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Recruiting NCT07571538

NCT07571538 VisionApp - Ghosting

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Clinical Trial Summary
NCT ID NCT07571538
Status Recruiting
Phase
Sponsor Indiana University
Condition Diplopia, Monocular
Study Type INTERVENTIONAL
Enrollment 12 participants
Start Date 2025-10-10
Primary Completion 2026-08-01

Eligibility & Interventions

Sex All sexes
Min Age 8 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
Proclear 1 Day Contact LensMyDay Contact LensNaturalVue Contact Lens

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 12 participants in total. It began in 2025-10-10 with a primary completion date of 2026-08-01.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

Recent Android mobile device technology is available which allows user-measured refractive error and reading add power. This technology could be quite useful to the clinical and research community. The current study aims to evaluate the accuracy, repeatability, and reproducibility of one such technology by VisionApp, specifically with regard to ghosting vision. VisionApp is an app which runs on a smartphone or other device which uses the distance between the user's face and the phone to determine refractive error, while the user looks at different targets (lines, letters, words, etc).

Eligibility Criteria

Inclusion Criteria: * has a refractive error between Plano and -5.00 D of sphere and cylinder components combined. * has refractive cylinder (e.g., astigmatism) of -0.75 D or less * has had a self-reported oculo-visual exam in the last 2 years * has best-corrected visual acuity of at least 20/20 in each eye * is not amblyopic or does not have any diagnosed ocular disease * is willing and able to follow instructions and maintain the appointment schedule Exclusion Criteria: * has any systemic disease affecting ocular health and visual acuity * is currently using any systemic or topical medications that could affect ocular health and visual acuity * is participating in another eye related research study

Contact & Investigator

Central Contact

Pete Kollbaum, PhD

✉ kollbaum@iu.edu

📞 812-555-5500

Frequently Asked Questions

Who can join the NCT07571538 clinical trial?

This trial is open to participants of all sexes, aged 8 Years or older, studying Diplopia, Monocular. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07571538 currently recruiting?

Yes, NCT07571538 is actively recruiting participants. Contact the research team at kollbaum@iu.edu for enrollment information.

Where is the NCT07571538 trial being conducted?

This trial is being conducted at Bloomington, United States.

Who is sponsoring the NCT07571538 clinical trial?

NCT07571538 is sponsored by Indiana University. The trial plans to enroll 12 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology