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Clinical Trials/NCT03333473
NCT03333473
Completed
Not Applicable

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

Jhpiego8 sites in 1 country9,282 target enrollmentNovember 9, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Post-pregnancy Family Planning
Sponsor
Jhpiego
Enrollment
9282
Locations
8
Primary Endpoint
Quality of PPFP counseling
Status
Completed
Last Updated
4 years ago

Overview

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 sectors. The ultimate intent of this investment is to advance and scale up post-pregnancy FP. Programmatic learning will be crucial to understanding what it will take to accelerate post-pregnancy FP in these two countries, and these can later be adapted by other countries with similar settings. Our vision of PPFP Choices can be achieved through the following objectives:

  • Objective 1: Establish a comprehensive program implementation framework for the private sector to embrace post-pregnancy FP
  • Objective 2: Improve the quality of post-pregnancy FP counseling and service provision in both public and private sectors
  • Objective 3: Build evidence and contribute to the literature and programmatic guidance around post-pregnancy FP uptake and continuation in both public and private sectors
  • Objective 4: Ensure effective documentation and strategic dissemination which will benefit post-pregnancy FP introduction and scale-up more broadly

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 private sectors. Jhpiego will implement the study in two counties in Kenya; Meru and Kilifi, and two districts in Indonesia; Brebes and Batang. This study will employ a quasi-experimental design with an intervention and control group. Prior to study start-up, the the intervention group will receive a Jhpiego-designed package of interventions designed to advance post-pregnancy FP in both the public and private sectors. These interventions draw on WHO's Programming Strategies for Postpartum Family Planning, as well as Jhpiego's experience and assessments. After the study is completed, the control groups will receive the same intervention. For the study, a mixed method approach will be used; both quantitative and qualitative data will be collected through Client Quantitative Interviews, Client In-Depth interviews, Focus Group Discussions, Key Informant Interviews, and Facility Assessments.

Registry
clinicaltrials.gov
Start Date
November 9, 2017
End Date
March 16, 2020
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Sponsor
Jhpiego
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • 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)

Exclusion Criteria

  • 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

Outcomes

Primary Outcomes

Quality of PPFP counseling

Time Frame: 3 years

80% of ANC attendees and women receiving postabortion care receive appropriate PPFP counseling prior to discharge compared to baseline in the comparison group.

Clinical competency of service providers in providing all modern FP methods

Time Frame: 3 years

100% of service providers in intervention arm of study are deemed competent and retain competencies to provide all modern FP methods to women during postpartum and postabortion periods.

Secondary Outcomes

  • Health facility-level leadership management and governance skills(3 years)
  • Assessment of individual intervention quality(3 years)
  • Postpartum uptake of LARCs(3 years)

Study Sites (8)

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