Actively Recruiting
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
Eligibility Criteria
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
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
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
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
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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