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临床试验/NCT07756424
NCT07756424尚未招募不适用

Implementation of a Disparities in Labor Outcomes Dashboard

University of Pennsylvania1 个研究点 分布在 1 个国家目标入组 2,300 人开始时间: 2026年10月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
入组人数
2,300
试验地点
1
主要终点
Fidelity to a labor induction protocol recommendation to perform all cervical exams performed in latent labor were performed less than or equal to 4.5 hours apart

研究概览

简要总结

This proposal will determine if a Disparities in Labor Outcomes dashboard can be used as an implementation strategy to increase compliance to an evidence-based set of interventions for labor induction in a two-site difference-in-differences study design.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Sequential
主要目的
Health Services Research
盲法
None

入排标准

性别
Female
接受健康志愿者
否

入选标准

  • •full term (greater than or equal to 37 weeks gestation)
  • •singleton gestations
  • •intact membranes
  • •undergoing an induction of labor requiring cervical ripening

排除标准

  • •- prior cesarean

研究组 & 干预措施

Pre period

No Intervention

Post period

Other

干预措施: Disparities in Labor Outcomes Dashboard (Other)

结局指标

主要结局

Fidelity to a labor induction protocol recommendation to perform all cervical exams performed in latent labor were performed less than or equal to 4.5 hours apart

时间窗: from first cervical exam after admission for labor induction until the patient's cervical exam reaches 6cm dilation

Reported as binary - compliant or noncompliant; Time between cervical exams from first exam at admission for labor induction to reaching 6cm dilation will be calculated. If any time between exams is \>=4.5 hours, the outcome will be considered "non-compliant". If all are \<4.5 hours, the outcome will be "compliant."

次要结局

  • Cesarean delivery(single time point, at the time of delivery)
  • Maternal morbidity(from delivery until 30 days postpartum)
  • Time to delivery(as time from start of induction to delivery in hours)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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