Actively Recruiting

Phase Not Applicable
All Genders
Healthy Volunteers
NCT07529704

Evaluation of a Multicomponent Early Intervention for Childhood Obesity Prevention in Vulnerable Families

Led by Helena Vall Roqué · Updated on 2026-04-14

526

Participants Needed

3

Research Sites

117 weeks

Total Duration

On this page

Sponsors

H

Helena Vall Roqué

Lead Sponsor

L

Loyola University

Collaborating Sponsor

AI-Summary

What this Trial Is About

Childhood obesity is a public health concern. Evidence-based, multicomponent, parenting interventions targeting early childhood and adapted to families' socioeconomic context are needed to prevent childhood obesity. This study aims to evaluate the effectiveness of an early intervention in primary care for the prevention of childhood obesity, targeting vulnerable families where the mother and/or the father has overweight or obesity. More specifically, the primary aim of this study is to evaluate the effectiveness the intervention to maintain a healthy weight in children aged 6 months to 3 years, measured by the BMI-for-age z-score at baseline, 6, 12, and 18 months, compared to usual care. The study also aims to evaluate the effectiveness of the intervention, compared to usual care, for: promoting responsive feeding, improving dietary intake, improving parents' and children's physical activity levels, improving parents' eating styles, and improving children's sleep. Finally, the study aims to determine the feasibility of implementing the intervention, and to identify factors influencing change and contextual factors in the implementation process. A pragmatic cluster randomized controlled trial will be conducted. Approximately 526 families (parent-child family dyads) will be recruited, belonging to 76 primary care centers. Primary care centers will be randomly assigned to either an intervention or control group. The intervention has been previously co-designed with families and healthcare professionals, and consists of five weekly sessions and 4 monthly sessions, lasting 2 hours each. It will be delivered by previously trained healthcare professionals or by members of the research team, depending on the preferences and availability of the primary care center professionals. Approximately 38 intervention face-to-face groups will be conducted, one in each primary care center allocated to the intervention group. The study will be conducted in Catalonia, Andalusia and the Balearic Islands (Spain). Effectiveness outcomes include child body mass index (BMI) z-score, parent feeding practices (measured with the Feeding Practices and Structure Questionnaire), child dietary intake (measured with the multiple-pass 24-hour recall), parents' eating behaviours (measured with the Dutch Eating Behavior Questionnaire), child movement (measured with the Movement Behavior Questionnaire), parents' movement behaviours (measured with the Brief Physical Activity Assessment Tool), and child sleep (measured with selected items from the Brief Infant Sleep Questionnaire). Implementation and feasibility outcomes will be assessed through interviews during and at the end of the intervention, and through attendance sheets and a final satisfaction questionnaire. This study will provide pioneering insights into the implementation and effectiveness of this intervention within the public healthcare system in Spain. This will allow the potential implementation in the future at a larger scale.

CONDITIONS

Official Title

Evaluation of a Multicomponent Early Intervention for Childhood Obesity Prevention in Vulnerable Families

Who Can Participate

All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Mothers and/or fathers aged 18 years or older
  • Primary caregivers of a healthy child aged 6 months to 3 years, born at term (≥37 weeks of gestation)
  • At least one parent with overweight or obesity as defined by BMI criteria
  • Families in vulnerability meeting at least two of the following: low education (≤ lower secondary), precarious employment in past year, financial difficulties in past year, unstable housing, single-parent or prolonged absence of one primary caregiver, recent immigration (≤10 years) without stable support or with language barriers
Not Eligible

You will not qualify if you...

  • Parents of a child aged 6 months to 3 years with low birth weight (<2500 g)
  • Parents of a child aged 6 months to 3 years from a multiple birth (e.g., twins, triplets)
  • Parents/caregivers of a child aged 6 months to 3 years with congenital conditions, chronic diseases, or severe disabilities affecting feeding, growth, or study participation
  • Parents or caregivers with severe physical or mental health conditions limiting participation
  • Families planning to move out of the study area during the study period

AI-Screening

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Trial Site Locations

Total: 3 locations

1

Fundación Avedis Donabedian Para la Mejora de la Calidad Asistencial

Barcelona, Catalonia, Spain, 08037

Actively Recruiting

2

Atenció Primària de Mallorca

Palma de Mallorca, Spain, 07002

Actively Recruiting

3

Servicio Andaluz de Salud

Seville, Spain, 41008

Actively Recruiting

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Research Team

H

Helena Vall Roqué, PhD

CONTACT

N

Nuria Hidalgo

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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