Maastricht University
Maastricht, Limburg, 6229ER, Netherlands
NCT Number: NCT06380582
Study design: A cross-over single-blinded treatment design will be used. Participants will undergo 4 different conditions: (1) low air flow and 23°C, (2) low air flow and 35°C, (3) high air flow and 23°C, and (4) high air flow and 35°C. Participants will be blinded to the air quality level; however, it is not possible to blind them to the temperature condition, as they will be able to perceive it as different.
Study population: The population consists of healthy young and middle-aged adults of both sexes between 18 and 40 years.
Intervention (if applicable): Each participant undergoes 4 conditions in randomized order. Two conditions consist of poor air quality defined as 3,000 ppm carbon dioxide and 23°C or 35°C temperature, respectively.
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Notify Me18 year–40 year
All sexes
Interventional
Not applicable
Maastricht, Limburg, 6229ER, Netherlands
Objective: This study aims to examine the effect of indoor air quality and temperature on human cognitive performance. The main research objective of this study is to examine how indoor air quality and temperature affects cognitive performance, respectively. As a secondary objective, it will be examined if a higher temperature of 35°C compared to 23°C amplifies the negative effect of low air flow vs. high air flow on cognitive performance. It will also be examined if human perceive the air quality as less pleasant under the higher temperature, even if the air quality itself does not change in terms of carbon dioxide concentration. Also, the physiological reaction towards poor air quality and elevated temperature will be examined in isolation and interaction.
Main study parameters/endpoints: The main study parameters are the achieved scores of the cognition test, mainly derived from the Cambridge Neuropsychological Test Automated Battery (CANTAB) and the Cognitive Ability Task. As secondary outcome, the physiological response will be examined. Specifically, it will be investigated how the air quality and temperature affect the following physiological parameters: Capillary blood CO2 and pH level, salivary cortisol and a-amylase and serum cytokine response, lung function, heart rate, respiration rate, skin temperature, core temperature, blood pressure, physical activity, and metabolic rate.
Primary Objective: The main research objective of this study is to examine how poor indoor air quality in terms of low air flow compared to high air flow and elevated temperature of 35°C compared to 23°C affect cognitive performance, respectively.
Secondary Objective(s): The following secondary objectives will be investigated in this study:
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Participants, who do not want to be informed about unexpected medical findings, or do not wish that their treating physician will be informed, cannot participate in this study
23C 40%Relative Humidity (RH) low airflow, 23C 40%RH high airflow, 35C 40%RH low airflow, 35C 40% high airflow
Time frame: 1 month
Cambridge Neuropsychological Test Automated Battery (CANTAB) once at 11am and once at 230pm
Time frame: 1 month
Cognitive Ability Task - once at 4pm
Time frame: 1 month
Using a wearable heart rate belt for beat by beat
Time frame: 1 month
Omnical system with a minute frequency
Time frame: 1 month
Using an automate blood pressure cuff every hour
Time frame: 1 month
Blood drawn for future analysis 4 times every 2 hours
Time frame: 1 month
Saliva collected for future analysis 4 times every 2 hours
Time frame: 1 month
Spirometer used 4 times every 2 hours
Time frame: 1 month
Room temperature using an environmental sensor
Time frame: 1 month
Relative Humidity using an environmental sensor
Time frame: 1 month
Carbon dioxide using an environmental sensor
Maastricht University Medical Center
Other
Acronym: AEOLUS
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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