AzTrials
AzTrials

University StudentsNCT07178275

The Effects of Qigong Exercises on Acute Anxiety, Mood, and Reaction Time Among Occupational Therapy Students

A study testing Baduanjin Qigong and Passive Rest in people with University Students, run by Medipol University.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
Search all trials

Trial summary

The goal of this study is to examine the short-term effects of a single session of Baduanjin Qigong, a traditional mind-body exercise, on anxiety, mood, and reaction time in young adults studying occupational therapy. Read more about this study

Who is it for?
Ages 18 to 25 yearsHealthy volunteers can take part
Conditions the study is for
University Students
What is being tested?
Baduanjin Qigong and Passive Rest
Could I receive a placebo?
No, everyone receives an active treatment
How many people
50 participants
Where
No sites listed yet
Study dates
1 Dec 2025to 12 Dec 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 25 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • Age between 18-25 years
  • Being an undergraduate occupational therapy student at Medipol University
  • No history of chronic disease, psychiatric diagnosis, or condition preventing participation in physical exercise
  • No prior regular participation in Qigong, yoga, or similar mind-body practices
  • Voluntary participation and provision of informed consent

Who cannot join

  • Use of antidepressant or psychotropic medication
  • Acute pain, infection, or chronic cardiorespiratory disease
  • Inability to complete computer-based visual reaction time testing

Trial locations and contacts

No sites are listed yet. Contact the study team or a site near you to ask about taking part.

HÜLYA YAMAN, Master's degree contact

+905419775047

ergoterapisthulya@gmail.com

About this study

Official title: The Effects of Qigong Exercises on Acute Anxiety, Mood, and Reaction Time Among Occupational Therapy Students: A Double-Blind, Crossover-Controlled Intervention Study

The goal of this study is to examine the short-term effects of a single session of Baduanjin Qigong, a traditional mind-body exercise, on anxiety, mood, and reaction time in young adults studying occupational therapy. Baduanjin is a gentle form of Qigong that combines slow and rhythmic movements, breathing awareness, and mental focus. It has been practiced for centuries in China and has recently gained attention worldwide as a complementary therapy for improving mental, physical, and cognitive health.

University students are an important group to study because they often experience high levels of stress due to academic pressure, economic uncertainty, social expectations, and concerns about the future. These factors can increase vulnerability to problems such as anxiety, depression, attention difficulties, and sleep problems. While many studies have explored long-term non-drug interventions, there are still very few trials investigating immediate, short-term benefits of Qigong in young adult populations.

Read more

Previous research has shown that Baduanjin Qigong can reduce stress, anxiety, and depression, while also improving mood and physical health. For example, studies with college students have reported reductions in anxiety and depression, improvements in body mass index, lung function, and overall well-being after regular Baduanjin practice. Meta-analyses suggest that Baduanjin is especially effective in lowering stress compared to other traditional exercises. Some studies even found that just one 60-minute Qigong session can significantly reduce anxiety and improve mood, as measured by standard psychological tools. These findings suggest that Qigong can work not only as a long-term therapy but also as a rapid relief method in stressful situations.

In Turkey, most Qigong studies have focused on older adults or patient groups, showing benefits such as improved balance, reduced risk of falls, and better sleep quality. However, there are almost no experimental studies on the acute (short-term) psychological and cognitive effects of Qigong in young adults. This study aims to fill that gap.

What will happen in this study?

The study will recruit occupational therapy students.

Each participant will attend a single 60-minute Baduanjin session.

The design is double-blind, randomized, and crossover, which means that participants and evaluators will not know which condition they are assigned to, and each participant will experience both the Qigong session and a control condition on different days.

A short "wash-out" period will separate the sessions to ensure accurate results.

What will be measured?

Participants' anxiety, mood, and reaction time will be tested before and after the Qigong session.

Anxiety will be measured using the State-Trait Anxiety Inventory (STAI-Y1).

Mood will be measured using the Profile of Mood States (POMS).

Reaction time will be measured using a computerized test.

Why is this important?

This study will help us understand whether a single Qigong session can provide immediate psychological relief and improve mental focus for university students. If effective, Qigong could be considered a simple, low-cost, and accessible complementary practice to support student well-being in academic and daily life. The findings may also contribute to future health promotion programs targeting young adults.

Being tested
Baduanjin Qigong, Passive Rest

What participants receive

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

  • Baduanjin QigongBehavioural

    A standardized 60-minute Baduanjin Qigong protocol (15 minutes of breathing-focused warm-up, eight movements each lasting 5 minutes, and 10 minutes of breathing-focused closing). The sessions will be conducted by a licensed occupational therapist certified in Qigong.

  • Passive RestBehavioural

    Passive rest refers to a condition in which participants remain seated or lying quietly in a calm environment for a specified period of time, without engaging in any structured physical activity, therapeutic exercise, or cognitive tasks. During this period, external stimuli such as phone use, electronic devices, or reading materials are restricted in order to minimize distraction. The purpose of the passive rest condition is to provide a neutral control state that accounts for the passage of time and environmental factors, allowing valid comparison with the active intervention

Study groups in NCT07178275
Study groupRoleWhat they receive
Qigong, Then RestingExperimentalParticipants first will receive a 60-minute Baduanjin Qigong session led by a licensed occupational therapist certified in Qigong. Qigong session will include gentle physical movements, controlled breathing, and meditative focus, performed in a quiet room under supervision. After a washout period of 1-day, participants will experience resting. In the resting time participants will undergo 60 minutes of passive rest in a quiet room. The use of phones, electronic devices, or any distracting materials will not be permitted.
Receives: Behavioral: Baduanjin Qigong; Behavioral: Passive Rest
Resting, Then QigongExperimentalParticipants first will undergo 60 minutes of passive rest in a quiet room. The use of phones, electronic devices, or any distracting materials will not be permitted. After a washout period of 1-day, participants will experience a 60-minute Baduanjin Qigong session led by a licensed occupational therapist certified in Qigong. The Qigong session will include gentle physical movements, controlled breathing, and meditative focus, performed in a quiet room under supervision.
Receives: Behavioral: Baduanjin Qigong; Behavioral: Passive Rest

What is being measured

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

  1. State Anxiety (STAI-Y1)

    State anxiety (STAI-Y1) will be assessed using the State-Trait Anxiety Inventory, a validated self-report questionnaire. STAI-Y-1 scores range from 0 to 80 and higher scores are indicative of higher levels of state-anxiety

    Measured: Both at the start and end of all interventions within one hour

Secondary outcomes (1)
  1. Mood Profile (POMS)

    Mood states will be measured using the Profile of Mood States (POMS), a standardized psychometric instrument. The Mood Scale is developed to assess short-term mood changes and consists of 65 words and 6 subscales. It is used to determine how participants feel before starting the test.

    Each individual rates the emotion/mood they experience on a Likert scale ranging from 1 ("not at all") to 5 ("extremely"). These 65 words correspond to six subscales: tension-anxiety, depression-dejection, anger-hostility, vigor-activity, fatigue-inertia, and confusion-bewilderment.

    Measured: Both at the start and end of all interventions within one hour

Timeline

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

  1. First posted17 Sep 2025
  2. Study start1 Dec 2025 (estimated)
  3. Primary completion1 Dec 2026 (estimated)
  4. Study completion12 Dec 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
Crossover
Model description
This study is designed as a randomized crossover study. Participants will be randomly assigned into two groups, defined as Group A and Group B. Following baseline assessments, Group A will receive a 60-minute Qigong intervention, while Group B will not receive any intervention and will remain in a resting condition. At the end of this first phase, outcome measures will be collected from both groups. After a one-day washout period to minimize potential carry-over effects, the groups will cross over. In the second phase, Group A will serve as the control with no intervention, while Group B will participate in the 60-minute Qigong session. Outcome measures will again be collected from both groups immediately following this phase.
Masking
Double blind
Who is masked
Participant, Outcomes assessor
Enrolment
50 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07178275
Sponsor's protocol ID
E-10840098-202.3.02-4431
Status last verified
Sep 2025
First submitted
25 Aug 2025
Last updated
17 Sep 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • Kim E, Lee JE, Sohn M. The Application of One-Hour Static Qigong Program to Decrease Needle Pain of Korean Adolescents With Type 1 Diabetes: A Randomized Crossover Design. J Evid Based Complementary Altern Med. 2017 Oct;22(4):897-901. doi: 10.1177/2156587217722473. Epub 2017 Aug 4.

    PubMed 28776413
  • Alkhatib A, Alshikh Ahmad H, Zhang C, Peng W, Li X. Impact of traditional Chinese Baduanjin exercise on menstrual health among international female students studying in China: a randomized controlled trial. Front Public Health. 2024 Feb 7;12:1259634. doi: 10.3389/fpubh.2024.1259634. eCollection 2024.

    PubMed 38384881
  • Luo X, Zhao M, Zhang Y, Zhang Y. Effects of baduanjin exercise on blood glucose, depression and anxiety among patients with type II diabetes and emotional disorders: A meta-analysis. Complement Ther Clin Pract. 2023 Feb;50:101702. doi: 10.1016/j.ctcp.2022.101702. Epub 2022 Nov 8.

    PubMed 36423358
  • Song J, Liu ZZ, Huang J, Wu JS, Tao J. Effects of aerobic exercise, traditional Chinese exercises, and meditation on depressive symptoms of college student: A meta-analysis of randomized controlled trials. Medicine (Baltimore). 2021 Jan 8;100(1):e23819. doi: 10.1097/MD.0000000000023819.

    PubMed 33429742
  • Rodrigues, D. F., Rosa, F. T., Lima, R. A., Oliveira, M. C., & Oliveira, D. V. (2021). Assessment of Qigong effects on anxiety of high school students: A randomized controlled trial. Complementary Therapies in Clinical Practice, 43, 101348. https://doi.org/10.1016/j.ctcp.2021.101348

  • Wang X, Wu J, Ye M, Wang L, Zheng G. Effect of Baduanjin exercise on the cognitive function of middle-aged and older adults: A systematic review and meta-analysis. Complement Ther Med. 2021 Jun;59:102727. doi: 10.1016/j.ctim.2021.102727. Epub 2021 Apr 30.

    PubMed 33933577
  • Liu X, Li R, Cui J, Liu F, Smith L, Chen X, Zhang D. The Effects of Tai Chi and Qigong Exercise on Psychological Status in Adolescents: A Systematic Review and Meta-Analysis. Front Psychol. 2021 Nov 24;12:746975. doi: 10.3389/fpsyg.2021.746975. eCollection 2021.

    PubMed 34899487

Questions about this trial

What is this clinical trial studying?

A study testing Baduanjin Qigong and Passive Rest in people with University Students, run by Medipol University.

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 3 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: opening soon, as of the sponsor's last update on 17 Sep 2025. Status can change between updates, so confirm with the study contact before making plans.

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 HÜLYA YAMAN, Master's degree (+905419775047, ergoterapisthulya@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

State Anxiety (STAI-Y1) (time frame: Both at the start and end of all interventions within one hour). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT07178275, which also lists 7 linked publications.

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 17 Sep 2025.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in