VisionApp - Ghosting
14. Mai 2026 aktualisiert von: 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).
Studienübersicht
Status
Rekrutierung
Bedingungen
Detaillierte Beschreibung
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.
Studientyp
Interventionell
Einschreibung (Geschätzt)
12
Phase
- Unzutreffend
Kontakte und Standorte
Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.
Studienkontakt
- Name: Pete Kollbaum, PhD
- Telefonnummer: 812-555-5500
- E-Mail: kollbaum@iu.edu
Studienorte
-
-
Indiana
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Bloomington, Indiana, Vereinigte Staaten, 47405
- Rekrutierung
- Clinical Optics Research Lab
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Kontakt:
- Pete Kollbaum, PhD
- E-Mail: kollbaum@iu.edu
-
-
Teilnahmekriterien
Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.
Zulassungskriterien
Studienberechtigtes Alter
- Kind
- Erwachsene
- Älterer Erwachsener
Akzeptiert gesunde Freiwillige
Ja
Beschreibung
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
Studienplan
Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Diagnose
- Zuteilung: Zufällig
- Interventionsmodell: Crossover-Aufgabe
- Maskierung: Keine (Offenes Etikett)
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
|---|---|
|
Aktiver 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.)
|
|
Aktiver 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.)
|
|
Aktiver 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.
|
|
Aktiver 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.
|
Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Ghosting Quantification
Zeitfenster: 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
|
Mitarbeiter und Ermittler
Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.
Sponsor
Studienaufzeichnungsdaten
Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.
Haupttermine studieren
Studienbeginn (Tatsächlich)
10. Oktober 2025
Primärer Abschluss (Geschätzt)
1. August 2026
Studienabschluss (Geschätzt)
1. August 2026
Studienanmeldedaten
Zuerst eingereicht
30. April 2026
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
30. April 2026
Zuerst gepostet (Tatsächlich)
6. Mai 2026
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
18. Mai 2026
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
14. Mai 2026
Zuletzt verifiziert
1. Mai 2026
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Zusätzliche relevante MeSH-Bedingungen
Andere Studien-ID-Nummern
- 12501b
Plan für individuelle Teilnehmerdaten (IPD)
Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?
NEIN
Arzneimittel- und Geräteinformationen, Studienunterlagen
Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt
Nein
Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt
Ja
Produkt, das in den USA hergestellt und aus den USA exportiert wird
Nein
Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .
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