Professional Decision Making in Childbirth. (PDMC)

January 15, 2026 updated by: King's College London

Proessional Decision Making in Childbirth.

The study is an ethnography of clinician decision making in/during childbirth for medical interventions.

Study Overview

Status

Not yet recruiting

Conditions

Detailed Description

Medical interventions in childbirth have risen rapidly in high income countries over the last decade and this global phenomenon is reflected in the United Kingdom with, for example, caesarean section rates in England rising by 17% in the last four years to account for an average 45% of all births in 2024. Medical interventions in childbirth can be essential and have contributed to saving the lives of millions of women and children but the underpinning issues for this large rise in medical interventions in childbirth are not clear although certainly complex and multi - factorial.

The management of risk in childbirth is a central consideration as it is well documented as a key influence for professional decision making. The aim of this research study is to describe and analyse the influences on contemporary professional decisions for medical interventions in childbirth, within which risk - - how it is perceived and negotiated by clinicians and birthing parents, and the context and frameworks that support decisions to intervene or not intervene - is likely to be key.

This is a qualitative observational study with ethnography as the methodology. This approach is appropriate to explore how risk and decision making are constructed in real time contemporary frontline professional practice because it will observe what clinicians actually do (not just what they say they do) and how they create their decisions and rationales through their everyday work and professional and organisational interactions.

This research study is important because it will contribute to further understanding professional decision making for medical interventions in childbirth within a national background context of rising medical interventions, and concern about maternity care. There is not to our knowledge published qualitative research regarding this contemporary context.

This study explores professional decision making in a co - located Obstetric Unit (OU) and Alongside Midwifery Unit (AMU) in one NHS trust. A one study site is not a limitation for an in depth ethnography that will describe and analyse and the influences and complexities of contemporary clinician decision making, and from that build new insights and themes. This study as a qualitative ethnographic study will generate rich in-depth research insights that may be transferable to similar maternity settings.

Study Type

Observational

Enrollment (Estimated)

200

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

    • London
      • London, London, United Kingdom
        • Guy's and St Thomas' NHS Foundation Trust
        • Contact:
        • Contact:
        • Principal Investigator:
          • Deborah Jane Naish, MA. MSc

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

Maternity clinicians in an NHS maternity unit

Description

Inclusion Criteria:

Maternity clinicians (midwives and obstetricians, who are the clinical decision makers in childbirth)

Exclusion Criteria:

Non maternity clinicians (neonatologists, anaesthetists, maternity support workers, who may be influential to decisions made but are not the accountable decision makers)

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Midwives and obstetricians
Decision making for medical interventions in childbirth

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Clinician decisions for medical interventions in childbirth.
Time Frame: From enrolment to 6 months
This is a qualitative ethnographic study collecting qualitative data from observation and interviews with clinicians about their clinical practice and decisions for (or not for) medical interventions in childbirth. Therefore there are no specific quantitative outcome measures included. However ethnographic data will collate decisions (yes/no for medical interventions in childbirth), and code the rationales underpinning these.
From enrolment to 6 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Director: Claire Feeley, PhD, King's College London

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

  • Atkinson, P., Coffey, A., Delamont, S., Lofland, J., &Lofland, L. (2009). Handbook of Ethnography. Sage :London. Brocklehurst, P. & Kwee, A. (2011). Perinatal and maternal outcomes by planned place of birth for healthy women with low risk pregnancies: the Birthplace in England national prospective cohort study. BMJ 2011: 343: d7400 Coxon, K., Scammell, M.& Alaszewski, A. (2012). Risk, pregnancy and childbirth: What do we currently know and what do we need to know? An editorial. Health, Risk & Society. Vol 14, 2012, Issue 6, pages 503 - 510. https://doi.org/10.1080/13698575.2012.709486 Department of Health & Social Care. (2025). New Maternity Inquiry launched to Drive Improvements. Gov.uk Downe, S. & Kingdon, C. (2025).Caesareans are rising fast in the UK - but giving birth is getting worse for women. The Conversation, January 2025 Gulmezoglu, AM., Lawrie, TA., Hezelgrave, N., et al (2016). Interventions to Reduce Maternal and Newborn Morbidity and Mortality. In R. Black, R. Laxminarayan, & M. Temmerman (Eds) (2016) Maternal, Newborn and Child Health: Disease Control Priorities. 3rd Edition (Vol 2). https://www.ncbi.nih.gov/books/NBK361904/doi:10.1596?978-1-4648-0348-2_ch7 Hammersley, M. & Atkinson, P. (2019). Ethnography: Principles in Practice. Routledge: London and New York Healy, S., Humphreys, E., & Kennedy, C. (2016).Midwives' and obstetricians' perceptions of risk and its impact on clinical decision making in labour: An integrative review. Women and Birth Vol 29, Issue 2, April 2016, pages107 - 116 Healy, S., Humphreys, E., & Kennedy, C. (2017). A qualitative exploration of how midwives' and obstetricians' perception of risk affects care practices for low-risk women and normal birth. Women and Birth Vol 30, Issue 5, October 2017, pages 367-375 James, N.(1984). A postscript to nursing. In Bell, C. & Roberts, H. (Eds.) Social Researching: Politics, Problems, Practice. Routledge: London Kirkup, B. (2015). The Report of the Morecambe Bay Investigation. Indep

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Estimated)

June 1, 2026

Primary Completion (Estimated)

December 30, 2026

Study Completion (Estimated)

December 30, 2026

Study Registration Dates

First Submitted

January 5, 2026

First Submitted That Met QC Criteria

January 15, 2026

First Posted (Actual)

January 21, 2026

Study Record Updates

Last Update Posted (Actual)

January 21, 2026

Last Update Submitted That Met QC Criteria

January 15, 2026

Last Verified

December 1, 2025

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • 365059

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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