NCT06125379

Brief Summary

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

Trial Health

55
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
80

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Oct 2023

Geographic Reach
1 country

1 active site

Status
active not recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

September 26, 2023

Completed
19 days until next milestone

Study Start

First participant enrolled

October 15, 2023

Completed
25 days until next milestone

First Posted

Study publicly available on registry

November 9, 2023

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 25, 2024

Completed
1.2 years until next milestone

Study Completion

Last participant's last visit for all outcomes

June 25, 2025

Completed
Last Updated

May 22, 2025

Status Verified

May 1, 2025

Enrollment Period

6 months

First QC Date

September 26, 2023

Last Update Submit

May 18, 2025

Conditions

Keywords

mindfulnessteacherIndonesiaperceived stresswell-being

Outcome Measures

Primary Outcomes (1)

  • Perceived Stress Scale (PSS

    The Perceived Stress Scale (PSS-10) is a 10-item questionnaire widely used to assess stress levels in young people and adults aged 12 and above. It evaluates the degree to which an individual has perceived life as unpredictable, uncontrollable and overloading over the previous month. The PSS score is obtained by summing across all items. A total PSS-10 score from 0 to 40 is presented, with higher scores representing higher levels of stress.

    4 weeks

Secondary Outcomes (2)

  • Indonesian Well-being Scale (IWS)

    4 weeks

  • Five Facet Mindfulness Scale (FFMQ)

    4 weeks

Study Arms (2)

MindCARE

EXPERIMENTAL

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.

Behavioral: brief mindfulness

Wait-list control group

NO INTERVENTION

Group B is the wait-list control group which did not receive any intervention for 4 weeks.

Interventions

The mindfulness intervention protocol in this study is an adaptation of the Mindfulness Based Stress Reduction (MBSR) protocol with the cultural adaptation suits Indonesia population with addition of Islamic elements (i.e., a series of spiritual approaches) to improve emotional regulation, make sense of their life, be grateful and feel closer to God.

Also known as: MindCARE (Mindfulness for Compassion and Relieve Stress)
MindCARE

Eligibility Criteria

Age25 Years - 55 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • 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

You may not qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Ahmad Dahlan University

Yogyakarta, 55166, Indonesia

Location

MeSH Terms

Conditions

Stress, Psychological

Interventions

Mindfulness

Condition Hierarchy (Ancestors)

Behavioral SymptomsBehavior

Intervention Hierarchy (Ancestors)

Cognitive Behavioral TherapyBehavior TherapyPsychotherapyBehavioral Disciplines and Activities

Study Officials

  • Jamilah HA Khaiyom, Doctoral

    International Islamic University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

September 26, 2023

First Posted

November 9, 2023

Study Start

October 15, 2023

Primary Completion

April 25, 2024

Study Completion

June 25, 2025

Last Updated

May 22, 2025

Record last verified: 2025-05

Data Sharing

IPD Sharing
Will not share

Locations