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Culturally Adapted Psychological Support for Conflict-Affected Afghans: Study Protocol on Mental Health & Violence

No phase Interventional Depression and Suicide Ideation Anxiety PTSD

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Problem Management Plus with Emotional Processing module.
Who it may be relevant to
Registry conditions: Depression and Suicide Ideation, Anxiety, PTSD. Basic parameters: 16 years — 30 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Afghanistan
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Feasibility and Acceptability of Culturally Adapted, Evidence-Informed Psychological Support on Mental Health Symptoms and Violence for Conflict-Affected Populations in Afghanistan: A Study Protocol

Overview

This pilot study examines the feasibility and acceptability of a culturally adapted psychological intervention-Problem Management Plus with Emotional Processing (PM+ EP)-for young Afghans aged 16-30 experiencing high psychological distress. Through a pilot randomized control trial and qualitative interviews, the study explores whether PM+ EP can reduce symptoms of anxiety, depression, PTSD, and aggression, and improve daily functioning. Findings will inform the potential for a larger trial and address critical mental health and violence prevention needs in conflict-affected Afghan communities.

Detailed description

Background: A large portion of Afghanistan's population, particularly children, has endured prolonged conflict, poverty, and displacement, leading to significant psychological distress. As children grow into adolescence and adulthood, this distress often manifests in mental health symptoms and an increased likelihood of violent behaviours. With limited mental health professionals and strong stigma around mental health in Afghanistan, culturally adapted, evidence-based interventions are needed.

Objective: The study aims to explore the feasibility and acceptability of culturally adapted mental health intervention Problem Management Plus with an additional Emotional Processing module (PM+ EP), in reducing psychological distress in young Afghans. The primary objective is to assess the feasibility of delivering this intervention in Afghanistan and its acceptability by the target communities, and the secondary objective is to assess symptom reduction and behavioural change.

Methods: This is a pilot Randomized Control Trial (RCT) with participants aged 16 to 30 in Afghanistan. Eligible participants, young Afghans with high levels of distress and impaired functioning - measured by the Kessler Psychological Distress Scale (K10) -, will be randomized to PM+ EP (n=30) or the waiting group (n=30). The participants will be evaluated through self-report questionnaires at three time points; baseline (T1), four weeks later immediately post-intervention (T2), and 3 months post-intervention (T3), and through a qualitative interview (Process Evaluation) at the end of the study. Outcomes will include measures of anxiety and depression (HSCL-25), aggressive behaviours (AGQ), PTSD symptoms (PCL-5), and daily functioning (WHODAS 2.0).

Analysis: This study will assess the feasibility and acceptability of culturally adapted PM+ EP in Afghanistan and explore the relationship between mental health symptoms and violence among young Afghans. It will be the first to evaluate the feasibility of PM+ EP with this population and could pave the way for a large define RCT examining the effectiveness this approach, should the results show promise.

Interventions

  • Behavioral Problem Management Plus with Emotional Processing module
    PM+ EP comprises of Problem Management Plus, an evidence-based low intensity psychological intervention developed by the World Health Organization (WHO), with an additional Emotional Processing module specifically to address psychological distress related to trauma exposure. The core of the intervention is designed for adults impaired by distress in communities exposed to conflict and adversity; it consists of CBT techniques that have been adapted for communities that do not have good availabili

Primary outcome measures

  • Reduction in psychological distress symptoms among participants, as measured by scientific scale HSCL-25. [Time frame: Pre-intervention until 3 months post-intervention]
  • Reduction in psychological distress symptoms among participants, as measured by scientific scale DSM-5 (PCL-5). [Time frame: Pre-intervention until 3 months post-intervention]
  • Reduction in psychological distress symptoms among participants, as measured by scientific scale WHODAS 2.0. [Time frame: Pre-intervention until 3 months post-intervention]
Secondary outcome measures (2)
  • Participant-Reported Changes in Attitudes Toward Violence and Perceived Impact of PM+ EP on Mental Health and Behavior. [Time frame: 3 months post-intervention]
  • Analysis of relationship between mental health and violence, as measured by scientific scale AGQ. [Time frame: Pre-intervention until 3 months post-intervention]

Eligibility criteria

Inclusion criteria

  • Psychological Distress, measured at >15 on the Kessler Psychological Distress Scale (K10)
  • Afghan nationality
  • Age between 16 and 30
  • Ability to read and write in Dari

Exclusion criteria

  • Imminent suicide risk
  • Experiencing psychosis
  • Neurological or cognitive disabilities

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Non-randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Other

Study locations

Afghanistan · 1 center
  • Peace of Mind Association (PoMA) — Kabul

Identifiers

NCT: NCT06980441 · 1378139

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗