- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01376336
Trial of Safe Water Storage Among People Living With HIV
Randomized Controlled Trial of Safe Water Storage Among People Living With HIV
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Specific Aim #1: To assess environmental health-related risk and outcomes in a low income peri-urban area of Zambia with a high percentage of people living with HIV/AIDS (PLWHA) (longitudinal observational cohort study and baseline) (Year 1). We will assemble a rich dataset on environmental health-related risk factors in a well defined population, with a focus on household drinking water quality and other water, sanitation, and hygiene (WSH) exposures.
Specific Aim #2: To quantify the WSH-related disease burden among PLWHA, compared with those without HIV/AIDS (individual and household level stratification) (conclusion of baseline). After nine months of data collection, we will perform an initial analysis to determine WSH-related risk by HIV status.
Specific Aim #3: To assess the impact of a water quality intervention on the longitudinal prevalence of Highly Credible Gastrointestinal Illness (HCGI) among PLWHA (randomized controlled trial, year 2). We will conduct a randomised, controlled trial of a safe water storage intervention. We will assess the health impacts of this intervention, with particular focus on the high-risk groups of PLWHA and children under 5 years of age.
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Lusaka, Zambia
- Tropical Gastroenterology and Nutrition Group (TROPGAN), University of Zambia School of Medicine
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Resident of Misisi compound, Lusaka
- Willing to participate in the study
- Is able to give informed consent and does so
- Household has one or more children who are aged 48 months or less at the start of the trial
- The household stores drinking water in the home
Exclusion Criteria:
- Not a resident of Misisi compound, Lusaka
- Unwilling to participate in the study
- Unable to give informed consent or chooses not to participate
- Household does not have one or more children aged 48 months or less at the start of the trial
- The household does not store drinking water in the home
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Safe storage device
This arm will be assigned a safe water storage device.
|
This device is a specially designed water storage container that is intended to reduce the likelihood of re-contamination of household stored drinking water.
|
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No Intervention: Control
This arm of the trial will receive nothing until the end of the trial.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Self-reported diarrheal disease
Time Frame: 18 months
|
Self-reported diarrheal disease information will be collected from each study participant monthly.
These data will be collected monthly with 24 hour, 48 hour, and 7-day recall.
Data will be assessed at 18 months (change from baseline).
|
18 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Weight-for-age z-score
Time Frame: 18 months
|
Weight-for-age z-scores will be taken for all children who are aged less than 48 months ("under 5s") at the start of the trial and monthly during the trial.
These data are useful in tracking short-term wasting, associated with diarrheal disease events.
Data will be assessed at 18 months (change from baseline).
|
18 months
|
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E. coli and total coliforms in household drinking water
Time Frame: 18 months
|
Microbiological indicators of fecal contamination of drinking water at the household level.
Samples will be taken from all households monthly.
Data will be assessed at 18 months (change from baseline).
|
18 months
|
|
Salivary antibody response
Time Frame: 18 months
|
We will collect salivary samples from all consenting individuals (an additional consent form is required) to gather information on IgG and IgA response to specific diarrheal pathogens using a multiplex assay.
This measure provides useful information on both outcomes of interest (diarrheal disease) and exposure to diarrheagenic pathogens.
Samples will be taken at three time points: the beginning, midpoint, and end of the trial.
Data will be assessed at 18 months (change from baseline).
|
18 months
|
Collaborators and Investigators
Collaborators
Investigators
- Principal Investigator: Joe Brown, PhD, London School of Hygiene and Tropical Medicine
Study record dates
Study Major Dates
Study Start
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- QA308
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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