F10.1 F12.1
Conditions
Interventions
Group 1: Single-armed (n = 150), 1) Assessments are scheduled pre-intervention (T0), post-intervention (T1), at 3-month (T2) and at 6-month (T3) follow-up. The participants are screened on their subst
Sponsors
Katholische Fachhochschule gGmbH - Deutsches Institut für Sucht- und Präventionsforschung
Eligibility
Sex/Gender
All
Age
18 Years to 35 Years
Inclusion criteria
Inclusion criteria: (1) self-declared refugee background (2) Syria, Iraq, Iran or Afghanistan as the country of origin (3) Age between 18-35 years (4) hazardous use of alcohol and/ or cannabis (AUDIT-score of =5 and <20 for males and =4 and <20 for females and on the CUDIT-R-score of =8 and <12 for all genders) (5) Informed written consent
Exclusion criteria
Exclusion criteria: (1) Country of origin other than Syria, Iraq, Iran or Afghanistan (2) AUDIT-scores <5 or =20 for males and <4 or =20 for females and CUDIT-R-Scores <8 or =12 for all genders (3) In- or out-patient treatment for SUD (except for a group intervention programme that takes place within the consortium) (4) Age younger than 18 or higher than 35 years
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Primary outcomes are the intervention’s feasibility and the target population’s acceptance. These measures are evaluated based on user-data and user-ratings. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary outcome is the intervention’s initial efficacy on the use of alcohol and/ or Cannabis based on a comparison of the 30-days-prevalence between T(0 and T(1). | — |
Countries
Germany
Contacts
Public ContactChristoph Beineke
Deutsches Institut für Sucht- und Präventionsforschung, Katholische Hochschule NRW
Outcome results
None listed