The RESPCCT Study: Community-led Development of a Person-Centered Instrument to Measure Health Equity in Perinatal Services

Author:

Vedam Saraswathi1,Stoll Kathrin1,Tarasoff Lesley2,Phillips-Beck Wanda3,Lo Winnie4,MacDonald Kate5,Metellus Ariane1,Rost Michael6,Scott Muriel7,Hodge Karen89,Korchinski Mo10,van der Pijl Marit11,Alonso Cristina12,Clark Esther13,Tatum Ali1,Olson Rachel14,Xie Kathy,Decker Mary15,Wenzel Karolina1,Roine Alexandra1,Hall Wendy1

Affiliation:

1. University of British Columbia

2. University of Toronto

3. First Nations Health and Social Secretariat of Manitoba

4. NHS England

5. Paralegal Candidate

6. University of Basel

7. Cross Lake Health Services

8. Sunny Hill Health Centre

9. Parent with Spinal Cord Injury, Research Consultant

10. Unlocking the Gates Service Society

11. Amsterdam University Medical Centers

12. Center of Complex Interventions

13. Royal Alexandra Hospital

14. Firelight Research Group, Inc

15. Fraser Health

Abstract

While Canadian maternal mortality rates suggest widespread access to high-quality care, perinatal health care outcomes and care experiences among pregnant people in Canada vary widely, particularly among communities that have been historically oppressed, excluded, and marginalized. The lack of patient-oriented research and measurement in perinatal services led to the RESPCCT (Research Examining the Stories of Pregnancy and Childbirth in Canada Today) Study which used a community participatory action research (CPAR) approach to examine experiences of pregnancy and childbirth care. In this paper, we describe co-creation of a person-centered survey instrument that measures respect, disrespect and mistreatment during pregnancy-related care of individuals with diverse identities, backgrounds and circumstances. The study was co-led by a Community Steering Council alongside a multi-disciplinary group of researchers and clinicians, and pilot tested by service users from across Canada. The final survey instrument includes items that assess respectful care across 17 domains, including validated measures of autonomy, respect, mistreatment, trauma, and discrimination. It also captures information about respondents’ identities, backgrounds, circumstances, access to care, provider type, and outcomes. A total of 6096 individuals participated in the survey. We describe how we implemented CPAR best practices, strengths, challenges, and lessons learned for instrument development in reproductive justice research.

Publisher

University of Cincinnati - Office of Innovation and Community Engagement

Reference107 articles.

1. Participatory Research: Working with Vulnerable Groups in Research and Practice;J. Aldridge,2016

2. Birth includes us: Development of a community‐led survey to capture experiences of pregnancy care among LGBTQ2S + families;Molly R. Altman;Birth,2023

3. Development of a Measure of Postpartum PTSD: The City Birth Trauma Scale;Susan Ayers;Frontiers in Psychiatry,2018

4. Indigenous maternal health and health services within canada: A scoping review;Meagan Bacciaglia;BMC Pregnancy and Childbirth,2023

5. Black Maternal Health Research Re-Envisioned: Best Practices for the Conduct of Research With, For, and By Black Mamas;Black Women Scholars and the Research Working Group of the Black Mamas Matter Alliance;Harvard Law & Policy Review,2019

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