Postpregnancy Family Planning Choices in Public and Private Sectors in Kenya and Indonesia (PPFP Choices)

Jhpiego

Status: Completed

Conditions: Post-pregnancy Family Planning; Capacity Building of Healthcare Providers

Treatments: Behavioral: Facility-Level Leadership Management and Governance Training; Behavioral: PPFP Clinical and Counseling Skills

Study type: Interventional

Funder types: Other

Identifiers

NCT03333473

IRB00007462

Details and patient eligibility

About

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

Full 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.

Enrollment: 9,282 patients

Sex: Female

Ages: 15 to 49 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

1. Kenyan postpartum participant (Enrollment starts at ANC):

   1. At least 28 weeks pregnant
   2. Plans to deliver at the study facility
   3. Aged 15-49 years at enrollment
   4. Provides voluntary informed consent
   5. Not planning to relocate in the next 12 months

2. Indonesian postpartum participant (Enrollment starts at L&D):

   1. In the immediate postpartum period (within 72 hours, prior to leaving the health facility),
   2. Reported having attended ANC within her 3rd trimester (28-weeks pregnant and later),
   3. Aged 15-49 years at time of enrollment (Indonesian adolescents aged 15-16 must be married for purposes of the study consent)
   4. Provides voluntary informed consent
   5. Not planning to relocate in the next 12 months

3. Kenyan and Indonesian postabortion participants:

   1. 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)
   2. Aged 15-49 years at time of enrollment (Indonesian adolescents aged 15-16 must be married for purposes of the study consent)
   3. Provides voluntary informed consent
   4. Not planning to relocate in the next 6 months

Exclusion criteria

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

Trial design

Primary purpose: Health Services Research

Allocation: Non-Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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9,282 participants in 2 patient groups

Intervention

Experimental group

Description:

The intervention will be applied to health facilities in one district in Indonesia and one county in Kenya. The intervention package will work within existing public and private health facilities to strengthen and assess the effectiveness of facility and provider level PPFP service provision and counseling, and expand method choice for women during antenatal, early labor, and post-pregnancy pre-discharge periods. Training within the intervention package include provider-lever PPFP counseling and service provision (PPFP Clinical and Counseling Skills), as well as provider and facility-level leadership management and governance training (Facility-Level Leadership Management and Governance Training).

Treatment:

Behavioral: Facility-Level Leadership Management and Governance Training

Behavioral: PPFP Clinical and Counseling Skills

Control

No Intervention group

Description:

The health facilities control district in Indonesia and county in Kenya will continue with their standard counseling and service provision throughout the study period. At the conclusion of the study period, the facilities in these areas will receive the same intervention that Intervention facilities received prior to study startup.