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Psychological Interventions in Children After Road Traffic Accidents or Burns

Psychological Interventions in Children After Road Traffic Accidents or Burns: a Randomized Controlled Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01085370
Acronym
PICARTA-B
Enrollment
108
Registered
2010-03-11
Start date
2010-04-30
Completion date
2013-08-31
Last updated
2014-03-18

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

Conditions

Acute Stress Disorder

Keywords

posttraumatic stress, prevention, children, acute stress disorder due to burn injury or injuries associated with road traffic accidents

Brief summary

Within a randomized controlled design the effects of a brief early psychological intervention (child, parents) after road traffic accidents or burns shall be examined in a sample of 120 children and adolescents (aged 2 to 16 years). During the first seven days after the accident a screening for the risk of developing a posttraumatic stress disorder is conducted to divide the participants into a high risk and a low risk group. Participants with a low risk are excluded from the intervention study but reassessed six months after their accident to validate the screening instrument. After a baseline assessment within 14 days after the accident participants of the high risk group are randomly assigned to an intervention group (n = 60) or a control group (n = 60). The latter receive standard medical care. Children of the intervention group are provided with a brief age appropriate two-session intervention that includes a detailed reconstruction of the accident, psychoeducation and discussion of helpful coping strategies. Both the control and the intervention group are reassessed by blind raters at 3 and 6 months after the accident. Assessment of outcome includes measures of posttraumatic stress symptoms, depression, anxiety, behavior, and health-related quality of life.

Interventions

3 modules: psychoeducation, reconstruction of the trauma, coping skills

Sponsors

University Children's Hospital, Zurich
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
2 Years to 16 Years
Healthy volunteers
No

Inclusion criteria

* Age 2-16 years * Glasgow Coma Scale (GCS) \> 8 * German speaking * Burn accident or road traffic accident

Exclusion criteria

* Glasgow Coma Scale (GCS) \< 9 * more than 2 weeks in the Pediatric Intensive Care Unit * no command of German * previous mental retardation

Design outcomes

Primary

MeasureTime frame
Clinician administered PTSD Scale for Children/Adolescents (CAPS-CA) and Child Posttraumatic Stress Disorder Semistructured Interview and Observational Scale (PTSDSSI)Baseline, 3 months, 6 months post intervention

Secondary

MeasureTime frame
KIDSCREEN-Questionnaire / TAPQOL-Questionnaire (health-related quality of life)Baseline, 3 months, 6 months post intervention
Child behavior Child Behavior Checklist (CBCL)Baseline, 3 months, 6 months post intervention
Child Depression Inventory (CDI)Baseline, 3 months, 6 months post intervention

Countries

Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026