Skip to main content
Clinical Trials/NCT03774797
NCT03774797
Completed
N/A

Immediate Postpartum LARC Implementation: Pilot Study at Michigan Medicine

University of Michigan1 site in 1 country592 target enrollmentSeptember 1, 2018

Overview

Phase
N/A
Intervention
Not specified
Conditions
Pregnancy Related
Sponsor
University of Michigan
Enrollment
592
Locations
1
Primary Endpoint
Patient experience of care
Status
Completed
Last Updated
5 years ago

Overview

Brief 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.

Detailed Description

Based on previous work, the investigators have generated a toolkit to guide the integration of immediate postpartum LARC services into widespread clinical practice. In the proposed work, this toolkit will be used to initiate immediate postpartum LARC services in a single site with low baseline immediate postpartum LARC uptake (Michigan Medicine). The investigators will conduct a feasibility study using mixed methods to assess acceptability and appropriateness of toolkit items; patient experience of care; immediate postpartum LARC utilization rate; and prenatal contraceptive counseling rate.

Registry
clinicaltrials.gov
Start Date
September 1, 2018
End Date
August 16, 2020
Last Updated
5 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Michelle H. Moniz

Assistant Professor

University of Michigan

Eligibility Criteria

Inclusion Criteria

  • Female (patients)
  • Pregnant (patients)
  • Receiving obstetrical care at Michigan Medicine (patients)
  • L\&D provider at Michigan Medicine (providers)

Exclusion Criteria

  • non-English speaking
  • unable to provide informed consent

Outcomes

Primary Outcomes

Patient experience of care

Time Frame: Surveys will be collected from pregnant or postpartum women, during the 6-12 months after implementation of a new protocol for peripartum contraceptive care

Patient online surveys about their experience of care during prenatal visits, hospital stay, or postpartum office visit

Acceptability of implementation process - study site maternity care providers

Time Frame: Surveys will be collected during the 6-12 months after implementation of a new protocol for peripartum contraceptive care

Online survey assessing overall experience of care delivery, acceptability and appropriateness of implementation tools

Appropriateness of implementation process - study site maternity care providers

Time Frame: Surveys will be collected during the 6-12 months after implementation of a new protocol for peripartum contraceptive care

Online survey assessing overall experience of care delivery, acceptability and appropriateness of implementation tools

Appropriateness of care process - patients

Time Frame: Surveys will be collected from pregnant or postpartum women, during the 6-12 months after implementation of a new protocol for peripartum contraceptive care

Online survey assessing experience of care, acceptability and appropriateness of implementation tools

Acceptability of care process - patients

Time Frame: Surveys will be collected from pregnant or postpartum women, during the 6-12 months after implementation of a new protocol for peripartum contraceptive care

Online survey assessing experience of care, acceptability and appropriateness of implementation tools

Secondary Outcomes

  • Appropriateness of implementation toolkit items - patients(Interviews will take place after the survey is completed, during the 6-18 months after implementation of a new protocol for peripartum contraceptive care)
  • Acceptability of implementation toolkit items - providers(Interviews will take place after the survey is completed, during the 6-18 months after implementation of a new protocol for peripartum contraceptive care)
  • Acceptability of implementation toolkit items - patients(Interviews will take place after the survey is completed, during the 6-18 months after implementation of a new protocol for peripartum contraceptive care)
  • Appropriateness of implementation toolkit items - providers(Interviews will take place after the survey is completed, during the 6-18 months after implementation of a new protocol for peripartum contraceptive care)
  • Perinatal contraceptive counseling rate(Measured monthly, up to 24 months after toolkit implementation)
  • Immediate postpartum LARC provision rate(Measured monthly, up to 24 months after toolkit implementation)

Study Sites (1)

Loading locations...

Similar Trials