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Eye Movement Behaviour and Pupil Size in Natural Outdoor and Indoor Scenes

T

Technical University of Munich

Status

Enrolling

Conditions

Light Sensitivity

Treatments

Other: Indoor vs. outdoor scenes

Study type

Interventional

Funder types

Other

Identifiers

NCT05971238
MPI-TSCN-2023-NATURALEYE
2023-231-S-KH (Other Identifier)

Details and patient eligibility

About

In this study, the researchers will be using eye tracking and detailed lighting measurements to understand how different types of indoor and outdoor lighting affect the eye movements and pupil sizes of our participants. Participants will be paired up and undergo six eye tracking sessions, split across two appointments. Each appointment will involve viewing either indoor or outdoor scenes, and before each session, participants will spend time adapting to the lighting conditions. Overall, each participant will spend 24 minutes being tracked, and the entire study will take about 2-3 hours to complete. The investigators expect differences in eye movements and pupil size between indoor and outdoor scenes.

Enrollment

24 estimated patients

Sex

All

Ages

18 to 40 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • No previous eye-surgeries or ocular impairments like anisometropia, amblyopia, strabism, cataract, watery eyes or hanging eye lids
  • Normal or corrected-to-normal visual acuity (+3dpt. to -5dpt.)
  • Normal colour vision
  • Normal binocular vision

Exclusion criteria

  • Any use of medications or drugs that influence photosensitivity or the ability to concentrate
  • Excessive alcohol and/or drug use
  • Presence of psychiatric disorders
  • Poor sleep quality
  • Diagnosed with epilepsy

Trial design

Primary purpose

Basic Science

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

24 participants in 1 patient group

Eye-tracking, pupillometry and scene rating indoors & outdoors
Experimental group
Treatment:
Other: Indoor vs. outdoor scenes

Trial contacts and locations

1

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Central trial contact

Alexander Hahn; Manuel Spitschan, PhD

Data sourced from clinicaltrials.gov

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