- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03558698
Are Cognition and Sleep Affected by Exposure to Carbon Dioxide and Bio Effluents During Sleep?
Danish: Projekt God-Nat. Et Studie af søvnmiljøets Betydning for børns indlæringsevne English: Good Night: A Study of the Impact of the Sleep Environment on Learning in Children
The aim of the project is to examine whether children's sleep and cognition are affected by exposure to CO2 and other bio effluents during sleep. The participants of the study are 36 children recruited from local schools in Aarhus, Denmark.
The study takes place in the climate chambers at the Department of Public Health, Aarhus University. These chambers allow for experimental testing on humans with advanced exposure generation while avoiding contamination from other sources and controlling temperature, humidity, noise, odor, and light.
The children will be sleeping in the chambers under three different conditions:
- One night of good ventilation with a CO2 level of maximum 800 ppm
- One night of good ventilation with high levels of CO2 (3,000 ppm)
- One night of poor ventilation with high concentrations of CO2 (3000 ppm) and other bio effluents.
The study is a within-group design, and groups of six children will be sleeping in the chambers for three nights (separated by seven days). The different groups of children are exposed to the conditions in a randomized order. The study is double-blinded (of security reasons the persons responsible for CO2 concentrations in the chambers are not blinded).
The study takes place on schools nights. The children arrive at 6 pm and leave for school the morning after. In the evening the children are tested for approximately 30-40 minutes to measure their cognitive performance using CANTAB (Cambridge Neuropsychological Test Automated Battery) on iPads. After completing the test, dinner is served and the children have some spare time before going to bed. During night, the quality of sleep (awake time and different sleep stages) will be monitored using Fitbit devices. Sleep quality will also be evaluated using a short sleep questionnaire. The next morning the cognitive performance of the children will be tested again using CANTAB before the children leave for school.
Our primary hypothesis is that children will perform worse on the cognitive test when exposed to high levels of CO2 and other bio effluents than compared to low levels of CO2 and bio effluents in a well-ventilated room. In addition to that our secondary hypotheses are:
- Children will perform worse on the cognitive test when exposed to high levels of CO2 and other bio effluents than compared to CO2 alone.
- Children will sleep less well in an environment with poor ventilation and high levels of CO2 and other bio effluents compared to sleeping in a well-ventilated room with low levels of CO2.
- Children will sleep less well in an environment with poor ventilation and high levels of CO2 and other bio effluents compared to sleeping in a room with high levels of CO2 alone.
- Children will sleep less well and perform worse on the cognitive test when exposed to high levels of CO2 compared to low levels of CO2.
Study Overview
Status
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Aarhus, Denmark, DK-8000
- Aarhus University, Department of Public Health, Section for Environment, Occupation and Health
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Healthy children or children with a well-treated chronic disease not interfering with cognition and sleep quality
- Being able to accomplish a CANTAB test
- Completed questionnaires of sleep patterns
Exclusion Criteria:
- Unable to spend three nights (separated by seven days) in the climate chambers
- Conditions that prevent safe access to the chambers such as claustrophobia
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: Quadruple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Other: Group 1
|
Good ventilation with a low concentration of CO2
CO2 High and Good ventilation
Poor ventilation with high concentrations of CO2 and bio effluents
|
|
Other: Group 2
|
Good ventilation with a low concentration of CO2
CO2 High and Good ventilation
Poor ventilation with high concentrations of CO2 and bio effluents
|
|
Other: Group 3
|
Good ventilation with a low concentration of CO2
CO2 High and Good ventilation
Poor ventilation with high concentrations of CO2 and bio effluents
|
|
Other: Group 4
|
Good ventilation with a low concentration of CO2
CO2 High and Good ventilation
Poor ventilation with high concentrations of CO2 and bio effluents
|
|
Other: Group 5
|
Good ventilation with a low concentration of CO2
CO2 High and Good ventilation
Poor ventilation with high concentrations of CO2 and bio effluents
|
|
Other: Group 6
|
Good ventilation with a low concentration of CO2
CO2 High and Good ventilation
Poor ventilation with high concentrations of CO2 and bio effluents
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Reaction time (Simple)
Time Frame: 10 hours post start of exposure
|
Reaction time in milliseconds.
Outcome from CANTAB RTI Simple.
|
10 hours post start of exposure
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
CANTAB global composite score
Time Frame: 10 hours post start of exposure
|
CANTAB global composite score = outcomes from CANTAB transformed into a global composite score.
|
10 hours post start of exposure
|
|
Reaction Time (Five-Choice)
Time Frame: 10 hours post start of exposure
|
Reaction time in milliseconds.
Outcome from CANTAB RTI Five-Choice.
|
10 hours post start of exposure
|
|
Sleep efficiency
Time Frame: Sleep measured for 9 hours during exposure in bed from 9 pm to 6 am.
|
Sleep efficiency = Percentage of time in bed spent sleeping.
|
Sleep measured for 9 hours during exposure in bed from 9 pm to 6 am.
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Torben Sigsgaard, Department of Public Health - Institute of Environmental and Occupational Medicine, Aarhus University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 111017
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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