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Clinical Trials/NCT01653626
NCT01653626UnknownNot Applicable

A Matched Pair Cluster-randomized Implementation Study to Measure the Effectiveness of an Intervention Package Aiming to Decrease Perinatal Mortality and Increase Institution-based Obstetric Care Among Indigenous Populations in Guatemala

Hospital San Juan de Dios Guatemala1 site in 1 country1 target enrollmentStarted: July 1, 2012Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Sponsor
Enrollment
1
Locations
1
Primary Endpoint
increase the proportion of institutional deliveries in intervention vs. control clusters

Study Overview

Brief Summary

A matched pair cluster-randomized trial of this intervention package will be conducted in four rural and indigenous districts (Huehuetenango, Quiche, Alta Verapaz and San Marcos) of the Republic of Guatemala, using the health clinic as the unit of randomization. No external intervention is planned for control facilities, although enhanced monitoring, surveillance and data collection will occur throughout the study in all facilities in the four districts.

The package includes 3 interventions: 1) To train health care professionals in emergency obstetric and perinatal care using an innovative high-fidelity, low-tech, in situ, multidisciplinary simulation training curriculum (PRONTO); 2) To design and implement a social marketing strategy that promotes institution-based delivery; and 3) To integrate the role of obstetric nurse and professional midwife in intervention communities to act as liaisons between traditional birth attendants (TBA) and public health units. A fourth, cross-cutting component involves ongoing analysis, monitoring, surveillance and evaluation to strengthen information systems and monitor perinatal outcomes throughout the two years of the study.

Detailed Description

Overall goal

To evaluate the impact of a package of three interventions aiming to increase institution-based delivery and improve emergency obstetric and neonatal care on perinatal mortality, in the four districts with the highest maternal mortality ratios in Guatemala.

Specific objectives

  • Measure the impact of this intervention package on perinatal mortality rates.
  • Measure the impact of this intervention package on the proportion of institution-based delivery among study facilities.
  • Evaluate the processes and success of implementing this combined package of interventions by analyzing process indicators related to the intervention element designed to improve emergency obstetric and neonatal care (PRONTO: emergency obstetric and perinatal training program).

Primary outcome of interest:

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Prevention
Masking
Double (Investigator, Outcomes Assessor)

Eligibility Criteria

Ages
10 Years to 49 Years (Child, Adult)
Sex
Female
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •rural women
  • •indigenous
  • •Facilities at rural area
  • •Clinic attending vaginal deliveries

Exclusion Criteria

  • •Facilities considered too close geographically to risk contamination of intervention to control facilities
  • •Clinics visits by pregnant women who present to intervention or control clinics for reasons other that an obstetric event
  • •Clinic or hospital visits by women who present to intervention or control clinics in the post partum period

Arms & Interventions

package

Experimental

Intervention: package of 3 interventions (Other)

Outcomes

Primary Outcomes

increase the proportion of institutional deliveries in intervention vs. control clusters

Time Frame: Up to 15 months

Secondary Outcomes

  • Decrease perinatal death rate in intervention vs. control clinics(Up to 15 months)

Investigators

Sponsor
Hospital San Juan de Dios Guatemala
Sponsor Class
Other Gov
Responsible Party
Principal Investigator
Principal Investigator

Edgar Kestler

Director

World Health Organization

Study Sites (1)

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