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Accompanied refugeeS In Sweden Trial (ASsIST)

Evaluation of the Teaching Recovery Techniques community-based intervention for accompanied refugee children experiencing post-traumatic stress symptoms – a randomized controlled study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN17754931
Enrollment
160
Registered
2019-06-04
Start date
2019-07-01
Completion date
Unknown
Last updated
2026-01-27

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

Conditions

Post-traumatic stress 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. The target cluster size is 6 participants, bas

Sponsors

Uppsala University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
8 Years to 17 Years

Inclusion criteria

Inclusion criteria: Participants eligible for the trial must comply with all of the following at randomization: 1. Child age =8 years 2. Time spent in Sweden 5 years or less 3. Arrived in Sweden accompanied 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 aged <15 years

Exclusion criteria

Exclusion criteria: 1. Youth age >17 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 aged <15 years

Design outcomes

Primary

MeasureTime frame
Parent- and self-reported child mental health, specifically post-traumatic stress, depression and anxiety symptoms, at pre-intervention (T1), c.8 weeks after randomisation (T2) and c.20 weeks after randomisation (T3): 1. Post-traumatic stress symptoms measured using Children’s Impact of Events Scale (CRIES-13; Perrin, Meiser-Stedman, & Smith, 2005) 2. Depression symptoms measured using 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 pre-intervention (T1), c.8 weeks after randomisation (T2) and c.20 weeks after randomisation (T3): 1. Emotional and behavioural difficulties measured using Strengths and Difficulties Questionnaire (SDQ; Goodman, 1997) 2. Self-efficacy measured using General Self Efficacy Scale (GSE; Schwarzer & Jerusalem, 1995) 3. Wellbeing measured using The Cantril Ladder (Cantril, 1966; picture from 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 18, 2026