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Effects of a Health Workforce Capacity Building and Quality Improvement Intervention in Kinshasa

J

Jhpiego

Status

Completed

Conditions

Infant Death
Maternal Death
Stillbirth

Treatments

Behavioral: training for health care workers supplmented by QI teams

Study type

Interventional

Funder types

Other

Identifiers

NCT03363308
OPP1156220

Details and patient eligibility

About

The aim of the study is to evaluate a health workforce capacity building and quality improvement intervention focused on integrated day-of-birth and post-pregnancy care at 16 hospitals in Kinshasa, Democratic Republic of Congo. The intervention package consists of a low-dose, high-frequency (LDHF) training of health workers, support for quality improvement teams, and provision of critical equipment, supplies and drugs within a quality improvement (QI) framework.

Full description

The health workforce capacity building and quality improvement intervention will be implemented in two phases: eight facilities will receive the intervention in phase 1 and the remaining eight facilities will receive the intervention in phase 2.

Objective 1: For objective 2 on facility-based health outcomes, the study design is a cluster-randomized evaluation in phase 1. The intervention's effects will be assessed by comparing an intervention group and a control group of facilities. These will be selected from 16 Kinshasa health facilities. Intervention and control facilities' monthly reported health outcomes will be compared in a 12-month baseline period and 12-month period during and after the intervention implementation (Phase 1) in a difference-in-difference analysis. In Phase 2, all facilities will have their monthly service statistics and health outcomes reviewed for trends in improvement.

Overall, in Phase 1, eight intervention sites will be matched to eight sites serving as controls. In Phase 2, the eight Phase 1 control sites will then receive the same package as the intervention sites in Phase 1. Sites will be stratified by case load, low and high (over 90 births per month), and funding (public or private funding). Within each stratum, prior to start of the intervention, there will be random selection to intervention and control groups to allow for baseline comparability between groups.

Enrollment

250 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Health providers:

    • Currently on the roster of maternity ward providers working at one of the 16 selected facilities at the time of the training module.
    • Willing to attend a Jhpiego clinical training workshop and offer consent as study participant.
    • Age 18 or older.

Exclusion criteria

  • there are no exclusion criteria

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

250 participants in 2 patient groups

Phase 1
Experimental group
Description:
training for health care workers supplemented by QI teams
Treatment:
Behavioral: training for health care workers supplmented by QI teams
Phase 2
No Intervention group

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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