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Swedish unaccompanied youth refugee trial

Evaluation of the Teaching Recovery Techniques community-based intervention for unaccompanied refugee youth experiencing post-traumatic stress symptoms – a randomised controlled study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN47820795
Enrollment
160
Registered
2018-12-20
Start date
2019-01-01
Completion date
Unknown
Last updated
2023-01-30

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

Conditions

Post-traumatic stress disorder (symptoms) Mental and Behavioural Disorders Post-traumatic stress disorder

Interventions

Current intervention as of 04/11/2019: Randomization will use a small-cluster randomization design rather than a single participant randomization design. A new randomization system has

Sponsors

Uppsala University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Current inclusion criteria as of 04/11/2019: Participants eligible for the trial must comply with all of the following at randomization: 1. Aged under 18 years at time of arrival in Sweden (self-reported) 2. Lived in Sweden <6 years 3. Arrived in Sweden unaccompanied 4. Screening positive on the CRIES-8 PTSD screening tool (=17 points) 5. Interest to participate in a group intervention & consent to be randomized 6. Legal guardian consenting to participation if child is aded <15 years Previous inclusion criteria: Participants eligible for the trial must comply with all of the following at randomization: 1. Youth age =14 years 2. Time spent in Sweden < 5 years 3. Arrived in Sweden unaccompanied 4. Screening positive on the CRIES-8 PTSD screening tool (=17 points) 5. Interest to participate in a group intervention & consent to be randomized 6. Legal guardian consenting to participation if child is <15 years

Exclusion criteria

Exclusion criteria: 1. Youth age >20 2. Time spent in Sweden > 5 years 3. Current treatment where therapist advises against intervention 4. Not screening positive on the CRIES-8 PTSD screening tool (=16 points) 5. No interest to participate in a group intervention 6. Legal guardian not consenting to participation if child is <15 years

Design outcomes

Primary

MeasureTime frame
Measured at baseline, 8 and 20 weeks: 1. Post-traumatic stress symptoms, measured using the Children’s Revised Impact of Event Scale (CRIES-8; Perrin, Meiser-Stedman et al. 2005) 2. Depression symptoms, measured using the Patient Health Questionnaire-9 (PHQ-9; Kroenke, Spitzer, & Williams, 2001) 3. Anxiety symptoms, measured using the Generalized Anxiety Disorder-7 (GAD-7; Spitzer, Kroenke, Williams, & Löwe, 2006)

Secondary

MeasureTime frame
Measured at baseline, 8 and 20 weeks: 1. Self-efficacy, measured using the General Self Efficacy Scale (GSE; Schwarzer & Jerusalem, 1995) 2. Wellbeing, measured using the Cantril Ladder (Cantril, 1966; picture from från Sawatzky et al., 1966; modified for use in the present study)

Countries

Sweden

Contacts

Public ContactElin Lampa
elin.lampa@pubcare.uu.se+46 (0)18 471 6574

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 28, 2026