Primärprävention von Depression bei Kindern und Jugendlichen mit einem an Depression erkrankten Elternteil - PRODO

ID

50

DZPG Site

München/Augsburg
General Information
Status

Completed: Recruitment, data collection, and data quality management completed

Description

Since the children of parents who have depression are at greatest risk of developing depression themselves, prevention programmes for this population are a major public health priority. The PRODO study was a randomised controlled trial (RCT) of a family- and group-based CBT prevention program for offspring of parents with depression. We translated and adapted the prevention program Raising Healthy Children (Compas et al., 2009) to the German language and culture. We included children and adolescents (aged 8-17) who have no history of psychiatric disorder and their parents. After the baseline assessment, families are randomised to either the prevention intervention or usual care control condition. The intervention consisted of 8 weekly and 4 monthly sessions in groups of 3-4 families based on three modules: Psychoeducation about parental depression, Coping Strategies for children and Parenting training. Follow-up assessments took place at post-intervention, 9- and 15- months after baseline. Assessments include semi-strcutured clinical interviews with parents and child and questionnaires assessing psychopathology, knowledge of depression, cognitive and emotional factors as well as parenting style. Our hypothesis was that in comparison to the control group who receive no intervention, participants in the experimental group will show a reduced risk of depression as indexed by fewer cases of a depressive episode at 15 months follow-up and fewer psychopathological symptoms at 9- and 15-month follow-up.

Paper

Löchner, Platt et al., (2023): https://bmcpsychiatry.biomedcentral.com/articles/10.1186/s12888-023-04926-2

Trial Number

Clinical Trials NCT02115880

Contact
PI

Prof. Gerd Schulte-Körne

Further PIs

PD Dr. Belinda Platt

Survey Results
Is it an interventional or non-interventional study?
  • Interventional
Specification of study type
  • Parallel
Is it a mono- or multicentric study?

Monocentric

Is it a single or multi country study?

Single

Which country?

Germany

Who are participants?
  • Patients with specific diseases
Which diseases? (ICD-11 classification)
  • Mental, behavioural or neurodevelopmental disorders (06)
Mental, behavioural or neurodevelopmental disorders (ICD-11 classification)
  • Mood disorders
Recruitment setting
  • General population
  • Hospital
  • Outpatient
Target sample size

100

Obtained sample size

100

Start of recruitment

2014

End of recruitment

2017

Minimum age of participants

8

Data sources for the study
  • Interview
  • Questionnaire
Is it planned to share the data?

Yes, there is a plan to make data available

Additional information about data sharing

https://osf.io/q7b6r/

Are further follow-ups planned?

No

Is there consent to re-contact participants?

Yes

Is the implementation of further study components possible?

Yes

View raw data