About this trial
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 approximately 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 four monthly sessions, lasting two 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, the Balearic Islands and Castile and León (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.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
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 a situation of vulnerability, defined as meeting ≥1 of the following criteria: (1) Low educational level of at least one parent (≤ lower secondary education or equivalent); (2) Precarious employment situation during the past year, (3) Perceived financial difficulties during the past year; (4) Insecure or unstable housing conditions; (5) Single-parent family or prolonged absence of one of the primary caregivers; (6) Recent immigration (≤10 years) without a stable support network or with language barriers.
Disqualifiers
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 that may affect feeding, growth, or participation in the study
Parents or caregivers with severe physical or mental health conditions that would limit their ability to participate in the intervention or assessments
Trial design
Parallel
Treatments tested in this trial
Bambú program
BehavioralThe Bambú program is a face-to-face 9-session group-based intervention for parents of children aged 6 months - 3.11 years, where at least one parent has overweight or obesity. Sessions last 2 hours. The first five sessions are delivered weekly and the other four sessions are delivered monthly. Sessions are led by two trained co-leaders (training includes two online sessions and access to a virtual platform with all intervention materials). The program covers six main topics: (1) nutrition: feeding practices and dietary recommendations; (2) physical activity and interactive play; (3) emotion regulation skills and techniques; (4) positive parenting; (5) child sleep; and (6) community support networks. The intervention is structured and includes video visualization and interactive activities. The program has been previously co-designed with families and healthcare professionals aiming to target it to the needs and preferences of vulnerable families with overweight or obesity.
Treatment groups
Trial outcomes
Primary outcomes
Changes from baseline to post-intervention and each follow-up in Body Mass Index (BMI) z-score
The BMI z-scored will be measured using the WHO Child Growth Standards. "At risk for overweight," "overweight," and "childhood obesity" for children under five are defined as BMI z-scores \>1 and ≤2, \>2 and ≤3, or \>3 standard deviations above the median established by WHO growth standards, respectively.
Secondary outcomes
Changes from baseline to post-intervention and each follow-up in child dietary intake
Child dietary intake will be measured using the multiple-pass 24-hour recall, which is a brief interview that will be conducted by healthcare professionals who participate in the project.
Changes from baseline to post-intervention and each follow-up in the Feeding Practices and Structure Questionnaire (FPSQ)
The Feeding Practices and Structure Questionnaire is a self-administered questionnaire that measures parental feeding practices, specifically maternal responsiveness to children's hunger/satiety signals facilitated by routine and structure in feeding. Age- and feeding-stage-appropriate versions of the questionnaire will be administered: (a) the specific FPSQ-28 version for children aged ≥2 years; and (b) the FPSQ version for children aged \<2 years, either the FPSQ milk-feeding version (for caregivers predominantly feeding their child with milk) or the FPSQ (semi-)solids version (for caregivers predominantly feeding their child with solid food. Each subscale is scored separately (range 1-5). No overall total score is calculated. Higher scores indicate greater endorsement of the feeding practice represented by the subscale.
Changes from baseline to post-intervention and each follow-up in the Movement Behavior Questionnaire (MBQ)
The Movement Behavior Questionnaire is a self-administered questionnaire that measures physical activity, screen time and sleep in infants, toddlers and preschoolers. The two age-specific versions of the questionnaire will be used: the MBQ-Baby (MBQ-B) for infants who have not yet reached the walking milestone, and the MBQ-Child (MBQ-C) for children who are able to walk. The closed-ended versions of the MBQ will be used. The questionnaire does not produce a total score. It assesses individual movement behaviours (e.g., tummy time, physical activity, screen time, restrained time, sleep duration). Interpretation depends on the behaviour measured and its alignment with age-specific movement guidelines.
Changes from baseline to post-intervention and each follow-up in Brief Physical Activity Assessment Tool (BPAAT)
The Brief Physical Activity Assessment Tool is a self-administered 2-item questionnaire to identify "inactive" patients in primary care settings. Responses to the two items are combined into a total score ranging from 0 to 8. Higher scores indicate a better outcome, reflecting higher levels of physical activity and adherence to recommended activity guidelines.
Sponsors and contacts
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Helena Vall Roqué
Lead sponsor
Avedis Donabedian Research Institute
Sponsor institution
Loyola University
Collaborator
Andalusian Health Service
Collaborator
Hospital Costa del Sol
Collaborator
Hospital Universitari Son Espases (Palma de Mallorca. Spain)
Collaborator
Primary Care Research Unit of Mallorca, Balearic Islands Health Service, Palma
Collaborator
Research Group on Primary Care and Promotion of the Balearic Islands Community (Grapp-CAIB)
Collaborator
Health Research Institute of the Balearic Islands (IdISBa), Palma
Collaborator
General Directorate of Public Health, Balearic Island, Palma
Collaborator
Public health research group of the Balearic Islands (GISPIB)
Collaborator
Universidad de Burgos
Collaborator
Instituto de Investigación Biosanitaria de Burgos (IBioBurgos)
Collaborator
Gerencia de Atención Primaria de Burgos
Collaborator