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Effect of Indoor Plants on Cardiopulmonary System

Effect of Indoor Plants on Cardiopulmonary System: a Randomized, Crossover, Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06060145
Enrollment
41
Registered
2023-09-29
Start date
2023-12-21
Completion date
2024-03-31
Last updated
2024-07-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiopulmonary

Brief summary

This is a randomized controlled human exposure crossover study, aims to explore the health benefits of indoor plants on cardiopulmonary system on adults.

Detailed description

The researchers will conduct a randomized cross-controlled trial involving 48 healthy adults in Hangzhou, China. These participants will be randomly assigned into two groups, each comprising 24 individuals. Each participant will undergo two separate exposures in an office setting: one exposure without any plants present, and another exposure with 34 to 38 potted plants. A washout period of at least 4 weeks will be implemented between the two exposures. Questionnaires, physical examinations and the collection of biological samples will be conducted prior to exposure and after exposure. In addition, the monitoring of negative air ion, air pollutants and noise exposure, as well as collection of environmental microbial samples, will be conducted on weekdays. Researchers will gather samples of blood, urine, nasal secretion, and exhaled breath condensate from participants.

Interventions

OTHERPlants placed in an office environment

The intervention group will be provided with an intervention consisting of 34-38 potted plants arranged in an office environment for a duration of 8 hours (09:00-17:00) on weekdays (Monday to Friday) for 4 weeks.

OTHERDevoid of any plant presence in an office environment

Participants assigned to the control group will be exposed to an office environment devoid of any plant presence for a duration of 8 hours (09:00-17:00) on weekdays (Monday to Friday) for 4 weeks.

Sponsors

Zhejiang Chinese Medical University
CollaboratorOTHER_GOV
Lina Zhang
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 35 Years
Healthy volunteers
Yes

Inclusion criteria

* Living in Hangzhou during the study period; * Non-smoking, no history of alcohol or drug abuse; * Staying indoors in daytime we required.

Exclusion criteria

* Current or ever smokers; * Subjects with allergic disease, such as allergic rhinitis, allergic asthma, and atopy; * Subjects with cardiovascular disease, such as congenital heart disease, pulmonary heart disease, and hypertension; * Subjects with respiratory disease, such as asthma, chronic bronchitis, and chronic obstructive pulmonary disease; * Subjects with chronic disease, such as diabetes, chronic hepatitis, and kidney disease; * Subjects with a history of major surgery; * Medication use or dietary supplements intake in recent two months; * Unable to cooperate with follow-up.

Design outcomes

Primary

MeasureTime frameDescription
Forced Vital Capacity(FVC)Baseline and after 4 weeks plants exposure in first stage, and after washout period, baseline and after 4 weeks plants exposure in second stage.We plan to measure forced vital capacity (FVC) of lung function.

Secondary

MeasureTime frameDescription
Blood Pressure(BP)Baseline and after 4 weeks plants exposure in first stage, and after washout period, baseline and after 4 weeks plants exposure in second stage.We plan to measure systolic blood pressure (SBP) and diastolic blood pressure (DBP).
Heart Rate Variability(HRV)Baseline and after 4 weeks plants exposure in first stage, and after washout period, baseline and after 4 weeks plants exposure in second stage.We plan to measure Heart Rate Variability (HRV).

Other

MeasureTime frameDescription
C-reactive protein(CRP)Baseline and after 4 weeks plants exposure in first stage, and after washout period, baseline and after 4 weeks plants exposure in second stage.We plan to measure serum concentrations of C-reactive protein(CRP)
Interleukin-6(IL-6)Baseline and after 4 weeks plants exposure in first stage, and after washout period, baseline and after 4 weeks plants exposure in second stage.We plan to measure the serum concentrations of Interleukin-6
Tumor necrosis factor-α(TNF-α)Time Frame: Baseline and after 4 weeks plants exposure in first stage, and after washout period, baseline and after 4 weeks plants exposure in second stage.We plan to measure the serum concentrations of Tumor necrosis factor-α

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026