ClinicalTrials.Veeva

Menu

Brief Mindfulness-based Intervention for Indonesian Teacher in Rural Area

I

International Islamic University Malaysia

Status

Active, not recruiting

Conditions

Stress, Psychological

Treatments

Behavioral: brief mindfulness

Study type

Interventional

Funder types

Other

Identifiers

NCT06125379
012211183

Details and patient eligibility

About

A randomized controlled trial to assess the effectiveness of the brief mindfulness on teachers' perceived stress and their psychological well-being.

Full description

Teacher in early childhood education (ECE) in Indonesia is experiencing high intense stress due to work environment, class management, child behaviour problem, and lack administrative support. Stress has also shown negatively impact their psychological well-being, quality of teaching, and to children's' executive function. Research about stress and the effects on teacher well-being is especially lacking for rural schools. They represent a forgotten minority and thus, teacher from rural area need a prompt and direct support in terms of stress management strategies.

This study employs a randomized wait-list controlled trial design (RCT) with an assessment before and after treatment. 4-weeks brief mindfulness-based protocol will be given to 40 teachers as experimental group. 40 other teachers receive wait-list treatment will assign as control group. Measurement of perceived stress level will be using Indonesian version of Perceived Stress Scale (PSS), psychological wellbeing will be measure using Indonesian Well-being Scale (IWS), and mindfulness traits will be measure using Indonesian version of Five Factor Mindfulness Questionnaire (FFMQ). Data analysis using MANOVA and ANOVA to measure the differences between groups and within groups for all tests and constructs measured.

Enrollment

80 patients

Sex

All

Ages

25 to 55 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • minimum two years of work experience as early childhood education teacher.
  • minimum 25 years of age.
  • scoring Moderate (total score 14-26) to High (total score 27-40) perceived stress on PSS-10

Exclusion criteria

  • have received any formal / manualized mindfulness training prior.
  • have ever been diagnosed with chronic stress or other related mental disorders such as anxiety, depression, PTSD.
  • people with a history or tendency to commit suicide.
  • people with addictive substance dependence who are recovering less than one year.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

80 participants in 2 patient groups

MindCARE
Experimental group
Description:
Group A is an experimental group that will receive mindfulness intervention for 4 consecutive weeks. Group A consists of 2-3 cohorts with 10-15 subjects per cohort.
Treatment:
Behavioral: brief mindfulness
Wait-list control group
No Intervention group
Description:
Group B is the wait-list control group which did not receive any intervention for 4 weeks.

Trial documents
2

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems