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Exploration Strategies in Night Vision Sensors (STRAT-JVN)

D

Direction Centrale du Service de Santé des Armées

Status

Not yet enrolling

Conditions

Visual Acuity

Study type

Observational

Funder types

Other

Identifiers

NCT07352904
2025-A00047-42

Details and patient eligibility

About

The main objective of this clinical trial is to identify a variation in visual strategy characterized by both head movements and eye movements of healthy volunteers during a target detection task when images simulating night vision goggles (NVG) are presented, compared to a situation in which the images simulate a natural environment.

To highlight changes in environmental scanning with simulated images from NVG, objective measurements will be collected:

  • eye movements characterized by saccades (speed, latency, and number) for each stimulus
  • head movements (horizontal angle of the participant's head) for each stimulus and throughout the exposure

Participants sit facing a screen (9.90 m x 2.10 m) onto which a virtual scene is projected. The objective is to correctly identify, as quickly as possible, a target stimulus (represented by a tank) that may appear in the scene. They must use the directional arrows on a game controller to indicate whether the tank is moving to the left or to the right.

There are four visits involving four viewing conditions in which the task remains the same:

  • With restricted field of view and a normal scene.
  • Without restricted field of view and a scene simulating the vision obtained by NVGs.
  • With restricted field of view and a scene simulating the vision obtained by NVGs.
  • Without restricted field of view and a normal scene. Regarding the content of the scene, half of the tests in each visit involve a so-called poor scene when fog is simulated, or an enriched scene when there is no fog. Each visit lasts approximately one hour and thirty minutes.

Enrollment

10 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Affiliated with social security;
  • Normal vision or vision corrected with lenses (far vision ≤ 0.03 log unit (≥ 9/10) OD/OG/binocular);
  • No current or past ocular or binocular pathology: strabismus or amblyopia;
  • Signed non-objection form.

Exclusion criteria

  • Pregnant or breastfeeding women;
  • Incapacitated adults;
  • Individuals who do not understand French (written or spoken).

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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