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Culturally Adapted iCBT for Arabic-speaking Refugee and Migrant Youth With Common Mental Health Problems

A Randomized Controlled Trial of a Culturally Adapted iCBT for Arabic-speaking Refugee Youth With Common Mental Health Problems

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06102096
Acronym
RAHA
Enrollment
125
Registered
2023-10-26
Start date
2023-11-27
Completion date
2025-08-31
Last updated
2025-12-12

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

Conditions

Anxiety, Depressive Symptoms, Grief, Insomnia, Marital Relationship, Psychological Trauma, Psychological Well-Being, Resilience, Stress

Keywords

Cognitive behavioral therapy, Psychological well-being, Resilience, Refugee, migrant, youth, mental problems

Brief summary

The aim of the current study is to explore whether culturally adapted internet-based cognitive behavioral therapy is effective in reducing the symptoms of various common mental health problems among Arabic-speaking refugee and migrant youth. We hypothesize that the symptoms of the psychological problems will significantly be reduced among youth who will receive iCBT compared to youth in the control group.

Interventions

BEHAVIORALCulturally Adapted iCBT

A culturally adapted iCBT targeting mild to moderate mental health problems among Arabic-speaking refugee and migrant youth.

Sponsors

Linkoeping University
CollaboratorOTHER_GOV
Karolinska Institutet
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
15 Years to 29 Years
Healthy volunteers
No

Inclusion criteria

* 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 * Has access to a computer, a tablet or a smartphone * Is fluent in reading and writing Arabic * Has the ability to dedicate time to take part in the intervention for 6-10 weeks.

Exclusion criteria

* 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

Design outcomes

Primary

MeasureTime frameDescription
HSCL-25Pre-intervention, during the intervention, immediately after the intervention, 6 months after completion of the interventionAssessment of anxiety and depressive symptoms

Secondary

MeasureTime frameDescription
PHQ-9Pre-intervention, immediately after the intervention, 6 months after completion of the interventionassessment of depressive symptoms
PSYCHLOPSPre-intervention, immediately after the intervention, 6 months after completion of the interventionImpact of problematic area on function
ISIPre-intervention, immediately after the intervention, 6 months after completion of the interventionAssessment of severity of insomnia
PCL-5Pre-intervention, immediately after the intervention, 6 months after completion of the interventionassessment of symptoms of post-traumatic stress disorder
WHO-5Pre-intervention, immediately after the intervention, 6 months after completion of the interventionassessment of subjective psychological well-being
BRSPre-intervention, immediately after the intervention, 6 months after completion of the interventionassessment of resilience
PG-13Pre-intervention, immediately after the intervention, 6 months after completion of the interventionAssessment of prolonged grief disorder

Other

MeasureTime frameDescription
CSQimmediately after the intervention, 6 months after completion of the interventionassessment of the levels of satisfaction of the participant with the intervention

Countries

Sweden

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026