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Feasibility testing of an internet-based transdiagnostic tailored intervention for refugees

Feasibility testing of an internet-based transdiagnostic tailored intervention for refugees - I-REACH feasibility

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00026911
Enrollment
20
Registered
2021-10-14
Start date
2021-11-15
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

psychological distress

Interventions

Group 1: Participants receive modules of the culturally adapted, transdiagnostic CETA program. This program is called "Al Mamar" (Arabic for path). All participants receive the following modules: Intr

Sponsors

Freie Universität Berlin
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: - Primary diagnosis of a post-traumatic stress disorder (PTSD) according to DSM-5 - Arabic or Farsi language skills (spoken and written) - Internet access (smart phone or computer) - Signed informed consent

Exclusion criteria

Exclusion criteria: - Current psychotic or bipolar disorder - Severe substance use disorder (AUDIT Score> 15 for men,> 13 for women; DUDIT Score> 25) - Acute suicidality (lack of or unclear distancing) - attempted suicide in the past 12 months - Ongoing psychotherapy or unstable medication with psychotropic drugs three months before the start of the study

Design outcomes

Primary

MeasureTime frame
Feasibility of the modules measured by qualitative interviews and client satisfaction questionnaire for internet-based interventions (Client Satisfaction Questionnaire: CSQ-I (Boß et al., 2016)). Participants are invited to participate in an in-depth interview. Here, questions are asked about Al Mamar, as well as barriers to use and facilitating factors for engagement and adherence. In addition, participants will be asked about usability dimensions and possible approaches for widespread implementation of the program in Germany. The questions on usability dimensions are based on the Mobile App Rating Scale in the version for users (uMARS). A subset of 3 to 8 respondents are therapists (online counselors) who are asked about their experiences and usability of the app in an in-depth interview.

Secondary

MeasureTime frame
• Sociodemographic information • Use of health care (developed in the project) • Medication (developed in the project) • General psychological distress, including anxiety and depression • Traumatic life events (developed in the project) • Post-traumatic stress disorder PCL-5 (Krüger-Gottschalk et al., 2017) • Suicidality Suicide Risk Assessment (Arnoldi et al, 2000) • Alcohol & drug use, AUDIT (Babor et al., 1992); DUDIT (Berman et al., 2005) • behavioral addictions (developed in the project) • Quality of Life EQ-5D-5L (Herdman et al., 2011) • Social support (OSSS-3; Kocalevent et al, 2018) • Expectation of self-efficacy (SWE, Schwarzer & Jerusalem, 1999) • Drop-out • Post-migration stressors PMLD-Kurzversion (Short version developed in the project PrevDrop; PMLD: Silove et al., 1998) • Therapeutic relationship WAI (Wilmers et al., 2008) • side effects Negative Effects Questionnaire (Rozental et al., 2019)

Countries

Germany

Contacts

Public ContactCarina Heeke

Freie Universität Berlin

carina.heeke@fu-berlin.de+493083866772

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026