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Clinical Trials/NCT07756424
NCT07756424Not yet recruitingNot Applicable

Implementation of a Disparities in Labor Outcomes Dashboard

University of Pennsylvania1 site in 1 country2,300 target enrollmentStarted: October 1, 2026Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Enrollment
2,300
Locations
1
Primary Endpoint
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

Study Overview

Brief Summary

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.

Study Design

Study Type
Interventional
Allocation
Non Randomized
Intervention Model
Sequential
Primary Purpose
Health Services Research
Masking
None

Eligibility Criteria

Sex
Female
Accepts Healthy Volunteers
No

Inclusion Criteria

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

Exclusion Criteria

  • •- prior cesarean

Arms & Interventions

Pre period

No Intervention

Post period

Other

Intervention: Disparities in Labor Outcomes Dashboard (Other)

Outcomes

Primary Outcomes

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

Time Frame: 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."

Secondary Outcomes

  • 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)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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