Actively Recruiting

Phase Not Applicable
All Genders
NCT05166850

Preventative Intervention for Cholera for 7 Days

Led by Johns Hopkins Bloomberg School of Public Health · Updated on 2025-12-17

2900

Participants Needed

2

Research Sites

262 weeks

Total Duration

On this page

Sponsors

J

Johns Hopkins Bloomberg School of Public Health

Lead Sponsor

U

University of New Mexico

Collaborating Sponsor

AI-Summary

What this Trial Is About

The first objective of our study is to develop a theory-driven evidence-based targeted water, sanitation, and hygiene (WASH) intervention for household members of diarrhea patients in South Kivu, Democratic Republic of the Congo (DRC) through formative research and community engagement. The second objective is to conduct a randomized controlled trial of 2,320 household members of 580 severe diarrhea patients to evaluate the effectiveness of the developed targeted WASH intervention in terms of: 1. reducing diarrheal diseases household members of cholera and severe diarrhea patients; and 2. increasing WASH behaviors.

CONDITIONS

Official Title

Preventative Intervention for Cholera for 7 Days

Who Can Participate

All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diarrhea patients presenting with three or more loose stools over a 24h period
  • Having no running water inside of their home
  • Plan to reside in Bukavu for the next 12 months
  • Have a child <5 years in their household
  • Have a working mobile phone in the household
Not Eligible

You will not qualify if you...

  • No one will be excluded because of age, sex, religion, or sexual preference
  • Presenting at the health facility with a fever (COVID-19 prevention)

AI-Screening

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Trial Site Locations

Total: 2 locations

1

General Provincial Reference Hospital of Bukavu

Bukavu, South Kivu, Democratic Republic of the Congo

Actively Recruiting

2

Université Catholique de Bukavu

Bukavu, South Kivu, Democratic Republic of the Congo

Actively Recruiting

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Research Team

C

Christine Marie George, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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