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Traumatized youths in residential care: Exploring the dysregulation of biological stress systems and testing a gamified relaxation intervention.

Traumatized youths in residential care: Exploring the dysregulation of biological stress systems and testing a gamified relaxation intervention. - Traumatized youths in residential care.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON43297
Enrollment
135
Registered
2017-11-15
Start date
2018-01-08
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

autonomic nervous system activity

Interventions

The intervention consists of twee biweekly 15-minute sessions during which participants in the experimental condition play Muse. Participants in the control condition receive TAU
the kind of treatment that is normally being delivered in their situation.
biological stress systems
gamified interventions
residential care
trauma

Sponsors

Radboud Universiteit Nijmegen
Lead Sponsor

Eligibility

Age
2 Years to 17 Years

Inclusion criteria

Inclusion criteria: Both clinical and control sample: - age between 10 and 18 years - being able to speak the Dutch language, to ensure that participants can understand the task instructions and questionnaires, are able to give informed consent or assent, and can participate in the diagnostic interview;Clinical sample: - admitted to residential treatment within youth mental health care, the youth welfare system or care for youth with intellectual disability (ID) - score of 30 or higher on the CRIES-13, a questionnaire to screen for posttraumatic symptoms

Exclusion criteria

Exclusion criteria: Both clinical and control sample: - current or recent (within the last 3 months) EMDR or CBT treatment specifically targeting post-traumatic symptoms - simultaneous participation in another clinical intervention study - psychotic symptoms - negative clinician advice, for example the clinician fears that participation in the study would have negative effects on the participant or that the participants has not the capacities to take part in the study (we have no exclusion criteria based on IQ, to promote external generalizability);Control sample: - presence of any Axis I disorder - current or recent (withing the last 3 months) psychological treatment

Design outcomes

Primary

MeasureTime frame
The focus of this project is on the one hand on the parameters of the HPA axis (i.e. cortisol) and ANS activity (i.e. RSA and PEP), both under resting and social stress conditions. On the other hand, we focus on posttraumatic symptoms, stress, depression, anxiety, and aggression.

Secondary

MeasureTime frame
nvt

Countries

The Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)