysis will be masked to which group data is from the app and which is from the ground truth and gold standard tests.
Allocation
N/A
Enrollment
190 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
EyeTurn App
Arm Type
Other
Arm Description
All participants will have their eye alignment measured with both the experimental device (EyeTurn app) and the clinical gold standard tests or ground truth (simulated strabismus gaze angles).
Intervention Type
Other
Intervention Name(s)
EyeTurn App
Intervention Description
App software which analyzes the position of ocular surface reflections in a photograph to quantify eye misalignment (strabismus)
Primary Outcome Measure Information:
Title
Strabismus angle with the app compared to ground truth and gold standard tests
Description
Strabismus angle is typically reported in prism diopters (PD) where 1PD = 0.57degrees.
Time Frame
15 minutes
Secondary Outcome Measure Information:
Title
Perceived Value Survey
Description
A 10 point likert-type rating scale to quantify the perceived value (1 low value to 10 high value) of the app tele-strabismus consultation (a subaim in the clinical evaluation aim)
Time Frame
5 minutes after completion of the tele-strabismus consult
Title
Test-Retest repeatability of the app
Description
Strabismus angle
Time Frame
3 app measurements taken over approximately 1 minute
Title
Robustness
Description
calculation of the percentage of capture failures (capture failures/ total number of attempted image captures)
Time Frame
1 year
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
88 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Ground Truth Aim Study (closed for recruitment):
Age 18 to 88
Normal or corrected to normal vision
Clinical Aim Study:
Ages 18 to 88
Strabismus
Able to keep looking at a visual target for 30-60 seconds
Able to report locations of visual targets during testing
Exclusion Criteria:
Ground Truth Aim Study:
Age less than 18 or greater than 88.
Clinical Study:
Age less than 18 or greater than 88
Inability to keep looking at a visual target for 30-60 seconds
Inability to report locations of visual targets during testing
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Sheryl Erwin, BS
Phone
617-912-2505
Email
sheryl_erwin@meei.harvard.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kevin E Houston, OD
Organizational Affiliation
Massachusetts Eye and Ear
Official's Role
Principal Investigator
Facility Information:
Facility Name
Ophthalmology of Clinical Research Office, Mass Eye and Ear
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
021141
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jan Trott, BS
Phone
617-573-6060
Email
ophthalmologyclinicalresearch@meei.harvard.edu
First Name & Middle Initial & Last Name & Degree
Kevin Houston
Phone
617-912-2525
Email
kevin_houston@meei.harvard.edu
First Name & Middle Initial & Last Name & Degree
Kevin E Houston, O.D., M.Sc.
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
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Citation
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Results Reference
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21833955
Citation
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Results Reference
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18962921
Citation
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Citation
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21489386
Citation
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Citation
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Citation
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Citation
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Citation
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Citation
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Citation
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Results Reference
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Mobile Medical Application for Cost-effective Strabismus Screening
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