Evaluation of Immediate Postpartum LARC Implementation Programs

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT03118726

Enrollment

Registered

2017-04-18

Start date

2017-04-13

Completion date

2019-05-31

Last updated

2019-08-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Post Partum Contraception

Keywords

LARC, New Mexico, Contraception

Brief summary

This study will engage hospitals working with the New Mexico Perinatal Collaborative (NMPC) on implementing immediate postpartum long-acting reversible contraception programs. All hospitals in New Mexico interested in implementing immediate postpartum LARC programs will be eligible to participate in the NPMC program evaluation. The study will evaluate the components of this implementation program at several New Mexico hospitals using a stepped wedge design,with components being introduced to each hospital one at a time

Interventions

None listed

Study design

Observational model

COHORT

Time perspective

OTHER

Eligibility

Sex/Gender

ALL

Healthy volunteers

Yes

Inclusion criteria

* Hospital staff: Important individuals at New Mexico hospitals planning to implement immediate postpartum LARC programs, with an emphasis on diversity of administrative perspectives. * If more than 4 potential participants are identified at one institution, additional participants may be included if their participation in the study is likely to contribute additional information (e.g. job title or background is different from other study participants)

Exclusion criteria

\- Inability to speak and read English proficiently

Design outcomes

Primary

Measure	Time frame	Description
Baseline immediate postpartum LARC Implementation	April 2017-December 2018	To determine baseline immediate postpartum LARC implementation in various rural New Mexico hospitals.

Countries

United States

Outcome results