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Completed

NCT Number: NCT03290924

Accelerating Newborn Survival in Ghana Through a Low-dose, High-frequency Health Worker Training Approach

This study assesses the effect of a low-dose, high-frequency training approach on long-term evidence-based skill retention among skilled birth attendants and impact on adverse birth outcomes at hospitals in Ghana.

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Key information

About this study

In-service training for skilled birth attendants (SBAs) is one of the most common interventions to address lack of knowledge and skills. However, these training interventions are seldom evaluated for effectiveness in improving learning or performance.

This study study is a cluster-randomized waitlist trial implemented in 40 public and mission hospitals in Ghana. It assesses the effect of a low-dose, high-frequency (LDHF) training approach to update hospital-based SBAs in key evidence-based intrapartum and immediate newborn care practices, using current global guidelines.The LDHF approach includes two 4-day onsite sessions (low dose) with weekly practice sessions, SMS quizzes and reminders, and mentoring via mobile phone and onsite visits between trainings (high frequency). The low-dose sessions include competency acquisition through simulation, case-based learning, and small content packages spread over short time intervals.

Eligible hospitals will be stratified by geographic region and caseload, and then randomly assigned to one of four implementation waves. The pipeline randomization allows for rigorous evaluation while the program is rolled out to all facilities.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

- FACILITIES:

  • Public or faith based hospital
  • At least three skilled birth attendants on staff
  • At least 30 births per month

Exclusion criteria

- FACILITIES:

  • Private hospital
  • Public or faith based hospital with less than three skilled birth attendants on staff
  • Public or faith based hospital with less than 30 births per month

Inclusion criteria

- SERVICE PROVIDERS:

  • Health providers who attend births in participating health facilities and consent to be assessed at the time of enrollment and at several points in time over the study period

Exclusion criteria

- SERVICE PROVIDERS:

  • Health providers who decline to participate

Treatment and study plan

Low dose high frequency health worker training approach

Behavioral
  • Two 4-day training sessions for skilled birth attendants
  • 1-day peer practice coordinator training after first training session
  • Weekly, peer-led practice sessions using MamaNatalie® and NeoNatalie™ anatomic models
  • SMS reminder messages and quizzes
  • Routine telephone calls between master mentors and peer practice coordinators, and between project staff and master mentors
  • Health information officer training
  • Data collection and use training
  • Supply of simulators, newborn resuscitation equipment, and delivery sets

Active Comparison

Behavioral

Training on data collection and reporting

Primary outcomes

  1. institutional twenty-four hour newborn mortality rate

    Time frame: 1 day

    death within 24 hours, or before discharge, of a newborn who breathed at birth

  2. institutional intrapartum stillbirth rate

    Time frame: 1 day

    proportion of all facility births that resulted in intrapartum stillbirth

Secondary outcomes

  1. skilled birth attendant knowledge and skills

    Time frame: Pre-test (before training) - post-test (immediately after training) - endline (12 months)

    score on written and practical examinations on routine and emergency obstetric and newborn care

Sponsors and collaborators

Lead sponsor

Jhpiego

Other

Collaborators

  • Bill and Melinda Gates Foundation

Registry information

Important dates

Study start
2014
Primary completion
2017
Study completion
2017
First posted
Sep 25, 2017
Registry last updated
Sep 25, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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