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Efficacy and feasibility of the minimal therapist-guided four-week online audio-based mindfulness program Mindful Senses for burnout and stress reduction in medical personnel: A randomized controlled trial

Efficacy and feasibility of the minimal therapist-guided four-week online audio-based mindfulness program Mindful Senses for burnout and stress reduction in medical personnel: A randomized controlled trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
TCTR
Registry ID
TCTR20210416001
Enrollment
90
Registered
2021-04-16
Start date
2021-06-01
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Stress Burnout Depression Anxiety Mindfulness Quality of life Online Mindfulness Burnout Stress Medical personnel

Interventions

Group A read four weekly Psychological Self-Help Articles (PSA) and attended the MS program during weeks 1-4. ,Group B read PSA during weeks 1-4 and attended MS program during week 9-12.
Experimental Other,Experimental Other
Group A (MS + PSA),Group B (MS after PSA)

Sponsors

Routine to research unit Siriraj hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. physicians, dentists, pharmacists, nurses, practical nurses, medical technologists, physical therapists, traditional medical practitioners, or public health professionals aged 18 years or older 2. could use the LINE application 3. be able to communicate in Thai 4. have a Stress Test Questionnaire (ST-5) score greater than or equal to 5, and a Thai version of the Copenhagen Burnout Inventory (T-CBI) score greater than or equal to 50.

Exclusion criteria

Exclusion criteria: 1. had practiced mindfulness at least five days per week for more than one year 2. was receiving psychotherapy 3. started treatment for psychiatric illness during the last three months 4. started taking a new psychotropic medication during the last three months 5. had any taking psychotropic medication dose adjusted during the last three months.

Design outcomes

Primary

MeasureTime frame
Burnout level Weeks 0, 4, 8 (Group A), Weeks 0, 4, 8, 12, 16 (Group B) self reported questionnaire: T-CBI,Stress level Weeks 0, 4, 8 (Group A), Weeks 0, 4, 8, 12, 16 (Group B) self reported questionnaire: ST-5—

Secondary

MeasureTime frame
Mindfulness level Weeks 0, 4, 8 (Group A), Weeks 0, 4, 8, 12, 16 (Group B) self reported questionnaire: TH PHLMS,Depression and anxiety level Weeks 0, 4, 8 (Group A), Weeks 0, 4, 8, 12, 16 (Group B) self reported questionnaire: Thai HADS,Quality of life Weeks 0, 4, 8 (Group A), Weeks 0, 4, 8, 12, 16 (Group B) self reported questionnaire: WHOQOL-BREF-THAI—

Countries

Thailand

Contacts

Public ContactNatee Viravan

Department of Psychiatry, Siriraj hospital, Mahidol university

natee.vir@mahidol.ac.th0814832284

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026