VisionApp - Ghosting
21 sierpnia 2026 zaktualizowane przez: Pete Kollbaum, OD, PhD, Indiana University
Assessment of the Accuracy and Repeatability of the VisionApp - Ghosting Measurement Protocol
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).
Przegląd badań
Status
Status
Rekrutacyjny
Warunki
Warunki
Interwencja / Leczenie
Interwencja / Leczenie
Szczegółowy opis
Subjects will be enrolled at the Clinical Optics Research Lab at Indiana University.
At the study visit, demographic and health/ocular history may be collected by oral history and standard clinical testing including refraction (check of glasses prescription), auto-refraction or abbrerometry may be performed. Visual acuity and room lighting checks may also be measured using standard clinical techniques.
For the experimental portion of the study visit, participants will be asked to look at letters and describe any shadows or distortions they see using slider bars or numerical rating scales, while wearing different contact lenses. Participants will first be asked to wear commercially available single vision contact lenses to establish best corrected vision. A single vision lens will then remain in one eye, and participants will proceed with ghosting assessments using two different multifocal contact lenses worn in the other eye. Adult participants will perform the ghosting assessments while wearing 2 commercially available multifocal lenses, and children participants will perform the ghosting assessments while wearing a commercially available and investigational lens. Randomization will determine which lens is worn first.
If participants are unable to complete all testing in a single session, they may be permitted to return on a subsequent day.
Typ studiów
Typ studiów
Interwencyjne
Zapisy (Szacowany)
Zapisy
12
Faza
Faza
- Nie dotyczy
Kontakty i lokalizacje
Ta sekcja zawiera dane kontaktowe osób prowadzących badanie oraz informacje o tym, gdzie badanie jest przeprowadzane.
Kontakt w sprawie studiów
Kontakt w sprawie studiów
- Nazwa: Pete Kollbaum, PhD
- Numer telefonu: 812-555-5500
- E-mail: kollbaum@iu.edu
Lokalizacje studiów
-
-
Indiana
-
Bloomington, Indiana, Stany Zjednoczone, 47405
- Rekrutacyjny
- Clinical Optics Research Lab
-
Kontakt:
- Pete Kollbaum, PhD
- E-mail: kollbaum@iu.edu
-
-
Kryteria uczestnictwa
Badacze szukają osób, które pasują do określonego opisu, zwanego kryteriami kwalifikacyjnymi. Niektóre przykłady tych kryteriów to ogólny stan zdrowia danej osoby lub wcześniejsze leczenie.
Kryteria kwalifikacji
Kryteria kwalifikacji
Wiek uprawniający do nauki
- Dziecko
- Dorosły
- Starszy dorosły
Akceptuje zdrowych ochotników
Tak
Opis
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
Plan studiów
Ta sekcja zawiera szczegółowe informacje na temat planu badania, w tym sposób zaprojektowania badania i jego pomiary.
Jak projektuje się badanie?
Szczegóły projektu
- Główny cel: Diagnostyczny
- Przydział: Randomizowane
- Model interwencyjny: Zadanie krzyżowe
- Maskowanie: Brak (otwarta etykieta)
Liczba ramion
4
Broń i interwencje
Grupa uczestników / ArmGrupa uczestników / Arm |
Interwencja / LeczenieInterwencja / Leczenie |
|---|---|
|
Aktywny komparator: Adults: Lens 1, then Lens 2
Subjects will be asked to look at letters and describe any shadows or distortions they see using slider bars or numerical rating scales.
This will be performed twice, while wearing two different soft multifocal contact lenses in one eye.
The order in which the participant wears each of the multifocal contact lenses for these tasks will be randomized.
After the assessment while wearing the first multifocal lens is completed, subjects will repeat the task while wearing the second multifocal lens.
|
Proclear 1 day is a commercially available single vision soft contact lens for single use (daily wear).
Participants will wear these contacts at the beginning of the study visit to establish best corrected vision.
Participants will then continue to wear this contact lens in one eye for the duration of the study visit.
MyDay is a commercially available multifocal soft contact lens for daily wear.
Adult participants will assess images for ghosting while wearing a MyDay contact lens in one eye.
Order of exposure to this lens will be determined via randomization.
NaturalVue is a commercially available multifocal soft contact lens for daily wear.
Adult participants will assess images for ghosting while wearing a NaturalVue contact lens in one eye.
Order of exposure to this lens will be determined via randomization.
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.)
|
|
Aktywny komparator: Adults: Lens 2, then Lens 1
Subjects will be asked to look at letters and describe any shadows or distortions they see using slider bars or numerical rating scales.
This will be performed twice, while wearing two different soft multifocal contact lenses in one eye.
The order in which the participant wears each of the multifocal contact lenses for these tasks will be randomized.
After the assessment while wearing the first multifocal lens is completed, subjects will repeat the task while wearing the second multifocal lens.
|
Proclear 1 day is a commercially available single vision soft contact lens for single use (daily wear).
Participants will wear these contacts at the beginning of the study visit to establish best corrected vision.
Participants will then continue to wear this contact lens in one eye for the duration of the study visit.
MyDay is a commercially available multifocal soft contact lens for daily wear.
Adult participants will assess images for ghosting while wearing a MyDay contact lens in one eye.
Order of exposure to this lens will be determined via randomization.
NaturalVue is a commercially available multifocal soft contact lens for daily wear.
Adult participants will assess images for ghosting while wearing a NaturalVue contact lens in one eye.
Order of exposure to this lens will be determined via randomization.
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.)
|
|
Aktywny komparator: Children: Lens 3, then Lens 4
Subjects will be asked to look at letters and describe any shadows or distortions they see using slider bars or numerical rating scales.
This will be performed twice, while wearing two different soft multifocal contact lenses in one eye.
The order in which the participant wears each of the multifocal contact lenses for these tasks will be randomized.
After the assessment while wearing the first multifocal lens is completed, subjects will repeat the task while wearing the second multifocal lens.
|
Proclear 1 day is a commercially available single vision soft contact lens for single use (daily wear).
Participants will wear these contacts at the beginning of the study visit to establish best corrected vision.
Participants will then continue to wear this contact lens in one eye for the duration of the study visit.
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.)
MiSight 1 Day is a commercially available multifocal soft contact lens for daily wear.
Children participants will assess images for ghosting while wearing a MiSight 1 Day contact lens in one eye.
Order of exposure to this lens will be determined via randomization.
An investigational multifocal soft contact lens for daily wear.
While the contact lens is made of an FDA approved material which is already marketed in the United States, it differs from commercially available lenses in that it has a slightly different optical design.
Children participants will assess images for ghosting while wearing this investigational contact lens in one eye.
Order of exposure to this lens will be determined via randomization.
|
|
Aktywny komparator: Children: Lens 4, then Lens 3
Subjects will be asked to look at letters and describe any shadows or distortions they see using slider bars or numerical rating scales.
This will be performed twice, while wearing two different soft multifocal contact lenses in one eye.
The order in which the participant wears each of the multifocal contact lenses for these tasks will be randomized.
After the assessment while wearing the first multifocal lens is completed, subjects will repeat the task while wearing the second multifocal lens.
|
Proclear 1 day is a commercially available single vision soft contact lens for single use (daily wear).
Participants will wear these contacts at the beginning of the study visit to establish best corrected vision.
Participants will then continue to wear this contact lens in one eye for the duration of the study visit.
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.)
MiSight 1 Day is a commercially available multifocal soft contact lens for daily wear.
Children participants will assess images for ghosting while wearing a MiSight 1 Day contact lens in one eye.
Order of exposure to this lens will be determined via randomization.
An investigational multifocal soft contact lens for daily wear.
While the contact lens is made of an FDA approved material which is already marketed in the United States, it differs from commercially available lenses in that it has a slightly different optical design.
Children participants will assess images for ghosting while wearing this investigational contact lens in one eye.
Order of exposure to this lens will be determined via randomization.
|
Co mierzy badanie?
Podstawowe miary wyniku
Podstawowe miary wyniku
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
|
Ghosting Quantification
Ramy czasowe: Day 1
|
Ghosting quantification (e.g. how "doubled" the image looks) will be compared against expected template images and those predicted. Subjects will provide a quality rating of ghosting on a scale between 0 - 100, with lower scores indicating more ghosting of the image and 100 representing an optically perfect image. The VisionApp will also model ghosting measurements for direction, separation, blur and strength into a predictive quality rating, which will be compared to the subject's subjective expected, or overall, quality rating. |
Day 1
|
Współpracownicy i badacze
Tutaj znajdziesz osoby i organizacje zaangażowane w to badanie.
Sponsor
Sponsor
Daty zapisu na studia
Daty te śledzą postęp w przesyłaniu rekordów badań i podsumowań wyników do ClinicalTrials.gov. Zapisy badań i zgłoszone wyniki są przeglądane przez National Library of Medicine (NLM), aby upewnić się, że spełniają określone standardy kontroli jakości, zanim zostaną opublikowane na publicznej stronie internetowej.
Główne daty studiów
Rozpoczęcie studiów (Rzeczywisty)
Rozpoczęcie studiów
10 października 2025
Zakończenie podstawowe (Szacowany)
Zakończenie podstawowe
1 grudnia 2026
Ukończenie studiów (Szacowany)
Ukończenie studiów
1 grudnia 2026
Daty rejestracji na studia
Pierwszy przesłany
Pierwszy przesłany
30 kwietnia 2026
Pierwszy przesłany, który spełnia kryteria kontroli jakości
Pierwszy przesłany, który spełnia kryteria kontroli jakości
30 kwietnia 2026
Pierwszy wysłany (Rzeczywisty)
Pierwszy wysłany
6 maja 2026
Aktualizacje rekordów badań
Ostatnia wysłana aktualizacja (Rzeczywisty)
Ostatnia wysłana aktualizacja
24 sierpnia 2026
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
21 sierpnia 2026
Ostatnia weryfikacja
Ostatnia weryfikacja
1 sierpnia 2026
Więcej informacji
Terminy związane z tym badaniem
Dodatkowe istotne warunki MeSH
Inne numery identyfikacyjne badania
Inne numery identyfikacyjne badania
- 12501b
Plan dla danych uczestnika indywidualnego (IPD)
Planujesz udostępniać dane poszczególnych uczestników (IPD)?
NIE
Informacje o lekach i urządzeniach, dokumenty badawcze
Bada produkt leczniczy regulowany przez amerykańską FDA
Nie
Bada produkt urządzenia regulowany przez amerykańską FDA
Tak
produkt wyprodukowany i wyeksportowany z USA
Nie
Te informacje zostały pobrane bezpośrednio ze strony internetowej clinicaltrials.gov bez żadnych zmian. Jeśli chcesz zmienić, usunąć lub zaktualizować dane swojego badania, skontaktuj się z register@clinicaltrials.gov. Gdy tylko zmiana zostanie wprowadzona na stronie clinicaltrials.gov, zostanie ona automatycznie zaktualizowana również na naszej stronie internetowej .