Supporting postpartum weight loss in women living in deprived communities: design implications for a randomised control trial

Background/Objectives: Pregnancy is a life stage where excess weight gain may occur and the postpartum period is often characterised by weight retention. The aim of the current study was to evaluate the feasibility of undertaking a randomised controlled trial of a weight loss intervention (WeighWell...

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Published in:European journal of clinical nutrition Vol. 65; no. 8; pp. 952 - 958
Main Authors: Craigie, A M, Macleod, M, Barton, K L, Treweek, S, Anderson, A S
Format: Journal Article
Language:English
Published: London Nature Publishing Group UK 01-08-2011
Nature Publishing Group
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Summary:Background/Objectives: Pregnancy is a life stage where excess weight gain may occur and the postpartum period is often characterised by weight retention. The aim of the current study was to evaluate the feasibility of undertaking a randomised controlled trial of a weight loss intervention (WeighWell) in postpartum women living in areas of social disadvantage. Subjects/Methods: The study aimed to recruit 60 women who were not pregnant, 6–18 months postpartum with a body mass index >25 kg/m 2 living in areas of deprivation within Tayside, UK. Recruitment strategies focused on visits to community groups; writing directly to postpartum women living in areas of deprivation and primary care teams who covered the most deprived 15% of the population and advertising in community settings. The 12-week intervention used motivational interviewing techniques to promote an energy deficit diet and increased physical activity, delivered by three face-to-face consultations plus three structured telephone calls. Results: Of 142 women screened, 63 were eligible and 52 (83%) were recruited and randomised to an intervention ( n =29) or comparison group ( n =23). Over the 12-week intervention, body weight changed significantly by −1.6±2.0 kg in the intervention group compared with +0.2±2.2 kg in the comparison group, indicating the potential efficacy of the intervention. Loss to follow-up was 24% in the intervention group and 39% for the comparison group. Conclusions: The findings support the development of a definitive trial that embraces personalised recruitment strategies and the development of approaches to improve retention over a clinically relevant intervention period.
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Alison Kirk, Department of Sport, Culture & the Arts, University of Strathclyde
The WeighWell team
Gary Mires, School of Medicine, University of Dundee
Brian Williams, Social Dimensions of Health Institute, University of Dundee
Annie S. Anderson, Centre for Public Health Nutrition Research, University of Dundee
Robert Fraser, Section of Reproductive & Developmental Medicine, University of Sheffield
Shaun Treweek, Tayside Clinical Trials Unit, University of Dundee
Rose Barbour, School of Nursing & Midwifery, University of Dundee
Anne Ludbrook, Health Economics Research Unit, University of Aberdeen
Andrew Symon, School of Nursing & Midwifery, University of Dundee
Joyce Thompson, Directorate of Public Health, NHS Tayside
ISSN:0954-3007
1476-5640
DOI:10.1038/ejcn.2011.56