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Community-based doula support for migrant women during labour and birth: study protocol for a randomised controlled trial in Stockholm, Sweden (NCT03461640)
  1. Erica Schytt1,2,
  2. Anna Wahlberg2,
  3. Amani Eltayb2,
  4. Rhonda Small2,3,
  5. Nataliia Tsekhmestruk2,
  6. Helena Lindgren2
  1. 1Centre for Clinical Research Dalarna, Uppsala University, Falun, Sweden
  2. 2Women's and Children's health, Karolinska Institute, Stockholm, Sweden
  3. 3Judith Lumley Centre, La Trobe University, Melbourne, Victoria, Australia
  1. Correspondence to Dr Erica Schytt; Erica.Schytt{at}ltdalarna.se

Abstract

Introduction Migrant women consistently rate their care during labour and birth more negatively than non-migrant women, due to communication difficulties, lack of familiarity with how care is provided, and discrimination and prejudicial staff attitudes. They also report being left alone, feeling fearful, unsafe and unsupported, and have poorer birth outcomes than non-migrant women. Community-based doulas (CBDs) are bilingual women from migrant communities who are trained in childbirth and labour support, and who facilitate communication between woman-partner-staff during childbirth. This study protocol describes the design, rationale and methods of a randomised controlled trial that aims to evaluate the effectiveness of CBD support for improving the intrapartum care experiences and postnatal well-being of migrant women giving birth in Sweden.

Methods and analysis A randomised controlled trial. From six antenatal care clinics in Stockholm, Sweden, we aim to recruit 200 pregnant Somali, Arabic, Polish, Russian and Tigrinya-speaking women who cannot communicate fluently in Swedish, are 18 years or older and with no contraindications for vaginal birth. In addition to standard labour support, women are randomised to CBD support (n=100) or no such support during labour (n=100). Trained CBDs meet with women once or twice before the birth, provide emotional, physical and communication support to women throughout labour and birth in hospital, and then meet with women once or twice after the birth. Women’s ratings of the intrapartum care experiences and postnatal well-being are assessed at 6–8 weeks after the birth using selected questions from the Migrant Friendly Maternity Care Questionnaire and by the Edinburgh Postnatal Depression Scale. The intervention group will be compared with the control group using intention-to-treat analyses. ORs and 95% CIs will be estimated and adjustments made if key participant characteristics differ between trial arms.

Ethics and dissemination The study was approved by the Regional Ethical Review Board in Stockholm (approval number: 2018/12 - 31/2).

Trial registration number NCT03461640; Pre-results.

  • migrant women
  • doula support
  • labour and birth
  • intrapartum care experiences
  • postpartum wellbeing
http://creativecommons.org/licenses/by-nc/4.0/

This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.

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Footnotes

  • Contributors ES and RS initiated the study and ES, HL, AE, AW and RS contributed to the planning and design of the study and developed recruitment procedures and questionnaires. ES drafted the manuscript and AW, HL, AE, RS and NT contributed to the writing, and read and approved the final version.

  • Funding Funding for the study has been awarded by the Stockholm County Council (Stockholms Läns Landsting, SLL), and Centre for Clinical Research Dalarna-Uppsala University and Karolinska Institutet have generously contributed with funding for ES and HL.

  • Disclaimer The funding bodies have played no role in the design of the study, nor in data collection, analysis and interpretation of data or in writing the manuscript.

  • Competing interests None declared.

  • Patient consent for publication Not required.

  • Provenance and peer review Not commissioned; externally peer reviewed.

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