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A brief mindfulness intervention based on mobile apps to reduce anxiety and stress for Indonesian senior high school teachers: A Pilot Randomized Controlled Trial

A brief mindfulness intervention based on mobile apps to reduce anxiety and stress for Indonesian senior high school teachers: A Pilot Randomized Controlled Trial - BM-MA

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300068085
Enrollment
Unknown
Registered
2023-02-06
Start date
2023-02-01
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

Mental health

Interventions

Intervention group:Mindfulness-based app
Control group:None

Sponsors

Universitas Pendidikan Ganesha, Indonesia
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Indonesian-certified senior high school teachers who are able to read and write in Indonesian; 2. Adults who are above 18 years of age; 3. Have access to smartphone use; 4. The total GAD-7 score is no more than 14 and the total GHQ-12 score is no more than 20.

Exclusion criteria

Exclusion criteria: The exclusion criteria for randomized controlled trial are set based on guidelines from MBSR (Santorelli, 2014) and MBCT (Crane et al., 2012), and include 1. Engagement with regular practice of mindfulness meditation [e.g for 15-20 mins a day, 2-3 times a week; 2. A history of, presence, or ongoing treatment for a psychological disorder; 3. A positive answer to GHQ-12 questions regarding suicidal; 4. Refusal to fill in the informed consent.

Design outcomes

Primary

MeasureTime frame
Feasibility;Anxiety;Somatic and social dysfunction;—

Secondary

MeasureTime frame
Life satisfaction;Teacher sense self-efficacy;Self-compassion;—

Countries

Indonesia

Contacts

Public ContactDr. Ni Komang Arie Suwastini

Universitas Pendidikan Ganesha, Indonesia

arie.suwastini@undiksha.ac.id+62 819 3310 0024

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 5, 2026