Culturally Adapted i-CBT for Farsi/Dari Speaking Migrants

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age15-29
SponsorKarolinska Institutet

About this trial

The aim of this randomized controlled trial (RCT) is to investigate the effectiveness of a culturally adapted internet-based cognitive behavioral therapy (i-CBT) intervention in reducing symptoms of common mental health issues among Farsi/Dari-speaking youth migrants and refugees. Investigator hypothesizes that there will be a significant decrease in psychological symptoms after participants receive the intervention compared to a control group.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Between the ages of 15 and 29.

A score above the cut-off 1.75 on HSCL-25

Has a refugee or migrant background

Has a good and stable internet connection

Disqualifiers

Is suffering from a severe mental illness, such as psychosis or severe depression.

Is suffering from substance abuse

Is undergoing a psychological treatment

Has a high risk of suicide

Trial design

Design model

Parallel

Treatments tested in this trial

  • Culturally adapted i-CBT

    Behavioral

    A culturally and language adapted i-CBT intervention for Farsi/Dari speaking youth migrants and refugees. The intervention targets mild to moderate common mental health problems.

Treatment groups

128 Participants
are divided into 2 treatment groups
Group A: Active groupExperimental treatment 1 intervention
Group B: Waiting-listNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

Hopkins Symptom Checklist-25 (HSCL-25)

Assessment of anxiety and depressive symptoms. HSCL-25 consists of 25 items.Each item is rated on a scale from 1 to 4, where 1 means "Not at all" and 4 means "Extremely".Higher scores indicate a worse outcome, as they reflect greater severity of symptoms.

Time frame
Pre-intervention, up to 5 weeks, immediately after the intervention, 6 months after completion of the intervention

Secondary outcomes

1

Psychological Outcome Profiles (PSYCHLOPS)

Impact of problematic area on function. PSYCHLOPS questionnaire consists of 4 items. These items are designed to capture the patient's main problem, the impact of this problem on their daily life, and their overall well-being. Each question in PSYCHLOPS is scored on a scale from 0 to 5, where 0 indicates no problem and 5 indicates the most severe problem. Higher scores indicate a worse outcome, as they reflect greater severity of problems or distress.

Time frame
Pre-intervention, immediately after the intervention, 6 months after completion of the intervention
2

Insomnia Severity Index (ISI)

Assessment of severity of insomnia symptoms. ISI consists of 7 items, each rated on a scale from 0 to 4.Higher scores indicate a worse outcome, as they reflect more severe insomnia symptoms.

Time frame
Pre-intervention, immediately after the intervention, 6 months after completion of the intervention
3

Prolonged Grief Disorder (PG-13)

Assessment of prolonged grief disorder. The PG-13 consists of 13 items, each rated on a scale from 1 to 5, where 1 means "Not at all" and 5 means "Several times a day". Higher scores indicate a worse outcome, as they reflect more severe symptoms of prolonged grief.

Time frame
Pre-intervention, immediately after the intervention, 6 months after completion of the intervention
4

Posttraumatic Stress Disorder Checklist (PCL-5)

Assessment of symptoms of post-traumatic stress disorder. The PCL-5 consists of 20 items, each rated on a scale from 0 to 4. The total score ranges from 0 to 80. Higher scores indicate a worse outcome, as they reflect greater severity of PTSD symptoms.

Time frame
Pre-intervention, immediately after the intervention, 6 months after completion of the intervention

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Karolinska Institutet

Lead sponsor

Linkoeping University

Collaborator