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Effect of Short-term Portable Air Purifier Use on Occupant Health Indicators

Not Applicable
Completed
Conditions
Non-smoking, Healthy Adults
Interventions
Device: Sham-Washout-True Air Filtration Intervention
Device: True-Washout-Sham Air Filtration Intervention
Registration Number
NCT02736487
Lead Sponsor
Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine
Brief Summary

The purpose of this research project is to examine whether short-term use of portable air pollution filtration can result in changes in indoor airborne pollutants and impact on cardiovascular and respiratory health outcomes of the inhabitants.

Detailed Description

This study will focus on evaluating the short-term benefits of a common portable air purifier technology in reducing air pollutant exposure and the anticipated concomitant health impacts. High ambient levels of various air pollutants in the Shanghai area serve as a useful model to test the portable air purifier intervention in a realistic setting. As most people using a portable air purifier would only be able to do so in their residences, the investigators have designed our study only to test residential air purifier use. Our hypothesis is that the reduction in pollutant concentrations in indoor air caused by the air purifier will result in measurable reductions in risk factors for cardiovascular and respiratory diseases.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
72
Inclusion Criteria
  • Healthy, non-smoking adults
  • Live in the dormitory building at Shanghai First People's Hospital (South Section).
Exclusion Criteria
  • Current smokers
  • Has any of the following diseases: chronic respiratory, cardiovascular, liver, renal, hematological disease; diabetes mellitus;
  • Has any other diseases that may confound or complicate the effects of the intervention
  • Pregnant females

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
Group B: Sham-Washout-TrueSham-Washout-True Air Filtration InterventionSubjects in group B receives sham air filtration intervention, then at least two weeks of washout period, followed by true air filtration intervention.
Group A: True-Washout-ShamTrue-Washout-Sham Air Filtration InterventionSubjects in group A receives true air filtration intervention, then at least two weeks of washout period, followed by sham air filtration intervention.
Primary Outcome Measures
NameTimeMethod
Change from baseline R5 (airway resistance measured at 5Hz) within 2h after the filtration interventionWithin 2h after the filtration intervention

R5 (airway resistance measured at 5Hz) was accessed by impulse oscillometry in all subjects within 2h after the filtration intervention to compare to the R5 value of study subjects at baseline (i.e. before the start of intervention).

Change in baseline exhaled nitric oxide (eNO) within 2h after the filtration interventionWithin 2h after the filtration intervention

Exhaled nitric oxide (eNO) was measured in all subjects within 2h after the filtration intervention to compare to the exhaled nitric oxide measurement of study subjects at baseline (i.e. before the start of intervention). Exhaled breath is collected in air sampling bags, and the concentration of NO was quantified by Thermo Scientific model 42i (NO-NO2-NOx) analyzer.

Change from baseline PWV (pulse wave velocity) within 2h after the filtration interventionWithin 2h after the filtration intervention

PWV (pulse wave velocity) was measured by the VICORDER instrument in all subjects right after filtration intervention to compare to the PWV value measured at baseline (i.e. before the start of intervention).

Change in exhaled nitric oxide (eNO) at 6h after filtration intervention compared to baseline6h after filtration intervention

Exhaled nitric oxide (eNO) was measured in all subjects 6h after filtration intervention to compare to the exhaled nitric oxide measurement of study subjects at baseline (i.e. before the start of intervention). Exhaled breath is collected in air sampling bags, and the concentration of NO was quantified by Thermo Scientific model 42i (NO-NO2-NOx) analyzer.

Change from baseline FEV1 (forced expiratory volume in the first second of exhalation) within 2h after the filtration interventionWithin 2h after the filtration intervention

FEV1 (forced expiratory volume in the first second of exhalation, unit: liter) was measured by spirometry in all subjects within 2h after the filtration intervention to compare to FEV1 value of study subjects at baseline (i.e. at start of the study).

Secondary Outcome Measures
NameTimeMethod
Change in baseline urinary biomarkers of inflammation and oxidative stress at 24h after filtration intervention24h after filtration intervention

Urine samples were collected from each subject at 24h after filtration intervention to quantify changes in urinary oxidative stress and inflammation biomarkers compared to baseline (i.e. before intervention). The urinary biomarkers to be analyzed include: malondialdehyde (MDA), 8-hydroxy-2' -deoxyguanosine (8-OHdG) and creatinine. The unit of the urinary biomarkers will be reported as micro molar/ milliliter.

Change in the duration of deep sleep on the first night and the second night of study participationOn the first night and the second night of study participation

Duration of deep sleep was monitored by a sensor in a wristband on the first night and the second night of study participation

Change from baseline urinary biomarkers of inflammation and oxidative stress at 0h after the filtration interventionAt 0h after the filtration intervention

Urine samples were collected from each subject at 0h after the filtration intervention to quantify changes in urinary oxidative stress and inflammation biomarkers compared to baseline (i.e. before intervention). The urinary biomarkers to be analyzed include: malondialdehyde (MDA), 8-hydroxy-2' -deoxyguanosine (8-OHdG) and creatinine. The unit of the urinary biomarkers will be reported as micro molar/ milliliter.

Changes in baseline blood biomarkers of inflammation, oxidative stress and coagulation right after filtration intervention24h after filtration intervention

Blood samples were collected 24h after filtration intervention for comparison of inflammatory and oxidative stress biomarkers to their baseline level (i.e. before the start of filtration intervention). Blood biomarkers that will be analyzed include: P-selectin, c-reactive protein, Von Willebrand factor and fibrinogen. The unit of the blood biomarkers will be reported as micro molar/ milliliter.

Change in baseline urinary biomarkers of inflammation and oxidative stress at 6h after filtration intervention6h after filtration intervention

Urine samples were collected from each subject at 6h after filtration intervention to quantify changes in urinary oxidative stress and inflammation biomarkers compared to baseline (i.e. before intervention). The urinary biomarkers to be analyzed include: malondialdehyde (MDA), 8-hydroxy-2' -deoxyguanosine (8-OHdG) and creatinine. The unit of the urinary biomarkers will be reported as micro molar/ milliliter.

Changes in baseline blood biomarkers of inflammation, oxidative stress and coagulation within 1h after filtration interventionWithin 1h after filtration intervention

Blood samples were collected within 1h after filtration intervention for comparison of inflammatory and oxidative stress biomarkers to their baseline level (i.e. before the start of filtration intervention). Blood biomarkers that will be analyzed include: P-selectin, c-reactive protein, Von Willebrand factor and fibrinogen. The unit of the blood biomarkers will be reported as micro molar/ milliliter.

Trial Locations

Locations (1)

Shanghai First People's Hospital

🇨🇳

Shanghai, Shanghai, China

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