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Testing a Modified Family Planning Intervention for Postpartum Women in Uganda

University of Vermont logo

University of Vermont

Status and phase

Unknown
Phase 1

Conditions

Contraceptive Usage

Treatments

Behavioral: Contraceptive management program

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

The purpose of this study is to test whether offering incentives to encourage women to attend one-on-one family planning education sessions and offering free, onsite prescription contraceptive methods increases use and continuation of prescription contraception among postpartum women in Uganda. This intervention is modified from one that has been effective outside of Uganda.

Enrollment

20 estimated patients

Sex

Female

Ages

18 to 45 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • 18-45 years of age
  • Not planning on getting pregnant in the next 4 months
  • Less than 3 months postpartum
  • No history of tubal ligation or hysterectomy
  • No recent prescription contraceptive use (no pill, intrauterine device or implant use in the past 7 days or injection use in the past 3 months)
  • Medically eligible to use prescription contraceptives
  • Bringing baby to immunization clinic for the first time

Exclusion criteria

  • Failure to meet the aforementioned inclusion criteria

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

20 participants in 2 patient groups

Contraceptive management program
Experimental group
Treatment:
Behavioral: Contraceptive management program
Usual care
No Intervention group

Trial contacts and locations

1

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Central trial contact

Sarah Heil, PhD

Data sourced from clinicaltrials.gov

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