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Randomized Controlled Trial
. 2011 Sep 26:12:208.
doi: 10.1186/1745-6215-12-208.

The effect of participatory women's groups on birth outcomes in Bangladesh: does coverage matter? Study protocol for a randomized controlled trial

Tanja Aj Houweling  1 , Kishwar Azad, Layla Younes, Abdul Kuddus, Sanjit Shaha, Bedowra Haq, Tasmin Nahar, James Beard, Edward F Fottrell, Audrey Prost, Anthony Costello; PCP study team
Collaborators, Affiliations
Randomized Controlled Trial

The effect of participatory women's groups on birth outcomes in Bangladesh: does coverage matter? Study protocol for a randomized controlled trial

Tanja Aj Houweling et al. Trials. .

Abstract

Background: Progress on neonatal survival has been slow in most countries. While there is evidence on what works to reduce newborn mortality, there is limited knowledge on how to deliver interventions effectively when health systems are weak. Cluster randomized trials have shown strong reductions in neonatal mortality using community mobilisation with women's groups in rural Nepal and India. A similar trial in Bangladesh showed no impact. A main hypothesis is that this negative finding is due to the much lower coverage of women's groups in the intervention population in Bangladesh compared to India and Nepal. For evidence-based policy making it is important to examine if women's group coverage is a main determinant of their impact. The study aims to test the effect on newborn and maternal health outcomes of a participatory women's group intervention with a high population coverage of women's groups.

Methods: A cluster randomised trial of a participatory women's group intervention will be conducted in 3 districts of rural Bangladesh. As we aim to study a women's group intervention with high population coverage, the same 9 intervention and 9 control unions will be used as in the 2005-2007 trial. These had been randomly allocated using the districts as strata. To increase coverage, 648 new groups were formed in addition to the 162 existing groups that were part of the previous trial. An open cohort of women who are permanent residents in the union in which their delivery or death was identified, is enrolled. Women and their newborns are included after birth, or, if a woman dies during pregnancy, after her death. Excluded are women who are temporary residents in the union in which their birth or death was identified. The primary outcome is neonatal mortality in the last 24 months of the study. A low cost surveillance system will be used to record all birth outcomes and deaths to women of reproductive age in the study population. Data on home care practices and health care use are collected through interviews.

Trial registration: ISRCTN: ISRCTN01805825.

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Figures

Figure 1
Figure 1
Study areas.
Figure 2
Figure 2
Community action cycle.
Figure 3
Figure 3
Randomisation.
Figure 4
Figure 4
Surveillance system.
See this image and copyright information in PMC

References

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