Are Cognition and Sleep Affected by Exposure to Carbon Dioxide and Bio Effluents During Sleep?

October 10, 2018 updated by: University of Aarhus

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

Study Type

Interventional

Enrollment (Actual)

36

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Aarhus, Denmark, DK-8000
        • Aarhus University, Department of Public Health, Section for Environment, Occupation and Health

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

10 years to 12 years (Child)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

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

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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
  • One night of good ventilation with a CO2 level of maximum 800 ppm
  • One night of good ventilation with high levels of CO2 (3000 ppm)
  • One night of poor ventilation with high concentrations of CO2 (3000 ppm) and other bio effluents (The order of the three conditions are randomized)
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
  • One night of good ventilation with a CO2 level of maximum 800 ppm
  • One night of good ventilation with high levels of CO2 (3000 ppm)
  • One night of poor ventilation with high concentrations of CO2 (3000 ppm) and other bio effluents (The order of the three conditions are randomized)
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
  • One night of good ventilation with High CO2 level of maximum 800 ppm
  • One night of good ventilation with high levels of CO2 (3000 ppm)
  • One night of poor ventilation with high concentrations of CO2 (3000 ppm) and other bio effluents (The order of the three conditions are randomized)
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
  • One night of good ventilation with a CO2 level of maximum 800 ppm
  • One night of good ventilation with high levels of CO2 (3000 ppm)
  • One night of poor ventilation with high concentrations of CO2 (3000 ppm) and other bio effluents (The order of the three conditions are randomized)
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
  • One night of good ventilation with a CO2 level of maximum 800 ppm
  • One night of good ventilation with high levels of CO2 (3000 ppm)
  • One night of poor ventilation with high concentrations of CO2 (3000 ppm) and other bio effluents (The order of the three conditions are randomized)
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
  • One night of good ventilation with a CO2 level of maximum 800 ppm
  • One night of good ventilation with high levels of CO2 (3000 ppm)
  • One night of poor ventilation with high concentrations of CO2 (3000 ppm) and other bio effluents (The order of the three conditions are randomized)
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

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Torben Sigsgaard, Department of Public Health - Institute of Environmental and Occupational Medicine, Aarhus University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

January 23, 2018

Primary Completion (Actual)

June 22, 2018

Study Completion (Actual)

June 22, 2018

Study Registration Dates

First Submitted

May 16, 2018

First Submitted That Met QC Criteria

June 14, 2018

First Posted (Actual)

June 15, 2018

Study Record Updates

Last Update Posted (Actual)

October 11, 2018

Last Update Submitted That Met QC Criteria

October 10, 2018

Last Verified

May 1, 2018

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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