- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06926361
Effects of Mindfulness-based Interventions on Improving Teacher Wellbeing and Teaching Outcomes: A Multi-site, Mixed-methods Randomized Controlled Study
March 17, 2026 updated by: Jennifer Yee Man Tang, Chinese University of Hong Kong
Effects of Mindfulness-based Interventions on Improving Teacher Wellbeing and Teaching Outcomes
This study aims to evaluate the effectiveness of MBCT-L among Chinese teachers on their mental well-being and teaching outcomes and explore the mechanisms of how mindfulness practice brings these benefits.
The study is a multi-site, mixed-methods randomized controlled trial including 160 teachers.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Estimated)
160
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Jennifer Tang, PhD
- Phone Number: 852-39435677
- Email: jymtang@cuhk.edu.hk
Study Locations
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-
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Hong Kong, Hong Kong
- Recruiting
- The Chinese University of Hong Kong
-
Contact:
- Jennifer YM Tang
- Phone Number: +852-3943-6904
- Email: jymtang@cuhk.edu.hk
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-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Teachers aged 21-65 years;
- Teachers currently working in a school; and
- Teachers willing to commit time for the 8-week course.
Exclusion Criteria:
- Teachers previously joined a related group mindfulness-based intervention, such as mindfulness-based cognitive therapy (MBCT), mindfulness-based stress reduction (MBSR), Mindfulness - Finding Peace in a Frantic World (FPFW); or
- Teachers who are mentally unstable or having active suicidal risk.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Mindfulness for Life
MBCT-L is an 8-week program consisting of mindfulness practices and cognitive-behavioral techniques with 8 sessions (2 hours and 15 minutes per session) and one-day retreat that can provide participants with an extended period to deepen their personal mindfulness practices.
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Behavioral: Mindfulness for Life (MBCT-L) MBCT-L is an 8-week program consisting of mindfulness practices and cognitive-behavioral techniques with 8 sessions (2 hours and 15 minutes per session) and one-day retreat that can provide participants with an extended period to deepen their personal mindfulness practices.
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Active Comparator: Positive education training
Positive Education program is an 8-week course consisting of theories and activities of positive psychology to enhance teachers' skills to support students' learning and wellbeing using a strength-based approach.
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Positive Education program is an 8-week course consisting of theories and activities of positive psychology to enhance teachers' skills to support students' learning and wellbeing using a strength-based approach.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Teaching efficacy
Time Frame: Baseline, 9 weeks, and 3 months post-intervention
|
The Teachers' Sense of Efficacy Scale-Short Form (TSES-SF).
Participants will rate their responses on a 9-point Likert scale ranging from 1 (nothing) to 9 (a great deal).
A higher total score indicates a higher sense of teaching efficacy of teachers.
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Baseline, 9 weeks, and 3 months post-intervention
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Teaching practices
Time Frame: Baseline, 9 weeks, and 3 months post-intervention
|
The Classroom Strategies Scale-Teacher Form (CSS-T).
Participants will rate their frequency of using a specific strategy in two domains on a 7-point Likert scale from 1 (never used) to 7 (always used).
Higher scores indicate teachers use specific strategies more frequently.
|
Baseline, 9 weeks, and 3 months post-intervention
|
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Classroom climate
Time Frame: Baseline, 9 weeks, and 3 months post-intervention
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Three subscales of Delaware School Climate Scale-Teacher/Staff (DSCS-T/S): Student-Student Relations, Student Engagement, and Clarity of Expectations.
It uses a 4-point Likert scale from 1 (disagree a lot) to 4 (agree a lot).
A higher total score indicates a better classroom climate.
|
Baseline, 9 weeks, and 3 months post-intervention
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Stress
Time Frame: Baseline, 9 weeks, and 3 months post-intervention
|
The Perceived Stress Scale.
Participates rate their stress on a 5-point Likert scale ranging from 0 (never) to 4 (very often).
A higher total score indicates higher stress levels.
|
Baseline, 9 weeks, and 3 months post-intervention
|
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Anxiety
Time Frame: Baseline, 9 weeks, and 3 months post-intervention
|
Generalized Anxiety Disorder Assessment (GAD-7).
The items are rated on a 4-point Likert scale ranging from 0 (not at all) to 3 (nearly every day) over the past two weeks.
A higher total score indicates a higher level of anxiety.
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Baseline, 9 weeks, and 3 months post-intervention
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Depression
Time Frame: Baseline, 9 weeks, and 3 months post-intervention
|
The Patient Health Questionnaire-9 (PHQ-9).
The items are rated on a 4-point Likert scale ranging from 0 (not at all) to 3 (nearly every day) over the past two weeks.
A higher total score indicates higher depressive symptoms.
|
Baseline, 9 weeks, and 3 months post-intervention
|
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Burnout
Time Frame: Baseline, 9 weeks, and 3 months post-intervention
|
Maslach Burnout Inventory - Educators Survey (MBI-ES).
Participants report scores on a 7-point Likert scale ranging from 0 (never) to 6 (every day).
A higher total score indicates a higher level of burnout.
|
Baseline, 9 weeks, and 3 months post-intervention
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Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Trait mindfulness
Time Frame: Baseline, 9 weeks, and 3 months post-intervention
|
The Five-Facet Mindfulness Questionnaire (FFMQ-15).
Participants give ratings on a 5-point Likert scale from 1 (never or very rarely true) to 5 (very often or always true).
A higher total score means a higher level of trait mindfulness.
|
Baseline, 9 weeks, and 3 months post-intervention
|
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Emotion regulation
Time Frame: Baseline, 9 weeks, and 3 months post-intervention
|
The Emotion Regulation Questionnaire (ERQ).
Participants will rate their responses on a 7-point Likert scale ranging from 1 (strongly disagree) to 7 (strongly agree).
A higher total score in each subscale indicates a higher tendency of using the specific emotion regulation strategy.
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Baseline, 9 weeks, and 3 months post-intervention
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
May 15, 2025
Primary Completion (Estimated)
June 30, 2027
Study Completion (Estimated)
December 31, 2027
Study Registration Dates
First Submitted
April 7, 2025
First Submitted That Met QC Criteria
April 7, 2025
First Posted (Actual)
April 13, 2025
Study Record Updates
Last Update Posted (Actual)
March 19, 2026
Last Update Submitted That Met QC Criteria
March 17, 2026
Last Verified
March 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- SBRE-24-0445
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
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