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The HAPPY (Healthy and Active Parenting Programmme for early Years) feasibility randomised control trial: acceptability and feasibility of an intervention to reduce infant obesity.

Authors :
McEachan, Rosemary R. C.
Santorelli, Gillian
Bryant, Maria
Sahota, Pinki
Farrar, Diane
Small, Neil
Akhtar, Shaheen
Sargent, Judith
Barber, Sally E.
Taylor, Natalie
Richardson, Gerry
Farrin, Amanda J.
Bhopal, Raj S.
Bingham, Daniel D.
Ahern, Sara M.
Wright, John
BiB childhood obesity scientific group
Source :
BMC Public Health; 3/1/2016, Vol. 16 Issue 1, p1-15, 15p, 1 Diagram, 3 Charts
Publication Year :
2016

Abstract

<bold>Background: </bold>The prevalence of infant obesity is increasing, but there is a lack of evidence-based approaches to prevent obesity at this age. This study tested the acceptability and feasibility of evaluating a theory-based intervention aimed at reducing risk of obesity in infants of overweight/obese women during and after pregnancy: the Healthy and Active Parenting Programme for Early Years (HAPPY).<bold>Methods: </bold>A feasibility randomised controlled trial was conducted in Bradford, England. One hundred twenty overweight/obese pregnant women (Body Mass Index [BMI] ≥25 kg/m(2)) were recruited between 10-26 weeks gestation. Consenting women were randomly allocated to HAPPY (6 antenatal, 6 postnatal sessions: N = 59) or usual care (N = 61). Appropriate outcome measures for a full trial were explored, including: infant's length and weight, woman's BMI, physical activity and dietary intake of the women and infants. Health economic data were collected. Measurement occurred before randomisation and when the infant was aged 6 months and 12 months. Feasibility outcomes were: recruitment/attrition rates, and acceptability of: randomisation, measurement, and intervention. Intra-class correlations for infant weight were calculated. Fidelity was assessed through observations and facilitator feedback. Focus groups and semi-structured interviews explored acceptability of methods, implementation, and intervention content.<bold>Results: </bold>Recruitment targets were met (~20 women/month) with a recruitment rate of 30 % of eligible women (120/396). There was 30 % attrition at 12 months; 66 % of recruited women failed to attend intervention sessions, but those who attended the first session were likely to continue to attend (mean 9.4/12 sessions, range 1-12). Reaction to intervention content was positive, and fidelity was high. Group clustering was minimal; an adjusted effect size of -0.25 standard deviation scores for infant weight at 12 months (95 % CI: -0.16-0.65) favouring the intervention was observed using intention to treat analyses. No adverse events were reported.<bold>Conclusions: </bold>The HAPPY intervention appeared feasible and acceptable to participants who attended and those delivering it, however attendance was low; adaptations to increase initial attendance are recommended. Whilst the study was not powered to detect a definitive effect, our results suggest a potential to reduce risk of infant obesity. The evidence reported provides valuable lessons to inform progression to a definitive trial.<bold>Trial Registration: </bold>Current Controlled Trials ISRCTN56735429. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
14712458
Volume :
16
Issue :
1
Database :
Complementary Index
Journal :
BMC Public Health
Publication Type :
Academic Journal
Accession number :
113480512
Full Text :
https://doi.org/10.1186/s12889-016-2861-z