Testing a Modified Family Planning Intervention for Postpartum Women in Uganda
Phase 1
- Conditions
- Contraceptive Usage
- Interventions
- Behavioral: Contraceptive management program
- Registration Number
- NCT04068870
- Lead Sponsor
- University of Vermont
- Brief Summary
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.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- Female
- Target Recruitment
- 20
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
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Exclusion Criteria
- Failure to meet the aforementioned inclusion criteria
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Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Contraceptive management program Contraceptive management program -
- Primary Outcome Measures
Name Time Method Period prevalence use of a prescription contraceptive 6 months after delivery Period prevalence use of a prescription contraceptive
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Nakaseke District Hospital
🇺🇬Nakaseke, Uganda