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CompletedNCT03614390Updated Feb 4, 2019

Mindfulness for Medical Students

An interventional study of mindfulness based cognitive therapy (MBCT) in Mindfulness and Burnout, Professional, sponsored by Chinese University of Hong Kong. Completed at 1 site in Hong Kong. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2019-02-04.

Sponsored by Chinese University of Hong Kong · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
24
Allocation
Not applicable
Ages
18 Years and older
Sex
All
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Study summary

Burnout is common among medical students. Previous studies had shown that mindfulness based interventions may improve burnout and quality of life in medical students. Mindfulness-based cognitive therapy (MBCT) is one of the most often used mindfulness based interventions.

Medical students in the Chinese University of Hong Kong are invited to a MBCT on voluntary basis. They will be asked to fill in questionnaire that measures burnout, depression/anxiety, quality of life, and mindfulness at beginning and end of the MBCT. The pre-group and post-group data will be compared and analysed

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Conditions studied

  • Mindfulness
  • Burnout, Professional

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03

In context

Burnout, Professional

214 studies on the registry are indexed under Burnout, Professional; 33 are open to participants now.

This study's enrollment of 24 is below the median of 80 across 158 interventional studies indexed under Burnout, Professional.

Browse Burnout, Professional studies →

Lead sponsor

Chinese University of Hong Kong is the lead sponsor of 1,419 studies on the registry; 487 are open to participants now.

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

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Medical students studying in Chinese University of Hong Kong

Exclusion criteria

Exclusion Criteria:

  • The investigators did not set any exclusion criteria
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Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
24 participants (actual)

Study arms

  • Other
    MBCT group

    There is only 1 arm in the study. The MBCT will be conducted according to the treatment manual. The program consists of eight weekly sessions. In between sessions, participants are advised to practice mindfulness meditations for 40-50 minutes every day. The teachers of the program will teach on voluntary basis. The teachers must have attended the 1-year foundation course to teach mindfulness (available in the United Kingdom and Hong Kong), regular mindfulness practice and must have at least yearly mindfulness retreat. This is in accordance to the good practice guidelines developed in the UK for mindfulness teachers

    Behavioral: mindfulness based cognitive therapy (MBCT)

Interventions

  • Behavioralmindfulness based cognitive therapy (MBCT)

    a well described and structured intervention, which is published previously. The psychoeducation materials in the MBCT will be titrated to discuss about low mood and burnout

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What researchers measure

Primary outcomes

  1. Maslach Burnout Inventory (MBI)

    The validated Maslach Burnout Inventory (MBI) is a 22-item questionnaire that assesses three aspects of professional burnout syndrome which includes emotional exhaustion, depersonalization and lack of personal accomplishment. It is widely used in research and has been widely used in studies about medical student well-being. In the scale, burnout is conceptualized as a continuous construct and participant is asked to rate their job related feelings using a 7-point Likert scale ranging from "never" to "everyday". A high degree of burnout is defined as a respondent who scores low on the Personal Accomplishment subscale but high in the Emotional Exhaustion and Depersonalization subscales of the instrument

    Time frame: 8 weeks (before and after MBCT; after 8 weekly sessions)

Secondary outcomes

  1. 21-item Depression Anxiety Stress Scale (DASS-21)

    The 21-item DASS-21 questionnaire will be used to assess the presence of depression, anxiety and tension/stress with 7 items per subscale. Each item is ranked from 0 (did not apply to me at all) to 3 (applied to me very much, or most of the time). The total score is computed by adding scores of each item and multiplying them by a factor of 2. Therefore, the total possible score ranges from 0 to 126. The questionnaire exhibits adequate validity and internal consistency among clinical and non-clinical samples

    Time frame: 8 weeks (before and after MBCT; after 8 weekly sessions)

  2. the World Health Organization Quality of Life Assessment (WHOQOL-BREF)

    The WHOQOL-BREF consisted of 26 items representing four underlying domains: environment, psychological, social relationship and physical health. Scores within each domain can be transformed to a scale of 0-100, with higher scores represent better quality of life. The scales was used in medical students' burnout research

    Time frame: 8 weeks (before and after MBCT; after 8 weekly sessions)

  3. Five Facet Mindfulness Questionnaire (FFMQ)

    The FFMQ consisted of 39 items representing five underlying constructs: observing, describing, acting with awareness, non-judging of inner experience and non-reactivity to inner experience. Each item is rated from 1 ("never or very rarely true) to 5 ("very often or always true"). Total Score can be obtained by summation of scores.The higher score represents a more mindful attitude in daily life.

    Time frame: 8 weeks (before and after MBCT; after 8 weekly sessions)

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Study locations

1 site
  • Lek Yuen Clinic
    Hong Kong, Hong Kong
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References and documents

Individual participant data

Plan to share: Undecided — Data will be made available on request from other researchers

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 4, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT03614390
Lead sponsor
Chinese University of Hong Kong
Responsible party
Lee Kam Pui (Clinical assistant professor, Chinese University of Hong Kong) — Principal investigator
First posted
Aug 3, 2018
Start date
Sep 7, 2018
Primary completion
Oct 26, 2018
Completion
Jan 28, 2019
Last update
Feb 4, 2019

Oversight

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

Not currently enrolling

This study is completed, as verified in Jan 2019. You cannot join it, but the record below documents what was studied.

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