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Mental Health ConditionsNCT07044154

Effect of Sun Tai Chi on the Cardiopulmonary System and Mental Health in University Students

A study testing Tai Chi (Sun Style) and Health lifestyle education in people with Mental Health Conditions and University Students, run by Universidad Católica del Maule at 1 site in Chile.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

Currently, university students face physical and mental health issues, which are reflected in low levels of physical activity, a decline in healthy eating behaviors, and a high prevalence of mental health symptoms such as stress, anxiety, and depression. Read more about this study

Who is it for?
Ages 18 to 29 years
Conditions the study is for
Mental Health Conditions, University Students
What is being tested?
Tai Chi (Sun Style) and Health lifestyle education
Could I receive a placebo?
No, everyone receives an active treatment
How many people
56 participants
Where
1 siteChile
Study dates
1 Jul 2025to 31 Aug 2026
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 29 years
  • All sexes
  • No healthy volunteers
  • Adult

Who may be able to join

  • Undergraduate university students
  • Aged 18 to 29 years
  • Both sexes
  • Present mental health symptoms assessed by the Depression Anxiety Stress Scales - 21 Items (DASS-21) questionnaire, according to cutoff points established by Lovibond et al., ranging from mild to severe in any of the subscales of stress (score 15 to 33), anxiety (score 8 to 19), or depression (score 10 to 27).
  • Report a healthy physical condition suitable for Tai Chi practice (self-reported).

Who cannot join

  • Engage in a high level of physical activity according to the International Physical Activity Questionnaire (IPAQ) or have regularly practiced moderate to high intensity physical activity in the last 3 months.
  • Report chronic illnesses that limit or contraindicate the practice of exercises required in Tai Chi.
  • Present cardiovascular, pulmonary, or neurological diseases.
  • Exhibit either no mental health impairment or severe impairment according to cutoff scores established by Lovibond et al. in the DASS-21 questionnaire (stress subscale score lower than 15 or greater than 33, anxiety subscale score lower than 8 or greater than 19, depression subscale score lower than 10 or greater than 27).
  • Present specific psychiatric diagnoses, such as Attention-Deficit/Hyperactivity Disorder (ADHD), self-reported.
  • Consume medications for mental health treatment.
  • Consume medications or substances that influence cardiac autonomic modulation (e.g., beta-blockers).

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Pamela Campos Rojas, PT contact

+56992117273

pcampos@ucm.cl

Antonio R Zamunér, PhD contact

azamuner@ucm.cl

Chile1 site, 1 recruiting
  • Universidad Católica del Maule

    Talca, Maule Region, 3460000

    Pamela Campos Rojas, PT, +56992117273, pcampos@ucm.cl

    Recruiting

Other trials in Chile

About this study

Official title: Effect of Sun Tai Chi on the Cardiopulmonary System and Mental Health in University Students: A Mixed Randomized Clinical Trial

Currently, university students face physical and mental health issues, which are reflected in low levels of physical activity, a decline in healthy eating behaviors, and a high prevalence of mental health symptoms such as stress, anxiety, and depression. Therefore, it is necessary to develop safe, effective, and sustainable interventions that support comprehensive health and provide formative experiences that reinforce the importance of developing healthy lifestyle habits and self-care.

In this regard, Tai Chi has been shown to offer physical and mental health benefits. Tai Chi is a low- to moderate-intensity exercise with low joint impact, which facilitates the transition from a sedentary to an active lifestyle.

Considering the health problems experienced by university students, it is proposed that a Tai Chi intervention could help produce beneficial effects on both physical and mental health. In this context, the present study aims to implement Tai Chi classes with the objective of determining their effect on the cardiac autonomic system, mental health, and the perception of benefits, facilitators, and barriers among participating university students compared to a control group.

Read the detailed description

In Chile, there are currently over 1.2 million undergraduate university students who exhibit low levels of physical activity and mental health issues such as anxiety and depression. These problems tend to worsen after the first year of higher education, along with the development of unhealthy eating habits and weight gain.

In this context, Tai Chi has shown multiple benefits for overall health. Specifically, the Sun style of Tai Chi is characterized by gentle and accessible movements, making it well-suited to the university setting, and has demonstrated positive effects on both physical and mental health.

Previous studies indicate that regular practice of Tai Chi may positively influence autonomic cardiac control, measured through heart rate variability (HRV), as well as mental health. However, the available evidence is still limited and heterogeneous.

This study aims to evaluate, in university students, the effects of a 6-week Sun Tai Chi program, with 60-minute sessions held twice per week, on the following:

  • Heart Rate Variability (HRV), as a marker of cardiovascular health and stress,
  • Mental health, assessed with the Depression Anxiety Stress Scales - 21 Items (DASS-21 scale),
  • Participants' qualitative perceptions regarding the program's benefits, barriers, and facilitators.

Given the limited research on Tai Chi in university student populations, this study seeks to contribute evidence on its potential comprehensive health benefits in this group.

Being tested
Tai Chi (Sun Style), Health lifestyle education
Keywords
university students, Sun Tai Chi, cardiac autonomic modulation, cardiopulmonary capacity, mental health, qualitative perception
Medical subject headings
Psychological Well-Being

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Tai Chi (Sun Style)Other

    The Sun Tai Chi intervention will be conducted by a Sun Tai Chi instructor with 7 years of teaching experience and will take place in an exercise room at the Catholic University of Maule. The intervention will last for 6 weeks, with a frequency of twice per week, and each class will last 60 minutes. Each session will begin with 10 minutes of warm-up exercises, followed by 20 minutes of basic Sun Tai Chi exercises, including lower limb movements, overall body mobility at a slow pace, precise movements of the hands and feet, and proper body alignment. This will be followed by 20 minutes of practice of the basic movement sequence of Sun Tai Chi (Taolú), and will conclude with 5 minutes of meditation and 5 minutes of relaxation exercises.

  • Health lifestyle educationBehavioural

    The control group will receive guidance on a healthy physical and mental lifestyle.

Study groups in NCT07044154
Study groupRoleWhat they receive
Experimental: Sun Tai Chi GroupExperimentalThe group will participate in 60-minute Sun Tai Chi sessions, held twice per week over a 6-week period.
Receives: Other: Tai Chi (Sun Style)
ControlOtherThe group will receive informational material on healthy lifestyle topics and will not receive the Sun Tai Chi intervention.
Receives: Behavioral: Health lifestyle education

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. DASS-21 stress

    Stress will be measured using the stress subdomain of the DASS-21, which ranges from 0 to 21 points, with higher scores indicating higher levels of stress.

    Measured: Initial evaluation: Prior to the intervention (week 0) Final evaluation: After 6 weeks of intervention

  2. DASS-21 anxiety

    Anxiety will be measured using the anxiety subdomain of the DASS-21, which ranges from 0 to 21 points, with higher scores indicating higher levels of anxiety.

    Measured: Initial evaluation: Prior to the intervention (week 0) Final evaluation: After 6 weeks of intervention

  3. DASS-21 depression

    Depression will be measured using the depression subdomain of the DASS-21, which ranges from 0 to 21 points, with higher scores indicating higher levels of depression.

    Measured: Initial evaluation: Prior to the intervention (week 0) Final evaluation: After 6 weeks of intervention

  4. Low frequency (LF)

    LF (ms2) is an index of parasympathetic and sympathetic cardiac autonomic modulation derived from the analysis of RR intervals (iRR).

    Measured: Initial evaluation: Prior to the intervention (week 0) Final evaluation: After 6 weeks of intervention

  5. High frequency (HF)

    HF (ms2) is an index of parasympathetic cardiac autonomic modulation derived from the analysis of RR intervals (iRR).

    Measured: Initial evaluation: Prior to the intervention (week 0) Final evaluation: After 6 weeks of intervention

  6. Low frequency/Hight frequency ratio (LF/HF)

    LF/HF is an index reflecting the balance between the parasympathetic and sympathetic cardiac autonomic modulation derived from the analysis of RR intervals (iRR).

    Measured: Initial evaluation: Prior to the intervention (week 0) Final evaluation: After 6 weeks of intervention

  7. Pattern with no variation (0V)

    0V (%) is a pattern quantified through symbolic analyses of the RR intervals (iRR) reflecting the sympathetic cardiac modulation.

    Measured: Initial evaluation: Prior to the intervention (week 0) Final evaluation: After 6 weeks of intervention

  8. Pattern with two unlike variation (2ULV)

    2ULV (%) is a pattern quantified through symbolic analyses of the RR intervals (iRR) reflecting the parasympathetic cardiac modulation.

    Measured: Initial evaluation: Prior to the intervention (week 0) Final evaluation: After 6 weeks of intervention

  9. Baroreflex sensitivity (BRS)

    Baroreflex sensitivity is an index that assesses the heart rate response to changes in blood pressure and serves as an indicator of cardiovascular health.

    Measured: Time Frame: Initial evaluation: Prior to the intervention (week 0) Final evaluation: After 6 weeks of intervention

  10. LFSAP

    The low-frequency index of systolic arterial pressure (LFSAP) reflects the vascular sympathetic autonomic modulation.

    Measured: Time Frame: Initial evaluation: Prior to the intervention (week 0) Final evaluation: After 6 weeks of intervention

  11. Qualitative perception

    The qualitative perception of the participants will consider the perceived benefits, barriers, and facilitators. Data will be collected through semi-structured interviews and focus groups, using a qualitative approach.

    Measured: It will be conducted one week after the last Tai Chi class.

Secondary outcomes (1)
  1. VO2 Peak

    Peak oxygen uptake (VO2 peak mL/kg/min) measured during a symptom-limited graded cardiopulmonary exercise test (CPET) on a treadmill or cycle ergometer, representing the highest volume of oxygen consumed during the test.

    Measured: Initial evaluation: Prior to the intervention (week 0) Final evaluation: After 6 weeks of intervention

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted29 Jun 2025
  2. Study start1 Jul 2025
  3. Primary completion31 Jul 2026 (estimated)
  4. Study completion31 Aug 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
A randomized clinical trial will be conducted, using a mixed quantitative-qualitative phenomenological design, single-blind, prospective longitudinal, with non-probabilistic convenience sampling. First, the quantitative phase will be carried out, followed by the qualitative phase. Once the Tai Chi intervention is completed (beginning one week after the final session), the qualitative phase will begin.
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
56 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07044154
Sponsor's protocol ID
90/2025
Status last verified
Apr 2026
First submitted
12 Jun 2025
Last updated
29 Apr 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Tai Chi (Sun Style) and Health lifestyle education in people with Mental Health Conditions and University Students, run by Universidad Católica del Maule at 1 site in Chile.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 7 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 29 Apr 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Chile. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Pamela Campos Rojas, PT (+56992117273, pcampos@ucm.cl), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

DASS-21 stress (time frame: Initial evaluation: Prior to the intervention (week 0) Final evaluation: After 6 weeks of intervention). The study lists 11 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 29 Apr 2026.

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