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Effects of Mindfulness Training on Emotional Care

The University of Hong Kong (HKU) logo

The University of Hong Kong (HKU)

Status

Completed

Conditions

Mental Health Issue

Treatments

Behavioral: 8-week mindfulness program

Study type

Interventional

Funder types

Other

Identifiers

NCT04518631
UHongKong(PandA)

Details and patient eligibility

About

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 investigate 1) the effects of mindfulness training on teachers' well-being (i.e. general health, positive affect, life satisfaction, stress, negative affect), and 2) the mechanisms underlying the effectiveness of mindfulness (i.e. emotional care strategies including anchoring, decentering, and acceptance). Participants will be randomized to either intervention (8-week .b Foundations/ .begin course) or waiting-list control condition. They will complete survey before (baseline), after (post-intervention), and two-months (follow-up) after the intervention.

Enrollment

299 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

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

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

299 participants in 2 patient groups

8-week mindfulness program
Experimental group
Description:
8-week .b Foundations course
Treatment:
Behavioral: 8-week mindfulness program
Wait-list control
No Intervention group
Description:
Participants in wait-list control group will receive the same intervention, two months after their counterparts in experimental group completed the intervention.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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