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Mental Health IssueNCT05046691

Mindfulness, Compassion and Self-compassion

A study testing 8-week mindfulness program in people with Mental Health Issue, run by The University of Hong Kong at 1 site in Hong Kong.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial 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. Read more about this study

Who is it for?
Ages 18 years and olderHealthy volunteers can take part
Conditions the study is for
Mental Health Issue
What is being tested?
8-week mindfulness program
Could I receive a placebo?
No, everyone receives an active treatment
How many people
328 participants
Where
1 siteHong Kong
Study dates
1 Oct 2021to 30 Apr 2022
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

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

Who cannot join

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

Trial locations and contacts

1 site in 1 country.

Hong Kong1 site
  • Jockey Club "Peace and Awareness" Mindfulness Culture in Schools Initiative, Faculty of Social Sciences, The University of Hong Kong

    Hong Kong

Other trials in Hong Kong

About this study

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.

Being tested
8-week mindfulness program
Keywords
mindfulness, teacher mental health, compassion, self-compassion, common humanity, mindfulness-based intervention for teachers

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • 8-week mindfulness programBehavioural

    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.

Study groups in NCT05046691
Study groupRoleWhat they receive
Intervention groupExperimental8-week .b Foundations course
Receives: Behavioral: 8-week mindfulness program
Wait-list controlNo interventionParticipants in wait-list control group will receive the same intervention, two months after their counterparts in experimental group completed the intervention.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Change in General Health

    General Health Questionnaire (GHQ), 12 items, 5-point Likert scale ranging from 1 (never) to 5 (always)

    Measured: Baseline, Immediately after intervention, Two-months after intervention

  2. Change in Stress

    Perceived Stress Scale (PSS), 10 items, 5-point Likert scale ranging from 1 (never) to 5 (always)

    Measured: Baseline, Immediately after intervention, Two-months after intervention

Secondary outcomes (6)
  1. Change in Positive affect

    Positive and Negative Affect Schedule (PANAS), 4 items, 5-point Likert scale ranging from 1 (never) to 5 (always)

    Measured: Baseline, Immediately after intervention, Two-months after intervention

  2. Change in Negative affect

    Positive and Negative Affect Schedule (PANAS), 4 items, 5-point Likert scale ranging from 1 (never) to 5 (always)

    Measured: Baseline, Immediately after intervention, Two-months after intervention

  3. Change in Compassion

    Compassion scale, 6 items, 5-point Likert scale ranging from 1 (never) to 5 (always)

    Measured: Baseline, Immediately after intervention, Two-months after intervention

  4. Change in Self-compassion

    Self-compassion scale, 6 items, 5-point Likert scale ranging from 1 (never) to 5 (always)

    Measured: Baseline, Immediately after intervention, Two-months after intervention

  5. Change in Common humanity

    Common Humanity scale, 10 items, 5-point Likert scale ranging from 1 (never) to 5 (always)

    Measured: Baseline, Immediately after intervention, Two-months after intervention

  6. Change in Mindfulness

    Cognitive and Affective Mindfulness Scale-Revised (CAMS-R), 12 items, 5-point Likert scale ranging from 1 (never) to 5 (always)

    Measured: Baseline, Immediately after intervention, Two-months after intervention

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted16 Sep 2021
  2. Study start1 Oct 2021
  3. Primary completion30 Apr 2022
  4. Study completion30 Apr 2022

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Prevention
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Participant
Enrolment
328 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05046691
Sponsor's protocol ID
UHongKong (PandA)
Status last verified
May 2022
First submitted
8 Sep 2021
Last updated
18 May 2022
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing 8-week mindfulness program in people with Mental Health Issue, run by The University of Hong Kong at 1 site in Hong Kong.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 18 May 2022. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Hong Kong. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Change in General Health (time frame: Baseline, Immediately after intervention, Two-months after intervention). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 18 May 2022.

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Mindfulness, Compassion and Self-compassion | AzTrials