focused and sustained attention, psychofysiological arousal
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Participant is between 12 - 18 years old at the start of the intervention period.Participant receives treatment at one of the participating institutions for specialized youth care and is expected to continue treatment for at least 3 months after the start of the intervention period. Participant has a score of >/= 20 on the 'Kind en Jeugd Trauma Screener '(KJTS) or has been diagnosed with Post Traumatic Stress Disorder (PTSD).Participant speaks and understands Dutch.
Exclusion criteria
Exclusion criteria: Participant has hypersensitivity to sound.Participant is simultaneously participating in another clinical trial.A negative recommendation to participate by an involved clinician (e.g., the involved clinician expects that participation will have a negative effect on the participant).
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The SMAART-J intervention aims to reduce trauma-related symptoms as well as improve arousal regulation, and selective-, and sustained attention functions. The primary outcome measures thus focus on changes in self-reported trauma symptoms, selective- and sustained attention, and arousal through the physiological parameters heart rate variability and skin conductance. | — |
Secondary
| Measure | Time frame |
|---|---|
| Experiences of the client and feasibility of the SMAART-J intervention are secondary outcomes. For this purpose, each participant will fill out a short questionnaire consisting of 5 questions based on a 7-point likert-scale after each session during the intervention period. | — |
Countries
Netherlands
Contacts
Vrije Universiteit