Investigating a Mediation Model of Emotion Regulation and Psychological Resilience in Relationship Between Mindfulness and Negative Emotions Among College Students in Guangzhou
1 other identifier
interventional
135
1 country
1
Brief 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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable depression
Started Apr 2026
Shorter than P25 for not_applicable depression
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
April 1, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 20, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
May 20, 2026
CompletedFirst Submitted
Initial submission to the registry
July 27, 2026
CompletedFirst Posted
Study publicly available on registry
August 3, 2026
CompletedAugust 3, 2026
January 1, 2026
19 days
July 27, 2026
July 29, 2026
Conditions
Keywords
Outcome Measures
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.
Baseline and immediately after the 4-week intervention
Secondary Outcomes (4)
Change in Mindfulness Assessed by the 15-Item Five Facet Mindfulness Questionnaire
Baseline and immediately after the 4-week intervention
Change in Cognitive Reappraisal Assessed by the Emotion Regulation Questionnaire
Baseline and immediately after the 4-week intervention
Change in Expressive Suppression Assessed by the Emotion Regulation Questionnaire
Baseline and immediately after the 4-week intervention
Change in Psychological Resilience Assessed by the Connor-Davidson Resilience Scale
Baseline and immediately after the 4-week intervention
Study Arms (2)
Mindfulness-Based Intervention
EXPERIMENTALParticipants 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.
Health Education Control Group
ACTIVE COMPARATORParticipants in this arm will receive health education sessions of comparable frequency and duration, focusing on stress management, emotional well-being, and healthy lifestyle practices.
Interventions
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.
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.
Eligibility Criteria
You may qualify if:
- \- 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
You may not qualify if:
- \- 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.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Guangzhou City Construction College
Guangzhou, Guangdong, 715517, China
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- PHD
Study Record Dates
First Submitted
July 27, 2026
First Posted
August 3, 2026
Study Start
April 1, 2026
Primary Completion
April 20, 2026
Study Completion
May 20, 2026
Last Updated
August 3, 2026
Record last verified: 2026-01
Data Sharing
- IPD Sharing
- Will not share
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.