The Influence of Climate and Air Pollution on Physical Activity of Chinese People in Shenyang and Shenzhen

The Influence of Climate and Air Pollution on Physical Activity of Chinese People in Shenyang(41.481175ºN) and Shenzhen(22.324386ºN)

Physical activity (PA) refers to bodily movements that result in a significant increase in energy expenditure due to the contraction of skeletal muscles. Physical inactivity has become a major global public health concern and is currently the fourth leading cause of death worldwide. The World Health Organization (WHO) recommends that adults engage in at least 150 minutes of moderate-intensity physical activity (MPA) or 75 minutes of vigorous-intensity physical activity (VPA) per week.

Although some studies suggest that individual differences in PA may have a genetic basis, PA is generally considered to be largely under voluntary control and influenced by climatic and environmental factors. For instance, extreme temperatures-either hot or cold-can increase health risks and reduce individuals' willingness to engage in physical activity. In addition, air pollution, particularly fine particulate matter (PM2.5), poses serious health risks. Exercising in polluted environments may trigger asthma, cardiovascular, or pulmonary conditions.

Since the Industrial Revolution, fossil fuel emissions have contributed to a global surface temperature increase of approximately 1.1°C, with projections suggesting a further rise of 2.5-2.9°C by the end of the century. At the same time, PM2.5 pollution has become a pressing issue, contributing to an estimated 7 million deaths globally in 2012-over one-third of which occurred in rapidly developing Asian countries.

Given the seasonal and geographic variability in climate and air quality, physical activity levels are likely to be affected accordingly.This study aims to investigate the extent to which climatic and environmental factors influence physical activity levels and intensity.

Study Overview

Status

Recruiting

Detailed Description

This study will be conducted in two cities in China: Shenyang (41.481175°N) and Shenzhen (22.324386°N), with 62 participants recruited from each location. By assessing participants' body composition and physical activity levels, along with the climatic and environmental conditions in both cities, we aim to compare how different climates and environmental exposures influence physical activity.

Participants will be asked to wear a GT3X accelerometer every two months to monitor physical activity levels, and an iButton temperature sensor to record ambient temperature. A total of six measurement rounds will be conducted. Concurrently, atmospheric temperature data will be collected via local weather stations, and PM2.5 data will be obtained from publicly available sources.

Study Type

Observational

Enrollment (Estimated)

124

Contacts and Locations

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

Study Contact

Study Contact Backup

Study Locations

    • Guangdong
      • Shenzhen, Guangdong, China
        • Recruiting
        • Shenzhen Institutes of Advanced Technology, Chinese Academy of Science
        • Contact:
        • Contact:

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

  • Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Probability Sample

Study Population

The study population consisted of healthy individuals. Female participants were neither pregnant nor planning to become pregnant, and none were lactating. All subjects were free from serious illnesses or disabilities that could interfere with the study.

Description

Inclusion Criteria:

  • Aged 18 to 55 years
  • Residing in Shenzhen or Shenyang for the entire year

Exclusion Criteria:

  • Disabilities that limit physical activity
  • Any condition preventing participation in physical activity
  • Pregnant or planning pregnancy during the study period
  • Lactating or planning to lactate during the study period

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

Cohorts and Interventions

Group / Cohort
Subjects in Shenzhen
The investigators planned to recruit 62 subjects in Shenzhen. Shenzhen is located in 22.324386ºN, 114.031040ºE, the south of China, with long summers and short winters, high temperatures and frequent rains. The average annual temperature is 23.3℃. In addition, Shenzhen is a city with good economic and technological development. The investigators will measure the physical activity of subjects, and the Temperature, humidity and PM2.5 data of Shenzhen.
Subjects in Shenyang
The investigators planned to recruit 62 subjects in Shenyang. Shenyang is located in 41.481175ºN, 123.253118ºE, the northeastern of China, with cold winters and warm summers, also has long cold periods. The average annual temperature ranges from 6.2 to 9.7℃. In addition, Shenyang focuses on industrial development. The investigators will measure the physical activity of subjects, and the Temperature, humidity and PM2.5 data of Shenyang.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Physical activity level
Time Frame: Through study completion, every two months across 6 assessment rounds, up to 12 months per participant
Physical activity in vector magnitude counts will be recorded using GT3X accelerometer worn near the hip for a consecutive period of 7 days. The monitor should not be worn while bathing or swimming.
Through study completion, every two months across 6 assessment rounds, up to 12 months per participant

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Temperature
Time Frame: Through study completion, an average of 2 years
Temperature in degrees Celsius will be collected using the HOBO mini-weather station.
Through study completion, an average of 2 years
Humidity
Time Frame: Through study completion, an average of 2 years
Humidity in %RH will be collected using the HOBO mini-weather station.
Through study completion, an average of 2 years
Subject exposure to environmental temperature
Time Frame: Through study completion, every two months across 6 assessment rounds, up to 12 months per participant
Exposure temperature in degrees Celsius will be measured by Ibutton. The Ibutton (DS1921G) monitors will be provided for the assessment of both indoor and outdoor temperature of their living environment. The iButtons be affixed to the hand bag to measure the subject exposure temperature.
Through study completion, every two months across 6 assessment rounds, up to 12 months per participant
PM2.5
Time Frame: Through study completion, an average of 2 years
PM2.5 in μg/m3 will be collected through open data website.
Through study completion, an average of 2 years
Sunshine duration
Time Frame: Through study completion, an average of 2 years
Sunshine duration in hours will be collected through open data website.
Through study completion, an average of 2 years
Height
Time Frame: Through study completion, every two months across 6 assessment rounds, up to 12 months per participant
Height in centimeters will be measured by Leicester stadiometer (Seca 217, Germany) to the nearest 0.1cm. Subjects wearing no shoes.
Through study completion, every two months across 6 assessment rounds, up to 12 months per participant
Body Weight
Time Frame: Through study completion, every two months across 6 assessment rounds, up to 12 months per participant
Subjects will be asked to fast overnight and weight in kilograms will be measured using a calibrated Seca body weight scale first thing in the morning on subjects wearing light clothes and no shoes.
Through study completion, every two months across 6 assessment rounds, up to 12 months per participant
Fat percentage
Time Frame: Through study completion, every two months across 6 assessment rounds, up to 12 months per participant
Fat percentage in percentage will be measured using Bioimpedance Analysis (Tanita, MC-980).
Through study completion, every two months across 6 assessment rounds, up to 12 months per participant
Fat mass
Time Frame: Through study completion, every two months across 6 assessment rounds, up to 12 months per participant
Fat mass in kilograms will be measured using Bioimpedance Analysis (Tanita, MC-980).
Through study completion, every two months across 6 assessment rounds, up to 12 months per participant
Fat-free mass
Time Frame: Through study completion, every two months across 6 assessment rounds, up to 12 months per participant
Fat-free mass in kilograms will be measured using Bioimpedance Analysis (Tanita, MC-980).
Through study completion, every two months across 6 assessment rounds, up to 12 months per participant
Muscle mass
Time Frame: Through study completion, every two months across 6 assessment rounds, up to 12 months per participant
Muscle mass in kilograms will be measured using Bioimpedance Analysis (Tanita, MC-980).
Through study completion, every two months across 6 assessment rounds, up to 12 months per participant

Collaborators and Investigators

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

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)

August 1, 2024

Primary Completion (Estimated)

August 31, 2026

Study Completion (Estimated)

August 31, 2026

Study Registration Dates

First Submitted

August 11, 2025

First Submitted That Met QC Criteria

April 8, 2026

First Posted (Actual)

April 13, 2026

Study Record Updates

Last Update Posted (Actual)

April 13, 2026

Last Update Submitted That Met QC Criteria

April 8, 2026

Last Verified

March 1, 2026

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • SIAT-IRB-240415-H0888

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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