Clinical Research Directory

Browse clinical research sites, groups, and studies.

Sites Groups Studies

Back to Studies

RECRUITING

NCT07440134

Visual and Postural Behavior in Myopic and Non-Myopic Teenagers

Sponsor: Essilor International

View on ClinicalTrials.gov

Summary

The goal of this observational study is to learn whether different types of eyeglasses prescription and different types of lenses change how close teenagers hold objects when looking at them up close. The study includes adolescents who are non-myopic and adolescents who are myopic and wear either single-vision lenses or lenses slowing down myopia progression. The main questions it aims to answer are: Do teenagers in these three groups use different average working distances (eye-to-object distance) during everyday tasks? Does wearing Essilor® Stellest® lenses change working distance compared with wearing single-vision lenses? Researchers will compare the three groups to see if their working distances differ. Participants will: Complete an initial optometric eye examination. Come for a second visit where they perform everyday activities while wearing a motion-capture system that measures how they move and how far they hold objects.

Official title: Comportement Visuo-postural Des Adolescents Myopes et Non Myopes (CALYPSO)

Key Details

Gender

All

Age Range

12 Years - 17 Years

Study Type

INTERVENTIONAL

Enrollment

100

Start Date

2026-04-03

Completion Date

2027-05

Last Updated

2026-04-03

Healthy Volunteers

Yes

Conditions

Teenagers Myopia

Interventions

DEVICE

Ophtalmic measurements

Participants will undergo a standard ophthalmic examination during the initial visit. All procedures are non-invasive, non-ionising, and conducted using devices routinely employed in clinical ophthalmic practice.

BEHAVIORAL

Visuo-postual measurements

The behavioral part of the study consists of a set of tasks designed to assess eye movements and visual behavior in both controlled and ecological conditions. Participants perform everyday activities while eye movements and body motion are recorded using an eye tracker and motion capture systems.

Inclusion Criteria: * Volunteer adolescent, fluent in French, able to follow protocol and read and write * Aged between 12 and 17 years and 6 months * Adolescent with no history, according to the participant and/or their legal representatives, of any pathology, deficit, or disorder that could interfere with visual or cognitive functions. * If the subject wears glasses, they must have an ophthalmic prescription dated within the last year, certifying that a consultation was carried out during the previous year * If the subject wears Essilor® Stellest® 1.0 lenses, they must have worn them for at least two (2) consecutive months prior to inclusion in the study. * If the subject is nearsighted: -6.5D ≤ equivalent sphere ≤ -0.5D with usual correction * If the subject is not nearsighted: -0.5 \< equivalent sphere ≤ +2.5 Exclusion Criteria: * Age ≤ 12 years * Age \> 17 years and 6 months * Pregnant or breastfeeding women (Article L1121-5) * Persons (legal representatives or subjects) deprived of their liberty by a judicial or administrative decision and persons hospitalized without consent pursuant to Articles L. 3212-1 and L. 3213-1 who are not covered by the provisions of Article L. 1121-8 and persons admitted to a health or social care facility for purposes other than research * Participants who are currently excluded from another study * All categories of persons who are particularly protected under French law are excluded from this research (Articles L1121-5 to L1121-9 of the Public Health Code) * Declared neurological deficit, in particular a history of epileptic pathology or sensorimotor coordination disorders, vestibular or cerebellar pathology (e.g., balance disorders) * Severe declared eye disease involving loss of visual field, such as glaucoma, involving loss of acuity and severe discomfort in low-light or overly bright environments, such as retinitis pigmentosa, or declared and treated dry eye syndrome. * Gougerot-Sjögren syndrome or declared dry eye syndrome * Declared aphakia or pseudophakia (intraocular implant) * Declared systemic pathology, medical treatment, or medication with an effect on vision * People with declared muscle paralysis * Binocular vision problems such as amblyopia, strabismus, or nystagmus * Children of employees or employees of Essilor International, Luxottica, GrandVision, and their subsidiaries * Individuals who have undergone previous refractive surgery, have a history of strabismus surgery, or have a history of any type of eye surgery

Locations (1)

Paris Bastille

Paris, France