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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02882542
Other study ID # COLOR10_c
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 1, 2018
Est. completion date August 30, 2021

Study information

Verified date September 2021
Source University of Bern
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

NOTE: This is the third 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 6 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.


Recruitment information / eligibility

Status Completed
Enrollment 41
Est. completion date August 30, 2021
Est. primary completion date August 20, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 50 Years
Eligibility 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

Study Design


Related Conditions & MeSH terms

  • Exposure to Man-made Visible Light

Intervention

Other:
Visible light exposure
Subjects will be exposed to visible colored light for 15 minutes. The visible light will be generated by red-green-blue light emitting diodes light cans.

Locations

Country Name City State
Switzerland University of Bern, Institute of Complementary Medicine Bern

Sponsors (1)

Lead Sponsor Collaborator
University of Bern

Country where clinical trial is conducted

Switzerland, 

References & Publications (2)

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. — View Citation

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. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Change in cerebral tissue oxygen saturation during colored light exposure compared with a baseline and a recovery period 43 minutes (8 min baseline, 15 min colored light exposure, 20 min recovery)
Primary Change in cerebral hemoglobin concentration during colored light exposure compared with a baseline and a recovery period 3 hemoglobin concentrations will be analyzed: of oxygenated hemoglobin, of deoxygenated hemoglobin, and of total hemoglobin. 43 minutes (8 min baseline, 15 min colored light exposure, 20 min recovery)
Primary Change in variables of the heart rate variability during colored light exposure compared with a baseline and a recovery period Heart rate variability variables are: the standard deviation of the NN intervals (SDNN), the square root of the mean of the sum of the squares of differences between adjacent NN intervals (RMSSD), the power of the high-frequency component (HF, 0.15-0.4 Hz), the power of the low-frequency component (LF, 0.04-0.15 Hz), the power of the very low-frequency component (VLF, <0.04 Hz), normalized LF and HF components, and the LF/HF ratio. 43 minutes (8 min baseline, 15 min colored light exposure, 20 min recovery)
Primary Change in variables of the electro-dermal activity during colored light exposure compared with a baseline and a recovery period The tonic and phasic parts of the electro-dermal activity will be analyzed. 43 minutes (8 min baseline, 15 min colored light exposure, 20 min recovery)
Primary Change of the blood pressure during colored light exposure compared with a baseline and a recovery period The systolic, diastolic, and mean arterial pressure will be analyzed. 43 minutes (8 min baseline, 15 min colored light exposure, 20 min recovery)
Primary Change of the partial pressure of carbon dioxide during colored light exposure compared with a baseline and a recovery period The partial pressure of carbon dioxide will be assessed by the end-tidal partial pressure of carbon dioxide of the exhalation air. 43 minutes (8 min baseline, 15 min colored light exposure, 20 min recovery)
Primary Change of the respiration rate during colored light exposure compared with a baseline and a recovery period 43 minutes (8 min baseline, 15 min colored light exposure, 20 min recovery)
Primary Change of the heart rate during colored light exposure compared with a baseline and a recovery period 43 minutes (8 min baseline, 15 min colored light exposure, 20 min recovery)
Primary 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. 43 minutes (8 min baseline, 15 min colored light exposure, 20 min recovery)
Primary Change of the arterial oxygen saturation during colored light exposure compared with a baseline and a recovery period 43 minutes (8 min baseline, 15 min colored light exposure, 20 min recovery)
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