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The Cesarean Study: Optimizing Cesarean Sections and Improving Patient-Healthcare Provider Trust Using Evidence Informed Recommendations

RecruitingNAAges 18 Years - anyFemaleLund University
NCT07759622 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

Cesarean section (CS) rates have rapidly increased worldwide, with projections suggesting that by 2030, one in every three births will be by CS (1). In Sweden, rates have more than doubled from 9% in the 1990s, to 20% in 2024 (2). While CS can be a life-saving procedure when medically indicated, non-essential CS increase the risk of complications and have been linked to increased maternal morbidity and even death, neonatal respiratory issues, and longer recovery times (3). They also place added strain on already burdened healthcare systems by increasing the use of medical resources and staff capacity. The purpose of this project is to evaluate the use of the "Cesarean Bundle", a three-part intervention designed to improve patient-clinician communication and trust. Primary Aim: To evaluate the impact of the "Cesarean Bundle" in improving patient-clinician communication and trust compare

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📋 Eligibility rules (as published)
Inclusion Criteria: * Pregnant women aged ≥18 years * Referred for consultation regarding planned cesarean section * Able to provide informed consent (with interpreter support if needed) Exclusion Criteria: * Women with an absolute medical indication for cesarean section (e.g., placenta previa), where shared decision-making is not applicable * Women who decline participation in the study components (e.g., surveys/interviews)
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What it tests

  • Cesarean Bundle
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Where

1 site
Skånes university hospital
Malmö, Sweden
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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