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Emergency Obstetric and Neonatal Care: The EmONC Trial (EmONC)

Primary Purpose

Maternal Morbidity and Mortality, Stillbirth and Neonatal Mortality

Status
Completed
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
Community Mobilization, HBLSS and facility improvement
Sponsored by
NICHD Global Network for Women's and Children's Health
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Maternal Morbidity and Mortality focused on measuring Pregnancy, Maternal child health, Developing countries, Stillbirth, Neonatal mortality, Maternal mortality, Community intervention, Community mobilization, Home-based Life Saving Skills

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  1. Pregnant women living in and/or delivering within the study cluster
  2. Consent provided

Exclusion Criteria: Eligible pregnant women who do not consent

Sites / Locations

  • University of Buenos Aires
  • IMSALUD / San Carlos University
  • Jawaharlal Nehru Medical College
  • Indira Gandhi Government Medical College
  • Moi University School of Medicine
  • The Aga Khan University
  • University Teaching Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

EMONC: Community mobilization, HBLSS and Facility Improvement

Control

Arm Description

The intervention group received training in community mobilization activities, Home Based Life Saving Skills (HBLSS) and facility improvement.

The control group did not receive an intervention, but collected outcome data through a baseline maternal/newborn birth registry.

Outcomes

Primary Outcome Measures

Composite of either >28 week / >1000 gram stillbirth or 7 day neonatal mortality rate

Secondary Outcome Measures

Maternal mortality rate
Maternal morbidity rates
Stillbirth rate
7-day neonatal mortality rate
28-day neonatal mortality rate
Rates of mothers transported to a referral hospital.
Rates of neonates/infants transported to a referral hospital

Full Information

First Posted
February 21, 2010
Last Updated
November 15, 2013
Sponsor
NICHD Global Network for Women's and Children's Health
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1. Study Identification

Unique Protocol Identification Number
NCT01073488
Brief Title
Emergency Obstetric and Neonatal Care: The EmONC Trial
Acronym
EmONC
Official Title
Evaluation of an Emergency Obstetric and Neonatal Care (EmONC) Intervention Package to Reduce Adverse Pregnancy Outcomes in Low Resource Settings (The EmONC Trial)
Study Type
Interventional

2. Study Status

Record Verification Date
November 2013
Overall Recruitment Status
Completed
Study Start Date
December 2008 (undefined)
Primary Completion Date
October 2011 (Actual)
Study Completion Date
October 2011 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
NICHD Global Network for Women's and Children's Health

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The objective of this cluster randomized controlled trial is to reduce maternal and neonatal mortality by increasing access to and improving the quality of obstetric and neonatal care for pregnant women in study clusters. It is hypothesized that a 25% reduction in >28 week or >1000 gram stillbirth and 7-day neonatal mortality will be achieved in the intervention clusters by a multifaceted Emergency Obstetric Neonatal Care (EmONC) package that will be introduced by an EmONC team.
Detailed Description
Maternal death, stillbirth, early neonatal death, and obstetric fistula are among the most devastating adverse outcomes of pregnancy. Existing interventions could avert the majority of maternal and neonatal deaths; however, those women at greatest risk are least likely to have access to interventions delivered through the formal health care system. In many developing countries, most deliveries in rural areas and a significant number in urban areas are conducted at home without skilled attendance, circumstances which pose a high risk for both mothers and their neonates. The EmONC trial is designed to evaluate a comprehensive intervention encompassing community mobilization to establish and sustain mechanisms of transport and payment and to drive client-oriented emergency obstetrical and neonatal care. The intervention includes teaching recognition of prolonged labor, infection, preeclampsia and hemorrhage, and the use of appropriate stabilization methods by all community birth attendants. In addition, poor access to quality emergency obstetric and neonatal care in a sustainable manner will be addressed. To evaluate the effectiveness of this approach, a cluster-randomized trial is required to assess whether Cluster EmONC teams can work with the community and health care system to reduce adverse pregnancy outcomes in diverse settings where the majority of deliveries occur at home or at a health clinic with few or no available EmONC interventions. To accomplish the intervention, a train-the-trainer approach will be used. Master trainers will facilitate central and regional training sessions for Country trainers organized around the areas of community mobilization; birth attendant skills; and EmONC referral facility improvements. The Country trainers will then support training and related activities in the intervention clusters, predominantly focusing on these three areas. The study population includes pregnant women (and their neonates) living and delivering in the 108 study clusters. The study clusters are largely rural, geographically distinct communities, each of which have approximately 300 annual deliveries. The women will be enrolled at or after 20 weeks gestation and followed to 42 days post delivery. The total duration of the trial will be 24 months.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Maternal Morbidity and Mortality, Stillbirth and Neonatal Mortality
Keywords
Pregnancy, Maternal child health, Developing countries, Stillbirth, Neonatal mortality, Maternal mortality, Community intervention, Community mobilization, Home-based Life Saving Skills

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
267181 (Actual)

8. Arms, Groups, and Interventions

Arm Title
EMONC: Community mobilization, HBLSS and Facility Improvement
Arm Type
Experimental
Arm Description
The intervention group received training in community mobilization activities, Home Based Life Saving Skills (HBLSS) and facility improvement.
Arm Title
Control
Arm Type
No Intervention
Arm Description
The control group did not receive an intervention, but collected outcome data through a baseline maternal/newborn birth registry.
Intervention Type
Behavioral
Intervention Name(s)
Community Mobilization, HBLSS and facility improvement
Other Intervention Name(s)
CM
Intervention Description
Mobilization of the community, with special emphasis on pregnant women and their families, to identify resources and solutions to improve maternal and neonatal mortality, home-based life savings skills (HBLSS) for community birth attendants and facility improvement activities.
Primary Outcome Measure Information:
Title
Composite of either >28 week / >1000 gram stillbirth or 7 day neonatal mortality rate
Time Frame
7 days post delivery
Secondary Outcome Measure Information:
Title
Maternal mortality rate
Time Frame
42 days post delivery
Title
Maternal morbidity rates
Time Frame
42 days post delivery
Title
Stillbirth rate
Time Frame
Delivery
Title
7-day neonatal mortality rate
Time Frame
7 days post delivery
Title
28-day neonatal mortality rate
Time Frame
28 days post delivery
Title
Rates of mothers transported to a referral hospital.
Time Frame
42 days post delivery
Title
Rates of neonates/infants transported to a referral hospital
Time Frame
42 days post delivery

10. Eligibility

Sex
Female
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Pregnant women living in and/or delivering within the study cluster Consent provided Exclusion Criteria: Eligible pregnant women who do not consent
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Robert Goldenberg, MD
Organizational Affiliation
Drexel University College of Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Buenos Aires
City
Buenos Aires
Country
Argentina
Facility Name
IMSALUD / San Carlos University
City
Guatemala City
Country
Guatemala
Facility Name
Jawaharlal Nehru Medical College
City
Belgaum
Country
India
Facility Name
Indira Gandhi Government Medical College
City
Nagpur
Country
India
Facility Name
Moi University School of Medicine
City
Eldoret
Country
Kenya
Facility Name
The Aga Khan University
City
Karachi
Country
Pakistan
Facility Name
University Teaching Hospital
City
Lusaka
Country
Zambia

12. IPD Sharing Statement

Citations:
PubMed Identifier
24090370
Citation
Pasha O, McClure EM, Wright LL, Saleem S, Goudar SS, Chomba E, Patel A, Esamai F, Garces A, Althabe F, Kodkany B, Mabeya H, Manasyan A, Carlo WA, Derman RJ, Hibberd PL, Liechty EK, Krebs N, Hambidge KM, Buekens P, Moore J, Jobe AH, Koso-Thomas M, Wallace DD, Stalls S, Goldenberg RL; EMONC Trial Investigators. A combined community- and facility-based approach to improve pregnancy outcomes in low-resource settings: a Global Network cluster randomized trial. BMC Med. 2013 Oct 3;11:215. doi: 10.1186/1741-7015-11-215.
Results Reference
derived
PubMed Identifier
21156060
Citation
Pasha O, Goldenberg RL, McClure EM, Saleem S, Goudar SS, Althabe F, Patel A, Esamai F, Garces A, Chomba E, Mazariegos M, Kodkany B, Belizan JM, Derman RJ, Hibberd PL, Carlo WA, Liechty EA, Hambidge KM, Buekens P, Wallace D, Howard-Grabman L, Stalls S, Koso-Thomas M, Jobe AH, Wright LL. Communities, birth attendants and health facilities: a continuum of emergency maternal and newborn care (the Global Network's EmONC trial). BMC Pregnancy Childbirth. 2010 Dec 14;10:82. doi: 10.1186/1471-2393-10-82.
Results Reference
derived
Links:
URL
http://gn.rti.org/
Description
The Global Network for Women's and Children's Health Research website contains information regarding the EmONC Trial, as well as other Global Network studies.

Learn more about this trial

Emergency Obstetric and Neonatal Care: The EmONC Trial

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