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Optimizing Postpartum Contraception in Women With Preterm Births

Optimizing Postpartum Contraception in Women With Preterm Births

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01864629
Enrollment
134
Registered
2013-05-29
Start date
2013-04-30
Completion date
2016-01-31
Last updated
2017-10-26

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

Conditions

Method of Contraception, Preterm Birth Recurrence

Brief summary

The purpose of this study is to examine the effectiveness of focused family planning counseling on the uptake and continuation of highly effective contraceptive methods (defined as the intrauterine device, implant, and both male and female sterilization methods including vasectomy, tubal ligation and Essure) during the postpartum period in women who have recently experienced a preterm delivery. The investigators hypothesize that women with a recent preterm birth (PTB) will be more likely to initiate and continue using a highly effective method of contraception when provided with focused family planning counseling.

Interventions

BEHAVIORALFocused contraception counseling

This intervention will be provided to those randomized to the intervention group only. This counseling will follow a pre-written, structured script describing all contraceptive methods in rank order starting with most effective to least effective in preventing unplanned pregnancy.

Sponsors

University of Utah
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
14 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

* Women who deliver a premature infant that is between the gestational ages of 24 weeks 0 days and 36 weeks 6 days at our institution.

Exclusion criteria

* Women who have delivered via cesarean section and have also had a sterilization procedure at the time of the cesarean section.

Design outcomes

Primary

MeasureTime frame
Use of highly effective methodThree months

Secondary

MeasureTime frame
Pregnancy outcomes12 months, 18 months, 24 months, 36 months
Use of highly effective method12 months, 24 months, 36 months

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026