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Feasibility and Acceptability Study of Pulihkan Luka: a website-based psychoeducational program for trauma-related symptoms

Feasibility and Acceptability Study of Pulihkan Luka: a website-based psychoeducational program for trauma-related symptoms in an Indonesian undergraduate student population

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
TCTR
Registry ID
TCTR20230721001
Enrollment
130
Registered
2023-07-21
Start date
2023-11-21
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

Help-seeking intention for mental health complaints, psychological well-being, mental health literacy, and symptoms of PTSD, depression, anxiety, and insomnia in Indonesian undergraduate students population with trauma-related experience and probable trauma-related mental health disorders. Help-Seeking Behavior, Psychological Well Being, Post-Traumatic Stress Disorder, Depression, Anxiety, Insomnia,

Interventions

The Pulihkan Luka (PL) Program involves four to seven 30-minute website-based personalized psychoeducation modules that enhance participants understanding of how trauma exposure can affect physical an
Experimental Behavioral,No Intervention Other
Pulihkan Luka (PL) Program,Enhanced Usual Care (EUC)

Sponsors

Center of Psychological Trauma
Lead Sponsor
Amsterdam Public Health (APH) Global Health Program
Collaborator

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Enrollment as an undergraduate student living in Indonesia 2. Having experienced at least one traumatic event according to the Life Event Checklist for DSM-5 (LEC-5) 3. Endorsing items of the Global Psychotrauma Screen (GPS) indicating at least one probable mental disorder related to the traumatic event (PTSD, Complex PTSD, anxiety, depression, insomnia, and self-harm) 4. Proficient in the Indonesian language 5. Having access to internet broadband

Exclusion criteria

Exclusion criteria: Currently receiving psychological or medical treatment (counseling/psychotherapy/psychotropic medications) for mental health problems.

Design outcomes

Primary

MeasureTime frame
Feasibility (intervention uptake, intervention adherence, and feasibility) One week after the intervention phase (post-intervention asessment/T2) percentage of module attendance, MT4C-in Care feasibility survey score,Acceptability (Intention to use the PL Program, and User satisfaction) One week after the intervention phase (post-intervention asessment/T2) Internet-based Interventions Acceptability Questionnaire-Indonesia (IIAQ-ID) score, SIN-E-Stress user satisfaction survey score

Secondary

MeasureTime frame
Help-seeking intention Baseline (T1), 1 week after the intervention phase (post-intervention asessment/T2), approximately 90 days and 180 days after the intervention phase (3-month and 6-month follow-up assessment/T3 & T4) The General Help-Seeking Questionnaire (GHSQ) score,Psychological Well-being Baseline (T1), 1 week after the intervention phase (post-intervention asessment/T2), approximately 90 days and 180 days after the intervention phase (3-month and 6-month follow-up assessment/T3 & T4) The World Health Organization-Five Well Being Index (WHO-5) score ,PTSD symptoms Baseline (T1), 1 week after the intervention phase (post-intervention asessment/T2), approximately 90 days and 180 days after the intervention phase (3-month and 6-month follow-up assessment/T3 & T4) The PTSD Checklist for DSM-5 (PCL-5) score,Depression symptoms Baseline (T1), 1 week after the intervention phase (post-intervention asessment/T2), approximately 90 days and 180 days after the intervention phase (3-month and 6-month follow-up assessment/T3 & T4) The Patient Health Questionnaire (PHQ-9) score,Anxiety symptoms Baseline (T1), 1 week after the intervention phase (post-intervention asessment/T2), approximately 90 days and 180 days after the intervention phase (3-month and 6-month follow-up assessment/T3 & T4) The General Anxiety Disorder (GAD-7) score,Insomnia symptoms Baseline (T1), 1 week after the intervention phase (post-intervention asessment/T2), approximately 90 days and 180 days after the intervention phase (3-month and 6-month follow-up assessment/T3 & T4) The Insomnia Severity Index (ISI) score,Mental health literacy Baseline (T1), 1 week after the intervention phase (post-intervention asessment/T2), approximately 90 days and 180 days after the intervention phase (3-month and 6-month follow-up assessment/T3 & T4) Mental health literacy questionnaire score

Countries

Netherlands

Contacts

Public ContactIndira Primasari

Amsterdam UMC

i.d.primasari@amsterdamumc.nl3120 891360

Outcome results

None listed

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