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The effectiveness of the Triple P programme to support parenting in Dutch preventive child healthcare: a randomised controlled study

The effectiveness of the Triple P programme to support parenting in Dutch preventive child healthcare: a randomised controlled study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON29372
Enrollment
162
Registered
2008-06-11
Start date
2008-09-01
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

Psychosocial problems in children, parenting problems

Interventions

The intervention concerns a maximum of four short (20-30 minutes) contacts with a PCH nurse, based on level 3 of Triple P. It consists of practical advice and coaching on managing a specific behaviour

Sponsors

University Medical Center Groningen (UMCG), University of Groningen, Department of Health Sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Children aged 9-11 years. 2. Total SDQ-score in the sub-clinical range (11-13). 3. Parents recognize / acknowledge detected behavioural or psychosocial problems and are receptive to treatment.

Exclusion criteria

Exclusion criteria: 1. A diagnosis of developmental delay, developmental disorder (e.g. autism), conduct disorder or ADHD. 2. Currently receiving treatment for behavioural problems. 3. A chronic disease for which 3 or more medical consultations in the past 6 months. 4. Parental divorce, death or severe disease of someone to whom the child feels attached (parent, sib, grandparent, friend, nanny) in the past 6 months. 5. Parents in therapy for psychological or relationship problems. 6. Parents unable to read or speak Dutch. 7. Severe and/of general behavioural or emotional problems beyond the scope of the Triple P level 3 intervention. 8. Suspected parental dysfunction as child maltreatment, psychiatric disease, alcohol or drug abuse.

Design outcomes

Primary

MeasureTime frame
The primary outcome of the study is the change in problem behaviour after intervention.

Secondary

MeasureTime frame
Since the intervention aims at parenting as mediator, the secondary outcome of the study is parenting behaviour.

Contacts

Public ContactW. Spijkers

University Medical Center Groningen, University of Groningen, Department of Health Sciences PO Box 196

w.spijkers@med.umcg.nl+31 (0)50 363 8369

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)