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CompletedNCT07741422Updated Aug 3, 2026

Investigating a Mediation Model of Emotion Regulation and Psychological Resilience in Relationship Between Mindfulness and Negative Emotions Among College Students in Guangzhou

An interventional study of Mindfulness-Based Intervention and Health Education in Depression, Anxiety and Stress, sponsored by Universiti Sains Malaysia. Completed at 1 site in China. Open to participants aged 18 Years to 30 Years. Per ClinicalTrials.gov, last updated 2026-08-03.

Sponsored by Universiti Sains Malaysia · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 3 months after the study started (first participant enrolled Apr 2026, registered Jul 2026).
Phase
Not applicable
Study type
Interventional
Enrollment
135
Allocation
Randomized
Ages
18 Years to 30 Years
Sex
All
01

Study summary

This study examines whether a four-week mindfulness-based intervention can reduce depression, anxiety, and stress among college students in Guangzhou, China. It also investigates whether changes in mindfulness, emotion regulation, and psychological resilience may help explain the effects of the intervention.

Eligible participants will be randomly assigned to either a mindfulness intervention group or a health education control group. The intervention group will receive weekly mindfulness-based training and complete brief daily mindfulness practice, while the control group will receive health education sessions. Participants will complete questionnaires assessing mindfulness, cognitive reappraisal, expressive suppression, psychological resilience, depression, anxiety, and stress before and after the intervention and at follow-up.

02

Conditions studied

  • Depression
  • Anxiety
  • Stress

Keywords

  • Mindfulness
  • Mindfulness-Based Intervention
  • Emotion Regulation
  • Cognitive Reappraisal
  • Expressive Suppression
  • Psychological Resilience
  • College Students
  • Negative Emotions
03

In context

Depression

8,057 studies on the registry are indexed under Depression; 1,641 are open to participants now.

This study's enrollment of 135 is above the median of 84 across 6,720 interventional studies indexed under Depression.

Browse Depression studies →

Lead sponsor

Universiti Sains Malaysia is the lead sponsor of 171 studies on the registry; 48 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 30 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • - Full-time college students enrolled at a participating institution in Guangzhou, China.
  • Aged 18 to 30 years.
  • Able to read and understand Chinese.
  • Willing to provide informed consent.
  • Completed the initial questionnaire assessment.
  • Reported at least mild symptoms of depression, anxiety, or stress on at least one subscale of the Depression Anxiety Stress Scales-21.
  • Willing and able to participate in the four-week intervention and complete the required assessm

Exclusion criteria

Exclusion Criteria:

  • - Currently receiving psychiatric or psychological treatment.
  • Diagnosed with a severe mental disorder or other severe psychopathology that could interfere with participation.
  • At acute risk of suicide or self-harm.
  • Currently participating in another psychological or mental health intervention.
  • Currently engaging in regular mindfulness meditation or enrolled in another mindfulness-based program.
  • Pregnant.
  • Having a physical or medical condition that prevents participation in the intervention activities.
  • Unable to complete the intervention or study assessments.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
135 participants (actual)

Study arms

  • Experimental
    Mindfulness-Based Intervention

    Participants in this arm will receive a four-week mindfulness-based intervention. The program includes weekly group sessions and brief daily home practice focusing on mindful breathing, body awareness, mindful movement, and awareness of thoughts and emotions.

    Behavioral: Mindfulness-Based Intervention

  • Active comparator
    Health Education Control Group

    Participants in this arm will receive health education sessions of comparable frequency and duration, focusing on stress management, emotional well-being, and healthy lifestyle practices.

    Behavioral: Health Education

Interventions

  • BehavioralMindfulness-Based Intervention

    Participants received a four-week mindfulness-based intervention consisting of one 90-minute group session per week and approximately 10 minutes of daily home practice. The program included mindful breathing, body scan practice, mindful movement, awareness of thoughts and emotions, and exercises for responding to stress. The intervention was adapted from mindfulness-based stress reduction principles for college students.

  • BehavioralHealth Education

    Participants received a four-week health education program consisting of one group session per week. The sessions addressed general stress management, emotional well-being, healthy lifestyle practices, and other health-related topics. The program did not include mindfulness meditation or formal mindfulness practice.

06

What researchers measure

Primary outcomes

  1. Change in Depression, Anxiety, and Stress Symptoms Assessed by the Depression Anxiety Stress Scales-21

    Depression, anxiety, and stress symptoms will be assessed using the 21-item Depression Anxiety Stress Scales (DASS-21). The scale contains three 7-item subscales measuring depression, anxiety, and stress. Each item is rated from 0 to 3. Subscale scores are summed and multiplied by two, with higher scores indicating greater symptom severity.

    Time frame: Baseline and immediately after the 4-week intervention

Secondary outcomes

  1. Change in Mindfulness Assessed by the 15-Item Five Facet Mindfulness Questionnaire

    Mindfulness will be assessed using the 15-item Five Facet Mindfulness Questionnaire (FFMQ-15). Items are rated on a Likert-type scale and summed to produce a total score, with higher scores indicating a higher level of mindfulness.

    Time frame: Baseline and immediately after the 4-week intervention

  2. Change in Cognitive Reappraisal Assessed by the Emotion Regulation Questionnaire

    Cognitive reappraisal will be assessed using the 6-item cognitive reappraisal subscale of the Emotion Regulation Questionnaire. Items are rated from 1 to 7 and summed, with higher scores indicating greater use of cognitive reappraisal.

    Time frame: Baseline and immediately after the 4-week intervention

  3. Change in Expressive Suppression Assessed by the Emotion Regulation Questionnaire

    Expressive suppression will be assessed using the 4-item expressive suppression subscale of the Emotion Regulation Questionnaire. Items are rated from 1 to 7 and summed, with higher scores indicating greater use of expressive suppression.

    Time frame: Baseline and immediately after the 4-week intervention

  4. Change in Psychological Resilience Assessed by the Connor-Davidson Resilience Scale

    Psychological resilience will be assessed using the Connor-Davidson Resilience Scale. Item scores are summed to produce a total score, with higher scores indicating greater psychological resilience.

    Time frame: Baseline and immediately after the 4-week intervention

07

Study locations

1 site
  • Guangzhou City Construction College
    Guangzhou, Guangdong 715517, China
08

References and documents

Individual participant data

Plan to share: No — Individual participant data will not be shared publicly because the consent obtained from participants did not specifically include public or external sharing of individual-level data. Only aggregated and de-identified study findings will be reported in publications and academic presentations.

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 3, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07741422
Lead sponsor
Universiti Sains Malaysia
Responsible party
Wang Donglin (PHD, Universiti Sains Malaysia) — Principal investigator
First posted
Aug 3, 2026
Start date
Apr 1, 2026
Primary completion
Apr 20, 2026
Completion
May 20, 2026
Last update
Aug 3, 2026

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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