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Feasibility of Immediate Postpartum Long-acting Reversible Contraception Implementation

NCT03774797 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 592

Last updated 2021-02-12

No results posted yet for this study

Summary

The objective of this study is to test and disseminate tools that drive successful immediate postpartum Long-Acting Reversible Contraception (LARC) implementation. The long-term goal is to reduce unintended pregnancy soon after childbirth by increasing access to immediate postpartum LARC for women who desire it.

Conditions

  • Pregnancy Related

Interventions

OTHER

Implementation Toolkit

Post-implementation patients and providers will be assessed after the implementation toolkit has been used to improve service delivery at the study site.

Sponsors & Collaborators

Principal Investigators

  • Michelle H. Moniz, MD, MSc · University of Michigan

  • Vanessa K. Dalton, MD, MPH · University of Michigan

  • Michelle Heisler, MD, MPH · University of Michigan

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-09-01
Primary Completion
2020-08-16
Completion
2020-08-16

Countries

  • United States

Study Locations

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Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03774797 on ClinicalTrials.gov