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Recruiting NCT07153198

Promoting Socioemotional Development in Early Childhood: Implementation and Evaluation of the VIPP-SD Parenting Intervention in Portugal

No phase Interventional Parent-Child Relations

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: VIPP-SD.
Who it may be relevant to
Registry conditions: Parent-Child Relations. Basic parameters: 2 years — 5 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Portugal
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

The Video-feedback Intervention to Promote Positive Parenting and Sensitive Discipline (VIPP-SD) is an attachment-based intervention aimed at promoting parental sensitivity and the use of developmentally appropriate, non-coercive discipline strategies (ref). The VIPP-SD intervention integrates the enhancement of parental sensitive responsiveness (Ainsworth et al., 1974) with parent coaching aimed at preventing coercive parent-child interaction cycles (Patterson, 1982) and facilitating sensitive limit-setting practices.ase parental sensitivity and sensitive discipline of the primary parent

Detailed description

Aims and hypotheses

1. The primary aim of the Growing Minds - Strengthening Affective Bonds is to demonstrate the effect of the VIPP-SD on parental sensitivity and sensitive discipline of the primary parent, 8 weeks after the intervention and six months after the intervention. It is expected that sensitivity and sensitive discipline of parents in the intervention condition will significantly increase post-intervention, compared to sensitivity and sensitive discipline of parents in the control condition, who have a similar number of ('dummy') contacts with the interveners. 2. The secondary aim of the study is to examine the efficacy of the intervention in reducing children's behavioral problems, as a function of increased parental sensitivity and the use of sensitive discipline strategies. It is expected that improvements in parenting behaviors resulting from the VIPP-SD intervention will be associated with lower levels of behavioral difficulties in children over time. 3. A third objective of the study is to evaluate the impact of the intervention on broader parenting practices and parental well-being, specifically aiming to mitigate psychopathological symptomatology. The focus will be on reducing symptoms of depression and anxiety among participating parents, in line with evidence suggesting that improvements in parenting sensitivity may contribute to enhanced parental mental health. 4. Finally, the investigators will examine whether the intervention yields economic advantages for society at large. To do this, the investigators will use quality-adjusted life-years (QALYs) as the unit of outcome, allowing to quantify health benefits. By comparing the QALYs associated with the intervention to those resulting from no intervention, the investigators aim to assess the cost-effectiveness and potential return on investment from a societal perspective. This analysis will help determine whether the intervention not only improves family relations but also contributes to economic efficiency by potentially reducing healthcare costs, improving productivity, and enhancing overall societal well-being

Interventions

  • Other VIPP-SD
    Consists of four sessions (with the option of one or two additional booster sessions), held biweekly, depending on the family's needs and availability. Specifically, VIPP-SD addresses disciplinary strategies alongside sensitivity themes through: (1) the differentiation between attachment and exploration behaviors; interpretation of child's behavior and significance of a sensitive response to it; and the importance of sharing emotions (2) the application of distraction and induction as non-coerci

Primary outcome measures

  • Parental sensitivity: Erickson Scales of Parental Sensitivity (ESPS, Egeland, et al., 1990) [Time frame: Data will be collected at pretest, posttest (14 weeks) .]
Secondary outcome measures (5)
  • Strengths & Difficulties Questionnaire" (SDQ Portuguese version Fleitlich et al., 2004) [Time frame: Data will be collected at pretest, posttest (14 weeks) and follow up (12 weeks).]
  • Depression, Anxiety, and Stress Scale - 21 (DASS-21) [Time frame: Data will be collected at pretest, posttest (14 weeks) and follow up (12 weeks).]
  • AQOL-8D (Richardson & Lezzi, 2014) [Time frame: Data will be collected at pretest, posttest (14 weeks) and follow up (12 weeks).]
  • Resource Use Characterization Questionnaire. [Time frame: Data will be collected at pretest, posttest (14 weeks) and follow up (12 weeks).]
  • Child Rearing Practices Report-Questionnaire (CRPR-Q) [Time frame: Data will be collected at pretest, posttest (14 weeks) and follow up (12 weeks).]

Eligibility criteria

Inclusion Criteria: Children will be between 2 and 6 years old, and their parents between must be fluent in Portuguese -

Exclusion Criteria: Children with disabilities, chronic illnesses, or hereditary diseases will be excluded from the study

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Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Prevention

Study locations

Portugal · 1 center
  • Manuela Verissimo — Lisbon

Publications

  • Verissimo M, Guedes M, Fernandes M, Fernandes C, Santos C, Diniz E, Oliveira P, Negrao M, Sampaio F, Bakermans-Kranenburg M. Promoting socioemotional development in early childhood: implementation and evaluation of the VIPP-SD parenting intervention in Portugal. BMC Psychol. 2025 Oct 29;13(1):1190. doi: 10.1186/s40359-025-03431-3. PMID 41163103

Identifiers

NCT: NCT07153198 · I-011-04-25 · Grant nº 325160

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗