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Supporting postpartum weight loss in women living in deprived communities – design implications for a randomised control trial
BACKGROUND: 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 postpa...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3154650/ https://www.ncbi.nlm.nih.gov/pubmed/21559034 http://dx.doi.org/10.1038/ejcn.2011.56 |
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author | Craigie, Angela M. Macleod, Maureen Barton, Karen L. Treweek, Shaun Anderson, Annie S. |
author_facet | Craigie, Angela M. Macleod, Maureen Barton, Karen L. Treweek, Shaun Anderson, Annie S. |
author_sort | Craigie, Angela M. |
collection | PubMed |
description | BACKGROUND: 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 AND METHODS: The study aimed to recruit 60 women who were not pregnant, 6-18 months postpartum with a BMI >25kg/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 3 face to face consultations plus 3 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 ± 2.0kg in the intervention group compared to +0.2 ± 2.2kg 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. |
format | Online Article Text |
id | pubmed-3154650 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
record_format | MEDLINE/PubMed |
spelling | pubmed-31546502012-02-01 Supporting postpartum weight loss in women living in deprived communities – design implications for a randomised control trial Craigie, Angela M. Macleod, Maureen Barton, Karen L. Treweek, Shaun Anderson, Annie S. Eur J Clin Nutr Article BACKGROUND: 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 AND METHODS: The study aimed to recruit 60 women who were not pregnant, 6-18 months postpartum with a BMI >25kg/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 3 face to face consultations plus 3 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 ± 2.0kg in the intervention group compared to +0.2 ± 2.2kg 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. 2011-05-11 2011-08 /pmc/articles/PMC3154650/ /pubmed/21559034 http://dx.doi.org/10.1038/ejcn.2011.56 Text en Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Craigie, Angela M. Macleod, Maureen Barton, Karen L. Treweek, Shaun Anderson, Annie S. Supporting postpartum weight loss in women living in deprived communities – design implications for a randomised control trial |
title | Supporting postpartum weight loss in women living in deprived communities – design implications for a randomised control trial |
title_full | Supporting postpartum weight loss in women living in deprived communities – design implications for a randomised control trial |
title_fullStr | Supporting postpartum weight loss in women living in deprived communities – design implications for a randomised control trial |
title_full_unstemmed | Supporting postpartum weight loss in women living in deprived communities – design implications for a randomised control trial |
title_short | Supporting postpartum weight loss in women living in deprived communities – design implications for a randomised control trial |
title_sort | supporting postpartum weight loss in women living in deprived communities – design implications for a randomised control trial |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3154650/ https://www.ncbi.nlm.nih.gov/pubmed/21559034 http://dx.doi.org/10.1038/ejcn.2011.56 |
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