Status:

COMPLETED

Postpregnancy Family Planning Choices in Public and Private Sectors in Kenya and Indonesia

Lead Sponsor:

Jhpiego

Collaborating Sponsors:

Bill and Melinda Gates Foundation

Merck for Mothers

Conditions:

Post-pregnancy Family Planning

Capacity Building of Healthcare Providers

Eligibility:

FEMALE

15-49 years

Phase:

NA

Brief Summary

The primary goal of PPFP Choices is to generate actionable evidence that can be used to increase programmatic activities to address post-pregnancy family planning in the public and private-for-profit ...

Detailed Description

PPFP Choices is an operations research study seeking to examine the barriers and facilitators in offering a full range of FP methods in the immediate post-pregnancy period in both the public and priva...

Eligibility Criteria

Inclusion

  • Kenyan postpartum participant (Enrollment starts at ANC):
  • At least 28 weeks pregnant
  • Plans to deliver at the study facility
  • Aged 15-49 years at enrollment
  • Provides voluntary informed consent
  • Not planning to relocate in the next 12 months
  • Indonesian postpartum participant (Enrollment starts at L\&D):
  • In the immediate postpartum period (within 72 hours, prior to leaving the health facility),
  • Reported having attended ANC within her 3rd trimester (28-weeks pregnant and later),
  • Aged 15-49 years at time of enrollment (Indonesian adolescents aged 15-16 must be married for purposes of the study consent)
  • Provides voluntary informed consent
  • Not planning to relocate in the next 12 months
  • Kenyan and Indonesian postabortion participants:
  • A female in the immediate post-pregnancy treatment phase (within 72 hours in Indonesia, within 48 hours in Kenya, prior to leaving the health facility for treatment of incomplete abortion)
  • Aged 15-49 years at time of enrollment (Indonesian adolescents aged 15-16 must be married for purposes of the study consent)
  • Provides voluntary informed consent
  • Not planning to relocate in the next 6 months

Exclusion

  • Refusal to sign consent form for inclusion in the study
  • Post-delivery baby or mother being treated for trauma or in an intensive care unit

Key Trial Info

Start Date :

November 9 2017

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

March 16 2020

Estimated Enrollment :

9282 Patients enrolled

Trial Details

Trial ID

NCT03333473

Start Date

November 9 2017

End Date

March 16 2020

Last Update

August 17 2021

Active Locations (8)

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Page 1 of 2 (8 locations)

1

RSUD Batang

Batang, Central Java, Indonesia, 51215

2

RSU QOlbu Insan Mulia

Batang, Central Java, Indonesia, 51216

3

Puskesmas Subah

Batang, Central Java, Indonesia, 51262

4

Puskesmas Bawang

Batang, Central Java, Indonesia, 51274