The interventions focused on eight lifestyle topics covered in 12 activities (1 h/activity/session) in 7–8-year-old children, and implemented by HPAs over three school academic years. We found that the EdAl programme successfully reduced Wortmannin mTOR childhood OB prevalence in boys by 4.39% and increased the percentage of boys who practise ≥5 after-school PA h/week.18 The EdAl programme needed to be reproduced in other localities, and with other children, to demonstrate the effectiveness of this intervention.19 The outcomes of the EdAl programme supported the feasibility of improving

PA in childhood. However, an educational intervention, such as our EdAl programme implemented by HPAs, also tests complex components such as healthy lifestyles including diet and PA recommendations. Owing to the complexity, such interventions are difficult to rationalise,

standardise, reproduce and administer consistently to all participants.19 There has been one study in the literature that has reproduced its programmes in other locations. Described as the Kiel Obesity Prevention Study (KOPS), the results demonstrated the efficacy and feasibility of implementing new nutritional concepts.20 We tested the reproducibility of the EdAl programme in a geographical area (Terres de l’Ebre) about 80 km away from where the original EdAl programme was designed and implemented. We designed a cluster (town group) randomised controlled trial, the rationale being that since good communications exist between the schools of the same town, this could contribute to schools of the intervention group ‘contaminating’ those of the putative control group. We describe the primary-school-based study to reduce the prevalence of childhood

OB (The EdAl-2 study); the objective remains an intervention to induce healthy lifestyles, including diet and PA recommendations. The study was conducted in 7–8-year-old schoolchildren over three academic years (22 months active school time). Methods The original protocol, rationale, randomisation, techniques and results of the initial EdAl programme have been published in Trials.17 18 The current study (EdAl-2) was conducted in exactly the same way so as to assess whether comparable results could be achieved in a different location. The exact intervention is described Entinostat in more detail in online supplementary file 1, and in this manuscript link. The EdAl-2 study was approved by the Clinical Research Ethical Committee of the Hospital Sant Joan of Reus, Universitat Rovira i Virgili (Catalan ethical committee registry ref 11-04-28/4proj8). This study was registered in Clinical Trials NCT01362023. The protocol conformed to the Helsinki Declaration and Good Clinical Practice guides of the International Conference of Harmonization (ICHGCP). The study followed the CONSORT criteria (see online supplementary additional file 2).