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
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
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
Edgar Kestler
Director
World Health Organization
