Testing a Modified Family Planning Intervention for Postpartum Women in Uganda
NCT ID: NCT04068870
Last Updated: 2019-08-28
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
PHASE1
20 participants
INTERVENTIONAL
2019-08-05
2020-04-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
NONE
Study Groups
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Contraceptive management program
Contraceptive management program
The contraceptive management program will consist of two components: (1) the World Health Organization's contraception protocol and (2) incentivized visits.
Usual care
No interventions assigned to this group
Interventions
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Contraceptive management program
The contraceptive management program will consist of two components: (1) the World Health Organization's contraception protocol and (2) incentivized visits.
Eligibility Criteria
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Inclusion Criteria
* 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
18 Years
45 Years
FEMALE
Yes
Sponsors
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African Community Center for Social Sustainability
UNKNOWN
University of Vermont
OTHER
Responsible Party
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Sarah Heil
Professor
Principal Investigators
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Sarah Heil, PhD
Role: PRINCIPAL_INVESTIGATOR
University of Vermont
Locations
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Nakaseke District Hospital
Nakaseke, , Uganda
Countries
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Central Contacts
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Facility Contacts
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John Mundaka, MD
Role: primary
Other Identifiers
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UGPPFP
Identifier Type: -
Identifier Source: org_study_id
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