Effectiveness of Shortened Time Interval to Postpartum Visit in Improving Postpartum Attendance

NCT03165838 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 364

Last updated 2017-08-17

No results posted yet for this study

Summary

Due to potential to improve family planning, clinicians are increasingly interested in shortening the time to postpartum visits, but lack an evidence base to change policy.There are no studies that have examined the effectiveness of shortened interval to postpartum visit on attendance rate, contraception use, and rapid repeat of pregnancy (RROP). With this research, the investigators propose to conduct a randomized controlled trial (RCT) to examine the effect of reduced time interval to postpartum visit (3-4 weeks rather than 6-8 weeks) on postpartum visit attendance rate, contraceptive use, and RROP.

Conditions

  • Pregnancy Related
  • Contraception
  • Contraception Behavior
  • Contraception Use

Interventions

BEHAVIORAL

Postpartum Visit 3-4 Weeks

This visit will be the same as the standard of care postpartum visit, but it will be scheduled earlier.

BEHAVIORAL

Postpartum Visit 6-8 Weeks

This standard of care postpartum visit will be scheduled for the standard time interval.

Sponsors & Collaborators

  • Virginia Commonwealth University

    lead OTHER

Principal Investigators

  • Saba W Masho · Virginia Commonwealth University

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2013-11-18
Primary Completion
2016-03-03
Completion
2017-06-20

More Related Trials

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 NCT03165838 on ClinicalTrials.gov