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Clinical Trials in Switzerland / NCT02919137
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Systematically Assessing Effects of Colored Light on Humans With a Multi-modal Approach (Substudy 7 of 7)

NCT02919137 · tracked via the Priya Life Science Switzerland tracker
Phase
Not applicable
Started
2025-06-01
Last updated
2025-07-29

Condition(s) studied

Exposure to Man-made Visible Light

Investigational drug(s) / intervention(s)

Visible light exposure

Visible light exposure: Subjects will be exposed to visible colored light for 45 minutes. The visible light will be generated by red-green-blue light emitting diodes light cans.

Study summary

NOTE: This is the seventh of in total 7 sub-studies related to the Ethics Committee of the Canton of Bern Ref. No. KEK-BE 2016-00674. This sub-study includes 50 participants and 8 arms, in total 350 participants will be assessed in all 7 sub-studies.

General study information: This is a randomized, cross-over, quantitative study, which investigates physiological variables, mood, and affect of healthy participants in response to colored light exposure. The Participants take part in 5-8 arms and are exposed to colored light only, or are additionally asked to solve cognitive tasks during the colored light exposure. Primary aim is to measure the change in several physiological variables, mood, and affect during colored light exposure of 15 or 45 minutes. The risk for the participants is negligible and comparable to the risk during daily life.

Eligibility

Sex
ALL
Min age
18 Years
Max age
50 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Normal color vision * Right handed * Written informed consent Exclusion Criteria: * Smoking * Any kind of diagnosed sleep disorder or neurological or psychiatric disorder in the last 3 months * Acute severe traumas * Chronic diseases with the necessity for medication * Use of recreational drugs * Regular intake of medication that would affect the outcome measures * Regular excessive alcohol use (\> 18 standard units / week) * Transmeridian travel in the last month (crossed \> 1 time zone border) * Night shift word during the last month

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
University of Bern, Institute of Complementary Medicine Bern Switzerland

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT02919137 on ClinicalTrials.gov ↗ ← All trials in Switzerland