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NCT02928341 Clinical Trial

Impact Evaluation of Urban Water Supply Improvements on Cholera and Other Diarrhoeal Diseases in Uvira, Democratic Republic of Congo

Diarrhea Clinical Trial

Official title:
Impact Evaluation of Urban Water Supply Improvements on Cholera and Other Diarrhoeal in Uvira, Democratic Republic of Congo

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02928341
Other study ID # 8913
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date October 2016
Est. completion date December 31, 2021

Study information
Verified date August 2022
Source London School of Hygiene and Tropical Medicine
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of the study is to evaluate the impact of a large-scale urban water supply improvement intervention on cholera and other diarrhoeal diseases. The study uses a step wedge cluster randomised controlled trial (SWcRCT) to measure the effect of the intervention on cholera centre admission rates and confirmed cholera cases. A nested cohort study will examine changes in water-related practices following the intervention.

Recruitment information / eligibility
Status Completed
Enrollment 4556
Est. completion date December 31, 2021
Est. primary completion date December 31, 2021
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Uvira resident admitted to the Uvira Cholera Treatment Centre in Uvira Exclusion Criteria: - Any patients admitted during the period of intervention implementation in each cluster

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Improved water supply

Locations
Country Name City State
Congo, The Democratic Republic of the Centre de Traitement du Cholera, Hôpital General de Reference d'Uvira, Sud-Kivu, République Démocratique du Congo Uvira Sud-Kivu

Sponsors (1)
Lead Sponsor Collaborator
London School of Hygiene and Tropical Medicine

Country where clinical trial is conducted

Congo, The Democratic Republic of the, 

Outcome
Type Measure Description Time frame Safety issue
Primary Admission rate to the Uvira Cholera Treatment Centre 36 months
Secondary Admission rate to the Uvira Cholera Treatment Centre of laboratory confirmed cholera cases 36 months
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