The Joint Effect of Air Pollution and Exercise on Cognitive Function

December 6, 2025 updated by: Jianxiu Liu, Tsinghua University
A double-blind randomized controlled trial design is used in this study. A mixed design of 2 (pollution reduction group vs. no pollution reduction group) × 3 (high intensity intermittent exercise [HIIT], moderate intensity of aerobic exercise [MICT] and control group [CONT]) is used. 93 subjects recruited by advertising will be randomly divided into 6 groups: high intensity exercise group (pollution reduction vs no pollution reduction), moderate intensity aerobic exercise group (pollution reduction vs no pollution reduction) and Stretching group (Control) (pollution reduction vs no pollution reduction).

Study Overview

Detailed Description

Environmental intervention program In the pollution reduction groups, the air purification system is used 2 hours before the subjects entered the room to minimize the indoor PM2.5 and PM10.

Exercise intervention program including HIIT, MICT and Stretching (Control) group :

The VO2max of all subjects are measured one week before the experiment. HIIT program: 20 minutes exercise of HIIT (1min of 100% VO2max and 1min of 50% VO2max alternately) and 10 minutes of warm-up and relaxation.

MICT program: 20 minutes exercise of 70-75% VO2max and 10 minutes of warm-up and relaxation.

Stretching control group: 30 minutes of stretching, posture adjustment and rehabilitation courses taught by professional therapists.

Study Type

Interventional

Enrollment (Actual)

93

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

    • Beijing Municipality
      • Beijing, Beijing Municipality, China, 100084
        • Tsinghua University

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

20 years to 30 years (Adult)

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • No regular exercise in the past six months;
  • Healthy people without history of disease;
  • Aged between 20 and 30 years old.

Exclusion Criteria:

  • Professional athletes;
  • Regular exercise in the past six months;
  • People who are injured or have a history of disease in the past six months;
  • People who have a history of taking medicine in the past six months.

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: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Triple

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: High intensity intermittent training
HIIT exercise program: 20 minutes HIIT exercise (1min 100% VO2max and 1min 50% VO2max alternately), and warm-up and relaxation before and after exercise for 10 minutes.
Two types of exercise intervention and control group
Experimental: HIIT with pollution reduction
HIIT program: 20 minutes HIIT exercise (1min 100% VO2max and 1min 50% VO2max alternately), and warm-up and relaxation before and after exercise for 10 minutes; Environmental pollution intervention program: air purification system is used order to reduce the PM2.5 and PM10.
Two types of exercise intervention and control group
Air purification in order to reduce the PM2.5 and PM10
Experimental: Moderate intensity continuous training
MICT program: 20 minutes of 70-75% VO2max exercise and 10 minutes of warm-up and relaxation before and after exercise.
Two types of exercise intervention and control group
Experimental: MICT with pollution reduction
MICT program: 20 minutes of 70-75% VO2max exercise and 10 minutes of warm-up and relaxation before and after exercise; Environmental pollution intervention program: air purification system is used order to reduce the PM2.5 and PM10.
Two types of exercise intervention and control group
Air purification in order to reduce the PM2.5 and PM10
Experimental: Stretch control group
Stretching control group: 30 minutes stretching, posture adjustment and rehabilitation courses is taught by professional therapist.
Two types of exercise intervention and control group
Experimental: Control with pollution reduction

Stretching control group: 30 minutes stretching, posture adjustment and rehabilitation courses is taught by professional therapist.

Environmental pollution intervention program: air purification system is used order to reduce the PM2.5 and PM10.

Two types of exercise intervention and control group
Air purification in order to reduce the PM2.5 and PM10

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change of cognitive function
Time Frame: Before and after acute exercise (about 30 minutes).
Cognitive function measured by computer-based tasks including executive function
Before and after acute exercise (about 30 minutes).
Change of biomarkers
Time Frame: Before and after acute exercise (about 30 minutes).
The cognitive-related biomarkers including brain derived neurotrophic factor
Before and after acute exercise (about 30 minutes).
Change of oxyhemoglobin
Time Frame: Before and after acute exercise (about 30 minutes).
Mearsurement of oxyhemoglobin using fNIRS
Before and after acute exercise (about 30 minutes).
Change of transcriptions
Time Frame: Before and after acute exercise (about 30 minutes).
The molecular response of exercise and environment through the measurement of peripheral blood
Before and after acute exercise (about 30 minutes).
Change of metabonomics
Time Frame: Before and after acute exercise (about 30 minutes).
The molecular response of exercise and environment through the measurement of peripheral blood
Before and after acute exercise (about 30 minutes).
Change of cerebral blood flow
Time Frame: Before and after acute exercise (about 30 minutes).
The blood flow of middle cerebral artery measured by ultrasonic doppler
Before and after acute exercise (about 30 minutes).

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change of cognitive function
Time Frame: Three months (from baseline to the third month)
Cognitive function measured by computer-based tasks including executive function
Three months (from baseline to the third month)
Change of aerobic capacity
Time Frame: Three months (from baseline to the third month)
The aerobic capacity measured by the gas metabolism analyzer
Three months (from baseline to the third month)
Change of cerebral blood flow
Time Frame: Three months (from baseline to the third month)
The blood flow of middle cerebral artery measured by ultrasonic doppler
Three months (from baseline to the third month)
Change of biomarkers
Time Frame: Three months (from baseline to the third month)
The cognitive-related biomarkers including brain derived neurotrophic factor
Three months (from baseline to the third month)
Change of oxyhemoglobin
Time Frame: Three months (from baseline to the third month)
Mearsurement of oxyhemoglobin using functional near infrared spectroscopy
Three months (from baseline to the third month)
Change of metabonomics
Time Frame: Three months (from baseline to the third month)
The molecular response of exercise through the measurement of peripheral blood
Three months (from baseline to the third month)
Change of transcriptions
Time Frame: Three months (from baseline to the third month)
The molecular response of exercise through the measurement of peripheral blood
Three months (from baseline to the third month)

Collaborators and Investigators

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

Investigators

  • Study Director: Qian Di, Sc.D., Wanke School of public health, Tsinghua University
  • Study Chair: Xindong Ma, PhD, Department of physical education, Tsinghua University

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the 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)

November 1, 2020

Primary Completion (Actual)

October 30, 2021

Study Completion (Actual)

December 30, 2021

Study Registration Dates

First Submitted

March 29, 2021

First Submitted That Met QC Criteria

April 1, 2021

First Posted (Actual)

April 2, 2021

Study Record Updates

Last Update Posted (Estimated)

December 15, 2025

Last Update Submitted That Met QC Criteria

December 6, 2025

Last Verified

April 1, 2021

More Information

Terms related to this study

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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