Exploration Strategies in Night Vision Sensors
STRAT-JVN
1 other identifier
observational
10
0 countries
N/A
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for all trials
Started Feb 2026
Shorter than P25 for all trials
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
September 18, 2025
CompletedFirst Posted
Study publicly available on registry
January 20, 2026
CompletedStudy Start
First participant enrolled
February 1, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 25, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 25, 2026
January 20, 2026
January 1, 2026
11 months
September 18, 2025
January 15, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Eye movements characterized by saccades (speed, latency, and number) for each stimulus
Measurements from eyetracker
Day 1 (Visit 1) and during follow-up visits at Day 2 (Visit 2), Day 3 (Visit 3), and Day 4 (Visit 4)
Head movements (horizontal angle of the participant's head) for each stimulus and throughout the exposure
Measurements extract from motion capture
Day 1 (Visit 1) and during follow-up visits at Day 2 (Visit 2), Day 3 (Visit 3), and Day 4 (Visit 4)
Secondary Outcomes (3)
The average stimulus detection times.
Day 1 (Visit 1) and during follow-up visits at Day 2 (Visit 2), Day 3 (Visit 3), and Day 4 (Visit 4)
Number of correct responses to the perceptual task
Day 1 (Visit 1) and during follow-up visits at Day 2 (Visit 2), Day 3 (Visit 3), and Day 4 (Visit 4)
Visual fatigue will be measured using a questionnaire
Day 1 (Visit 1) and during follow-up visits at Day 2 (Visit 2), Day 3 (Visit 3), and Day 4 (Visit 4)
Eligibility Criteria
French volunteers
You may qualify if:
- 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.
You may not qualify if:
- Pregnant or breastfeeding women;
- Incapacitated adults;
- Individuals who do not understand French (written or spoken).
Contact the study team to confirm eligibility.
Sponsors & Collaborators
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
September 18, 2025
First Posted
January 20, 2026
Study Start
February 1, 2026
Primary Completion (Estimated)
December 25, 2026
Study Completion (Estimated)
December 25, 2026
Last Updated
January 20, 2026
Record last verified: 2026-01