Family Planning Knowledge, Attitudes, and Practices of Postpartum Malawian Women

University of North Carolina (UNC) logo

University of North Carolina (UNC)

Status

Completed

Conditions

Contraception

Study type

Observational

Funder types

Other
NIH

Identifiers

NCT01893021
1R25TW009340-01 (U.S. NIH Grant/Contract)
P30AI050410 (U.S. NIH Grant/Contract)
13-1084

Details and patient eligibility

About

The purpose of this study is to understand the family planning needs and practices of postpartum Malawian women, with a focus on long-acting reversible contraception (LARC). Hypotheses: Postpartum women who are older, who have a history of unintended pregnancy, who do not desire another child within 2 years, and who were counseled about LARC during their pregnancy are more likely to have interest in using LARC. Postpartum women who are older are more likely to be aware of LARC methods. HIV+ postpartum Malawian women will have similar knowledge about LARC as postpartum Malawian women who are HIV-.

Full description

This study is a prospective cohort study of 630 postpartum Malawian women. Since our focus is on HIV+ women, HIV+ participants will be recruited in a 1:2 ratio, with a total of 210 HIV+ women and 420 HIV- women. We will recruit in the postpartum ward of Bwaila Maternity Hospital in Lilongwe, Malawi. Participants will complete a baseline survey about demographics, reproductive health history, and family planning knowledge, attitudes, and practices. At 3, 6, and 12 months postpartum, we will complete follow-up phone calls to determine what family planning methods they are using and if they encountered any barriers to receiving LARC if they had been interested in using them.

Enrollment

634 patients

Sex

Female

Ages

18 to 45 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Admission to the postpartum ward at Bwaila Maternity Hospital
  • Live birth ≥28 weeks gestational age within past 4 weeks
  • Fluent in English or Chichewa
  • Age 18-45 years
  • Access to a working phone number
  • Willingness to be contacted by phone for up to one year postpartum

Exclusion criteria

  • History of female sterilization via tubal ligation or hysterectomy
  • Prisoner
  • History of mental disability
  • Serious illness that would prevent participation in the opinion of the Principal Investigator

Trial design

634 participants in 1 patient group

Postpartum Malawian women

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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