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Randomised controlled trials of the effects of mindfulness integrated into high-intensity interval resistance training on the physical and mental health of healthy adult men

Randomised controlled trials of the effects of mindfulness integrated into high-intensity interval resistance training on the physical and mental health of healthy adult men

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300077030
Enrollment
Unknown
Registered
2023-10-27
Start date
2023-10-21
Completion date
Unknown
Last updated
2025-04-21

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

Conditions

physically and mentally healthy

Interventions

Mindfulness HIIRT group:Mindfulness exercises and high-intensity interval resistance exercises
HIIRT group:high-intensity interval resistance exercises
no-treatment control:none

Sponsors

Sun Yat-sen University
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
17 Years to 30 Years

Inclusion criteria

Inclusion criteria: 1. Healthy male undergraduate or graduate students; 2. Aged 17-30 years old; 3. 18.5 <= BMI < 24 kg/m2.

Exclusion criteria

Exclusion criteria: 1. Regular Mindfulness Practice and Physical Exercise: Participants who have engaged in regular mindfulness practice or physical exercise (in the past three months, without regular exercise habits, participating in moderate-intensity exercise less than three times per week, and each session lasting less than 20 minutes, assessed by the International Physical Activity Questionnaire (IPAQ)) are excluded; 2. Smokers and Drinkers: Smokers (individuals who have smoked continuously or cumulatively for six months or more) and drinkers (males consuming more than 25g of alcohol per day, females consuming more than 15g of alcohol per day) are excluded; 3. Have participated in or are participating in research projects in other projects within the last three months; 4. Those who are about to receive or are receiving medication; 5. No contraindications to exercise testing, such as severe hypertension, heart disease, peripheral vascular disease, respiratory disease, etc., assessed by the Physical Activity Preparation Questionnaire (PAR-Q); 6. Unable to perform physical function tests and answer questionnaire questions correctly; 7. Failure to follow the test procedure; 8. Those who refuse to sign informed consent.

Design outcomes

Primary

MeasureTime frame
HDL function (macrophage cholesterol efflux);

Secondary

MeasureTime frame
Body fat;Body Mass Index;VO2max;Mindfulness;Depression;Anxiety;Pressure;Vital capacity;Height;Weight;Push-up;Crunch;Standing long jump;Sit and Reach;Happiness;Health behavior promotion;

Countries

China

Contacts

Public ContactWang Dongliang

Sun Yat-sen University

wdliang@mail.sysu.edu.cn+86 20 8733 2472

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026