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Not yet recruitingNCT02919189Updated Jan 14, 2026

Systematically Assessing Effects of Colored Light on Humans With a Multi-modal Approach (Substudy 5 of 7)

An interventional study of Visible light exposure in Exposure to Man-made Visible Light, sponsored by University of Bern. Not yet recruiting at 1 site in Switzerland. Open to participants aged 18 Years to 50 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-01-14.

Sponsored by University of Bern · Not applicable, Interventional, and Basic science

Phase
Not applicable
Study type
Interventional
Enrollment
50
Allocation
Randomized
Ages
18 Years to 50 Years
Sex
All
01

Study summary

NOTE: This is the fifth 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.

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Conditions studied

  • Exposure to Man-made Visible Light

Keywords

  • cerebral oxygen metabolism
  • functional near-infrared spectroscopy
  • partial pressure of carbon dioxide
  • heart rate variability
  • blood pressure
  • affect
  • mood
  • respiration
  • systematic randomized cross-over study
  • systemic physiology
  • electro-dermal activity
  • pulse-respiratory quotient
03

In context

Respiratory Aspiration

1,092 studies on the registry are indexed under Respiratory Aspiration; 216 are open to participants now.

This study's planned enrollment of 50 is above the median of 42 across 881 interventional studies indexed under Respiratory Aspiration.

Browse Respiratory Aspiration studies →

Lead sponsor

University of Bern is the lead sponsor of 207 studies on the registry; 47 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 50 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Normal color vision
  • Right handed
  • Written informed consent

Exclusion criteria

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
05

Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Randomized
Intervention model
Crossover assignment
Masking
Single (Outcomes assessor)
Enrollment
50 participants (estimated)

Study arms

  • Experimental
    Visible light exposure Red 30 lux

    The participants will be exposed to red fluorescent light at a illuminance of 30 lux at eye level for 15 minutes. The colored light exposure will be preceded by sitting 8 minutes in darkness and followed by sitting 20 minutes in darkness.

    Other: Visible light exposure

  • Experimental
    Visible light exposure Red 120 lux

    The participants will be exposed to red fluorescent light at a illuminance of 120 lux at eye level for 15 minutes. The colored light exposure will be preceded by sitting 8 minutes in darkness and followed by sitting 20 minutes in darkness.

    Other: Visible light exposure

  • Experimental
    Visible light exposure Blue 30 lux

    The participants will be exposed to blue fluorescent light at a illuminance of 30 lux at eye level for 15 minutes. The colored light exposure will be preceded by sitting 8 minutes in darkness and followed by sitting 20 minutes in darkness.

    Other: Visible light exposure

  • Experimental
    Visible light exposure Blue 120 lux

    The participants will be exposed to blue fluorescent light at a illuminance of 120 lux at eye level for 15 minutes. The colored light exposure will be preceded by sitting 8 minutes in darkness and followed by sitting 20 minutes in darkness.

    Other: Visible light exposure

  • Experimental
    Visible light exposure Green 30 lux

    The participants will be exposed to green fluorescent light at a illuminance of 30 lux at eye level for 15 minutes. The colored light exposure will be preceded by sitting 8 minutes in darkness and followed by sitting 20 minutes in darkness.

    Other: Visible light exposure

  • Experimental
    Visible light exposure Green 120 lux

    The participants will be exposed to green fluorescent light at a illuminance of 120 lux at eye level for 15 minutes. The colored light exposure will be preceded by sitting 8 minutes in darkness and followed by sitting 20 minutes in darkness.

    Other: Visible light exposure

  • Experimental
    Visible light exposure White 30 lux

    The participants will be exposed to white fluorescent light at a illuminance of 30 lux at eye level for 15 minutes. The colored light exposure will be preceded by sitting 8 minutes in darkness and followed by sitting 20 minutes in darkness.

    Other: Visible light exposure

  • Experimental
    Visible light exposure White 120 lux

    The participants will be exposed to white fluorescent light at a illuminance of 120 lux at eye level for 15 minutes. The colored light exposure will be preceded by sitting 8 minutes in darkness and followed by sitting 20 minutes in darkness.

    Other: Visible light exposure

Interventions

  • OtherVisible light exposure

    Subjects will be exposed to visible colored light for 15 minutes. The visible light will be generated by fluorescent light lamps.

06

What researchers measure

Primary outcomes

  1. Change in cerebral tissue oxygen saturation during colored light exposure compared with a baseline and a recovery period

    Time frame: 43 minutes (8 min baseline, 15 min colored light exposure, 20 min recovery)

  2. Change in cerebral hemoglobin concentration during colored light exposure compared with a baseline and a recovery period

    Time frame: 43 minutes (8 min baseline, 15 min colored light exposure, 20 min recovery)

  3. Change in variables of the heart rate variability during colored light exposure compared with a baseline and a recovery period

    Time frame: 43 minutes (8 min baseline, 15 min colored light exposure, 20 min recovery)

  4. Change in electro-dermal activity during colored light exposure compared with a baseline and a recovery period

    Time frame: 43 minutes (8 min baseline, 15 min colored light exposure, 20 min recovery)

  5. Change of the blood pressure during colored light exposure compared with a baseline and a recovery period

    Time frame: 43 minutes (8 min baseline, 15 min colored light exposure, 20 min recovery)

  6. Change of the partial pressure of carbon dioxide during colored light exposure compared with a baseline and a recovery period

    Time frame: 43 minutes (8 min baseline, 15 min colored light exposure, 20 min recovery)

  7. Change of the respiration rate during colored light exposure compared with a baseline and a recovery period

    Time frame: 43 minutes (8 min baseline, 15 min colored light exposure, 20 min recovery)

  8. Change of the heart rate during colored light exposure compared with a baseline and a recovery period

    Time frame: 43 minutes (8 min baseline, 15 min colored light exposure, 20 min recovery)

  9. Change of the pulse-respiratory quotient during colored light exposure compared with a baseline and a recovery period

    The pulse-respiratory quotient will be calculated as heart rate divided by the respiration rate.

    Time frame: 43 minutes (8 min baseline, 15 min colored light exposure, 20 min recovery)

  10. Change of the arterial oxygen saturation during colored light exposure compared with a baseline and a recovery period

    Time frame: 43 minutes (8 min baseline, 15 min colored light exposure, 20 min recovery)

07

Study locations

1 site
  • University of Bern, Institute of Complementary Medicine
    Bern, 3012, Switzerland
    • Ursula Wolf, Prof. Dr. · Contact
08

References and documents

Publications

  • Weinzirl J, Wolf M, Nelle M, Heusser P, Wolf U. Colored light and brain and muscle oxygenation. Adv Exp Med Biol. 2012;737:33-6. doi: 10.1007/978-1-4614-1566-4_5. No abstract available. PubMed 22259078 ↗
  • Weinzirl J, Wolf M, Heusser P, Nelle M, Wolf U. Effects of changes in colored light on brain and calf muscle blood concentration and oxygenation. ScientificWorldJournal. 2011 Jun 9;11:1216-25. doi: 10.1100/tsw.2011.118. PubMed 21666991 ↗

Individual participant data

Plan to share: Undecided — Access to research data and documents will be handled according to the Manifesto to advance Data Access and Research Transparency (DART) in Switzerland, formulated at the workshop on "Improving DART in Switzerland" in Bern, November 7th, 2014.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 14, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT02919189
Lead sponsor
University of Bern
Responsible party
Sponsor
First posted
Sep 29, 2016
Start date
Dec 1, 2027 (estimated)
Primary completion
Jul 31, 2028 (estimated)
Completion
Jul 31, 2029 (estimated)
Last update
Jan 14, 2026

Study contacts

Ursula Wolf, Prof. Dr.
Contact
ursula.wolf@ikom.unibe.ch
+41 31 631 8140
Ursula Wolf, Prof. Dr.
principal investigator · University of Bern

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Jan 2026. You cannot join it, but the record below documents what was studied.

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