Dashboard for Labor Induction

RH
Overseen ByRebecca Hamm, MD MSCE
Age: Any Age
Sex: Female
Trial Phase: Academic
Sponsor: University of Pennsylvania
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

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.

Are You a Good Fit for This Trial?

This trial is for pregnant individuals undergoing labor induction at two specific hospitals. There are no detailed inclusion or exclusion criteria listed, so it appears open to all patients having labor induced at these sites.

Inclusion Criteria

My membranes have not ruptured.
Full term (greater than or equal to 37 weeks gestation)
Singleton gestations
See 1 more

Exclusion Criteria

I have had a cesarean section before.

What Are the Treatments Tested in This Trial?

Trial Overview

The study is testing whether using a dashboard that tracks differences in labor outcomes can help hospital staff follow best practices during labor induction. The research compares results before and after the dashboard is used at two hospitals.

How Is the Trial Designed?

2

Treatment groups

Experimental Treatment

Active Control

Group I: Post periodExperimental Treatment1 Intervention
Group II: Pre periodActive Control1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

University of Pennsylvania

Lead Sponsor

Trials
2,118
Recruited
45,270,000+

Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

Collaborator

Trials
2,103
Recruited
2,760,000+