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Mindfulness, Compassion and Self-compassion

Mindfulness, Compassion and Self-compassion

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05046691
Enrollment
328
Registered
2021-09-16
Start date
2021-10-01
Completion date
2022-04-30
Last updated
2022-05-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Mental Health Issue

Keywords

mindfulness, teacher mental health, compassion, self-compassion, common humanity, mindfulness-based intervention for teachers

Brief summary

Teachers in Hong Kong are susceptible to professional stress and its associated psychosomatic illnesses. To enhance teachers' well-being, mindfulness training is conducted in local schools. The present study is a randomized controlled trial to explore 1) the relationship between mindfulness, common humanity, self-compassion, compassion, and well-being of school teachers; 2) whether mindfulness and common humanity are the antecedents of self-compassion and compassion; 3) the conditions under which compassion and self-compassion are highly correlated. Participants will be randomized to either intervention (8-week .b Foundations course) or waiting-list control condition. They will complete an online survey before (baseline), after (post-intervention), and two-months (follow-up) after the intervention.

Interventions

The .b Foundations course is an 8-week mindfulness program developed by Mindfulness in Schools Project (MiSP) for school teachers and personnel. It includes a taster session and 8 weekly sessions. Each session lasts for 1.5 hours with a specific theme (e.g. Lesson 1 waking up from autopilot). Formal and informal mindfulness practices (e.g. mindful eating, body scan, mindful walking, habit releaser etc.), psychoeducation, cognitive exercises, inquiry, and home practice are involved.

Sponsors

The University of Hong Kong
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Aged 18 years old or above * Working in local schools or education institutions * Willing to participate in mindfulness training voluntarily

Exclusion criteria

* Experiencing severe or unstable mental health condition currently * Completed 8-week mindfulness training previously * Unwilling to go by random assignment

Design outcomes

Primary

MeasureTime frameDescription
Change in General HealthBaseline, Immediately after intervention, Two-months after interventionGeneral Health Questionnaire (GHQ), 12 items, 5-point Likert scale ranging from 1 (never) to 5 (always)
Change in StressBaseline, Immediately after intervention, Two-months after interventionPerceived Stress Scale (PSS), 10 items, 5-point Likert scale ranging from 1 (never) to 5 (always)

Secondary

MeasureTime frameDescription
Change in CompassionBaseline, Immediately after intervention, Two-months after interventionCompassion scale, 6 items, 5-point Likert scale ranging from 1 (never) to 5 (always)
Change in Self-compassionBaseline, Immediately after intervention, Two-months after interventionSelf-compassion scale, 6 items, 5-point Likert scale ranging from 1 (never) to 5 (always)
Change in Positive affectBaseline, Immediately after intervention, Two-months after interventionPositive and Negative Affect Schedule (PANAS), 4 items, 5-point Likert scale ranging from 1 (never) to 5 (always)
Change in MindfulnessBaseline, Immediately after intervention, Two-months after interventionCognitive and Affective Mindfulness Scale-Revised (CAMS-R), 12 items, 5-point Likert scale ranging from 1 (never) to 5 (always)
Change in Common humanityBaseline, Immediately after intervention, Two-months after interventionCommon Humanity scale, 10 items, 5-point Likert scale ranging from 1 (never) to 5 (always)
Change in Negative affectBaseline, Immediately after intervention, Two-months after interventionPositive and Negative Affect Schedule (PANAS), 4 items, 5-point Likert scale ranging from 1 (never) to 5 (always)

Countries

Hong Kong

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026