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Clinical Trials/NCT01571765
NCT01571765CompletedNot Applicable

Scaling Up Maternal and Child Health In Bushenyi and Rubirizi Districts, UGANDA

University of Calgary1 site in 1 country10,985 target enrollmentStarted: April 2012Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
10,985
Locations
1
Primary Endpoint
Reduced morbidity for children under five years old

Study Overview

Brief Summary

The investigators will assess whether in Bushenyi District in southwestern Uganda, a two year intervention providing comprehensive MNCH programming will:

  • Reduce morbidity and mortality for children under five years old and;
  • Improve access to maternal health services Compared to a control community without MNCH intervention?

Hypothesis:

Comprehensive maternal, newborn and child health programming in Bushenyi Distrcit can have a positive impact on morbidity and mortality for children under five years and will improve access for women to maternal health services which may lead, in the longer term, to decreased maternal mortality.

Detailed Description

A detailed impact assessment will be carried out for the duration of the MNCH training and support initiative in Bushenyi District, using mixed methods. The study will assess 8 of the 11 key core MNCH indicators as identified by CIDA as a priority. Other information to be collected such as demographics and patterns of health care use, and prevalence of disease will help health planners in the districts, and will be helpful in sub analysis and interpretation of findings. The main study will use household surveys in both districts at baseline, midline and endline. Other tools will include pre and post qualitative surveys (FGDs, KII) and analysis of operational data.

The main study group will be representative communities and health centres within Bushenyi District who will receive intervention between 2012 and 2014; Rubirizi District will serve as a control area for this study but will received selected MNCH services starting in 2013 after midline data are collected.

Study Design

Study Type
Interventional
Allocation
Non Randomized
Intervention Model
Parallel
Primary Purpose
Health Services Research
Masking
None

Eligibility Criteria

Ages
15 Years to — (Child, Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • all households living in selected communities; all women 15-49 living in selected communities

Exclusion Criteria

  • Not provided

Arms & Interventions

MNCH programming

Experimental

protocols and training for data collection, referrals, and management for health district. Training in obstetrics, newborn care and management of sick children for health workers, Increased community health promotion such as training of CHWs, health centre management teams and bednet distribution

Intervention: MNCH programming in health district (Other)

no added MNCH activities

No Intervention

Outcomes

Primary Outcomes

Reduced morbidity for children under five years old

Time Frame: 2 years

Secondary Outcomes

  • improved maternal access to health services(24 months)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Jennifer L. Brenner

Clinical Associate Professor

University of Calgary

Study Sites (1)

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