Abstract

BackgroundThe World Health Organisation suggests that simplification of the medical abortion regime will contribute to an increased acceptability of medical abortion, among women as well as providers. It is expected that a home-based follow-up after a medical abortion will increase the willingness to opt for medical abortion as well as decrease the workload and service costs in the clinic.Methods/DesignThis study protocol describes a study that is a randomised, controlled, non-superiority trial. Women screened to participate in the study are those with unwanted pregnancies and gestational ages equal to or less than nine weeks. The randomisation list will be generated using a computerized random number generator and opaque sealed envelopes with group allocation will be prepared. Randomization of the study participants will occur after the first clinical encounter with the doctor. Eligible women randomised to the home-based assessment group will use a low-sensitivity pregnancy test and a pictorial instruction sheet at home, while the women in the clinic follow-up group will return to the clinic for routine follow-up carried out by a doctor. The primary objective of the study this study protocol describes is to evaluate the efficacy of home-based assessment using a low-sensitivity pregnancy test and a pictorial instruction sheet 10–14 days after an early medical abortion. Providers or research assistants will not be blinded during outcome assessment. To ensure feasibility of the self-assessment intervention an adaption phase took place at the selected study sites before study initiation. This resulted in an optimized, tailor-made intervention and in the development of the pictorial instruction sheet with a guide on how to use the low-sensitivity pregnancy test and the danger signs after a medical abortion.DiscussionIn this paper, we will describe the study protocol for a randomised control trial investigating the efficacy of simplified follow-up in terms of home-based assessment, 10–14 days after a medical abortion. Moreover, a description of the adaptation phase is included for a better understanding of the implementation of the intervention in a setting where literacy is low and the road-connections are poor.Trial registrationClinicaltrials.gov NCT01827995. Registered 04 May 2013.

Highlights

  • The World Health Organisation suggests that simplification of the medical abortion regime will contribute to an increased acceptability of medical abortion, among women as well as providers

  • In this paper, we will describe the study protocol for a randomised control trial investigating the efficacy of simplified follow-up in terms of home-based assessment, 10–14 days after a medical abortion

  • Abortion represents 8-18% of maternal deaths in India today even though abortion is legal since the Medical Termination of Pregnancy (MTP) Act went into effect in April 1972 [4,5]

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Summary

Introduction

The World Health Organisation suggests that simplification of the medical abortion regime will contribute to an increased acceptability of medical abortion, among women as well as providers. Abortion represents 8-18% of maternal deaths in India today even though abortion is legal since the Medical Termination of Pregnancy (MTP) Act went into effect in April 1972 [4,5]. In 2002, the Drug Controller of India approved the use of mifepristone for the purpose of termination of pregnancy up to 49 days of gestation. In 2008, the Central drug standard control organisation approved the combipack (1 tablet of mifepristone 200 mg and 4 tablets of misoprostol 200 mcg) for medical abortion for up to 63 days of gestation, the MTP Act still state 49 days as the limit for medical abortion [11]. As of 2008 only 3% of qualified abortion providers reported to provide medical abortion, and 23% intended to do so in the future [14]

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