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

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Karolinska Institute

Status

Completed

Conditions

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

Treatments

Behavioral: Culturally Adapted iCBT

Study type

Interventional

Funder types

Other

Identifiers

NCT06102096
KI-CNS-230918

Details and patient eligibility

About

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.

Enrollment

125 patients

Sex

All

Ages

15 to 29 years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

125 participants in 2 patient groups

Active group
Experimental group
Description:
Tailored iCBT for mild to moderate common mental health problems over a period ranging from 6 to 10 weeks.
Treatment:
Behavioral: Culturally Adapted iCBT
Waiting-list
No Intervention group
Description:
control group

Trial contacts and locations

1

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Central trial contact

Shervin Shahnavaz, PhD; Youstina Demetry, MSc

Data sourced from clinicaltrials.gov

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