Skip to content

An Integrated Community-based Intervention Package in Improving Maternal and Neonatal Health Outcomes

Effectiveness of an Integrated Community-based Intervention Package in Improving Maternal, and Neonatal Health Outcome in Jimma Zone, Southwest Ethiopia: a Cluster Randomized Controlled Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05517577
Acronym
ICBIP-MNH)
Enrollment
624
Registered
2022-08-26
Start date
2022-08-20
Completion date
2023-09-20
Last updated
2023-03-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Birth Preparedness and Complication Readiness Plan, Breastfeeding, Exclusive, Complementary Feeding, Delivery Care, Food Security, Health Care Seeking Behavior, Integrated Community-based Intervention Package, Knowledge, Attitudes, Practice, Morbidity;Newborn, Neonatal Care, Postnatal Care

Keywords

community-based intervention,, maternal,, neonatal,, infant,, health outcome,, randomized controlled trial

Brief summary

This study aims to improve maternal, neonatal and infant health outcomes through an integrated community-based intervention package in Jimma Zone, Southwest Ethiopia.

Detailed description

Background: Maternal, newborn, infant's morbidity and mortality are unacceptably high in sub-Saharan Africa including Ethiopia. Despite considerable efforts made in maternal and child health care, poor maternal, neonatal and child health problems remained a significant public health concern globally and particularly in low and middle-income countries. Community-based Interventions and strategies for improving maternal, newborn, and child health care have been recommended through a continuum of care approach. However, few efforts have been made to identify synergies and integrate different intervention packages across the country. Objective: This study aims to assess the effectiveness of an integrated community-based intervention package in improving maternal, neonatal and infant health outcomes in Jimma Zone, Southwest Ethiopia: a cluster randomized controlled trial. Methods: This is a parallel-arm, single-blind, cluster randomized controlled trial conducted in the Dedo and Seka Chekorsa districts of the Jimma zone. After excluding 10 kebeles from each district to be considered as a buffer zone, we will assign 26 kebeles to the intervention arm and 26 to the control arm. A total of 624 pregnant women in their third trimester who reside in the kebeles assigned to the intervention clusters will be identified and enrolled (312 in intervention and 312 in control groups). The intervention includes Behavioral Change Communication, and male involvement. Various multidisciplinary professionals and experts regularly monitor the overall process of the research and intervention activities. The effect of the intervention in comparison with the routine care will be assessed by fitting mixed-effects linear regression models for the continuous outcomes and mixed-effects linear probability models for the binary outcomes. In all analyses, adjustment will be made for clustering at the kebele level and covariate. All tests will be two-sided and the level of significance will be set at alpha \< 0.05. Budget: A total of 579,888.4ETB will be required. Key words: community-based intervention, maternal, neonatal, infant, health outcome, randomized controlled trial

Interventions

BEHAVIORALBehaviour Change Communication and Male involvement intervention

For the integration of the intervention, it is planned to deliver both service at the same time a by the same means to the women and the men. Pregnant women who fail to take one of the intevetion will not be considered as the participant who received integrated intervention. The intervention will be provided through Women Developmental army (WDA) leaders imparted through gatherings and home visits whereas the Broadcast will be used to strengthen and as a frequent remidinng of the conveyed messages.

Sponsors

Jimma University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
SINGLE (Outcomes Assessor)

Masking description

Allocation concealment will not be done for study participants, as they would certainly know if they are in the intervention group or not. However, data collectors will be blinded to the allocation assignment by not being informed about it, not being part of the trial implementers, and not being inhabitants of any of the kebeles. Moreover, data analysts will be blinded to group allocation.

Intervention model description

First, we selected two districts that have similar characteristics and are adjacent to each other. Both districts have a total of 72 kebeles (the smallest administrative unit), 36 in each district. Then, we chose 20, 10 from each district, kebeles on the boundary of the two districts to act as a buffer zone, to prevent information contamination between the intervention and control clusters. Finally, 26 kebeles in the Dedo district will be assigned to the intervention group while 26 kebeles in the Seka Chekorsa district are assigned to control clusters

Eligibility

Sex/Gender
FEMALE
Age
15 Years to 49 Years
Healthy volunteers
Yes

Inclusion criteria

* Pregnant women in the third trimester * Live in the selected cluster

Exclusion criteria

* Serious illness or clinical complications requiring hospitalization * Maternal death * Newborn death * Stillbirth * Twin gestation * Preterm birth (at \<37 weeks)

Design outcomes

Primary

MeasureTime frameDescription
Neonatal care practicesAt month one after deliveryPrevalence of neonatal care practices
Feeding practiceAt month one after deliveryprevalence of early initiation and exclusive breastfeeding

Secondary

MeasureTime frameDescription
Birth preparedness and complication readiness planAt month one after deliveryProportion of women who had Birth preparedness and complication readiness plan
Neonatal morbidityAt month one after deliveryPrevalence of neonatal morbidity
Skilled deliveryAt month one after deliveryPrevalence of women who delivered at health institution
Maternal feeding practice: At month one after deliveryPrevalence of minimum dietary diversity
Maternal morbidityAt month one after deliveryPrevalence of maternal morbidity

Countries

Ethiopia

Contacts

Primary ContactBekelu Teka, MPH
bekelut23@gmail.com+251 945 031 001
Backup ContactMisra Abdulahi, MPH
misra_ab@yahoo.com+251912010293

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026