Status:
COMPLETED
Use of a Reproductive Life Planning Tool at the Pediatric Well-Baby Visit With Postpartum Women
Lead Sponsor:
University of Illinois at Chicago
Collaborating Sponsors:
Agency for Healthcare Research and Quality (AHRQ)
Conditions:
Postpartum Period
Contraception Behavior
Eligibility:
FEMALE
15-49 years
Phase:
NA
Brief Summary
Improved access to timely health care and contraception in the postpartum (PP) period is needed to reduce unintended pregnancies and help women achieve desired birth spacing. While the routine 6-week ...
Detailed Description
Specific Aims Aim I. To determine if introducing a self-administered Reproductive Life Planning Tool (RLPT) with postpartum mothers during the 2-month WBV will increase the proportion of women receivi...
Eligibility Criteria
Inclusion
- Postpartum women 15-49 years
- Present with infant for a 2-month WBV at the UIC CYC or PCAC
- Receive healthcare at UIC
- Speak English or Spanish
Exclusion
- Pregnant
- \< 15 years or \> 49 years of age
- Receive healthcare outside the UIC system
- Do not speak English or Spanish
Key Trial Info
Start Date :
January 24 2018
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
September 29 2019
Estimated Enrollment :
129 Patients enrolled
Trial Details
Trial ID
NCT03448289
Start Date
January 24 2018
End Date
September 29 2019
Last Update
October 24 2019
Active Locations (1)
Enter a location and click search to find clinical trials sorted by distance.
1
University of Illinois at Chicago
Chicago, Illinois, United States, 60612