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Clinical Trials/NCT03585361
NCT03585361
Completed
Not Applicable

Utilizing All Health System Contacts to Offer Postpartum Family Planning (PPFP) to Pregnant Women and Women Within Twelve Months Postpartum in Ethiopia

Jhpiego6 sites in 1 country776 target enrollmentFebruary 20, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Contraceptive Usage
Sponsor
Jhpiego
Enrollment
776
Locations
6
Primary Endpoint
PPFP uptake
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

This study is investigating whether use of postpartum family planning (PPFP) increases if messages on PPFP and, if desired, PPFP services are integrated into as many contacts as possible between women/couples and the health system during pregnancy and the first year after birth. Health system contacts may be at health facilities (including antenatal, labor and delivery, postnatal, and child immunization visits) or, with Ethiopia's Health Extension Program, at households or health posts in the community.

Detailed Description

This implementation research study used a quasi-experimental, mixed method design with two arms. Two districts in Arsi Zone in Ethiopia's Oromia Region (Hitosa and Lode Hitosa) were selected for the study. In each district, one primary health care unit (PHCU) - a public health center and its satellite health posts - was randomly assigned to the intervention arm and one to the comparison arm. PPFP counseling, services, and documentation were strengthened through training and supervision at health centers in both intervention and comparison PHCUs, consistent with Government of Ethiopia policies and guidelines. Only the intervention arm received the community-based intervention. The community-based intervention involved training Health Extension Workers (HEWs) who staff health posts, make outreach home visits, and support volunteers under the government's Development Army. HEWs were trained on PPFP with a refresher on implant insertion. The community invention also involved giving tools to HEWs and volunteers to help them track women's PPFP preferences and pregnancy risk. The study objectives are to: 1. Assess the effect of systematically integrating PPFP messages into contacts with the health system on uptake of PPFP through 12 months postpartum using a 'dose-response' analysis based on the number of contacts 2. Estimate the added effect of the community-based intervention by comparing uptake of PPFP through 12 months postpartum in intervention and comparison sites 3. Explore the acceptability and feasibility of tracking PPFP and reviewing data at health centers and HEWs and volunteers using record keeping and review processes to track women's decision-making and contraceptive use from pregnancy through 12 months postpartum 4. Explore factors influencing women's/couples' adoption of PPFP during the first 12 months postpartum.

Registry
clinicaltrials.gov
Start Date
February 20, 2017
End Date
May 30, 2018
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Sponsor
Jhpiego
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Pregnant at time of enrollment
  • Willing to give informed consent
  • Provider interviews
  • Providers providing PPFP messages or services in study area
  • Willing to give informed consent

Exclusion Criteria

  • Not pregnant at time of enrollment
  • Living outside study area
  • Provider interviews
  • Not working in antenatal, labor \& delivery, postnatal, or immunization care

Outcomes

Primary Outcomes

PPFP uptake

Time Frame: 12 months after birth

Proportion of interviewed postpartum women who used a modern family planning method within 12 months after giving birth

Secondary Outcomes

  • Method choice(12 months after birth)

Study Sites (6)

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