- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01368354
Taenia Solium Control Case Study in Zambia (SANTOSOIL)
February 10, 2015 updated by: Chummy S.Sikasunge, University of Zambia
Impact of Community-Led Total Sanitation on the Control of Taenia Solium and Soil Transmitted Helminths in the Eastern Province of Zambia
Summary Diseases due to T. solium and soil transmitted helminths (STHs) are of cosmopolitan distribution and strongly linked with poor sanitation and poverty.
These infections are to a great extent perpetuated by open defecation (OD).
Community-Led Total Sanitation (CLTS) is an approach in which people in rural communities are facilitated to do their own appraisal and analysis, come to their own conclusions, and take their own actions.
To date no rigorous study has been conducted to evaluate the impact of CLTS on the transmission of taeniasis/cysticercosis or STHs, despite the worldwide acclaim which CLTS has received as an approach to improve sanitation.
The overall aim of the study is to contribute to the reduction and subsequent control of T. solium and STH infections through the implementation of CLTS approaches in 1 districts in the Eastern Province of Zambia.
By using CLTS it is hypothesised that toilet acquisition and usage will be increased with a resultant reduction in OD which will in turn reduce the transmission of T. solium and STH infections in the district.
This will be measured by porcine/human cysticercosis prevalence (serological test) and STH infections in humans (quantitative coprological test).
Study Overview
Detailed Description
The study procedure will consist of conducting a pilot study with census to establish the sample frame, shortly followed by a baseline survey during which baseline data on human cysticercosis, porcine cysticercosis (serological test), STH infection prevalence (quantitative coprological test) and anthropometric data (weight, height, arm circumference) will be obtained from the study communities (infected people will receive treatment).
The study communities will be subsequently randomly allocated a status of intervention or control community, and this will determine the point at which CLTS will be administered, but all communities will ultimately receive CLTS.
CLTS will be conducted in intervention communities for 12 months by UNICEF.
A post-intervention survey will follow the 12 month CLTS campaign, and all factors investigated at baseline will be revisited in both intervention and control communities.
The compliance of the CLTS approach will also be measured.
CLTS will be administered to control communities after the completion of the post-intervention survey.
Baseline data will be used to show that the groups are comparable; in the primary analysis the difference between intervention and control at follow up will be analyzed to evaluate the impact of CLTS.
If this intervention can be demonstrated to have an impact on the occurrence and burden of sanitation-linked diseases, then this will provide advocacy for such an approach at policy-maker level.
Study Type
Interventional
Enrollment (Actual)
1197
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Eastern
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Katete district, Eastern, Zambia
- Katete
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Willingness to collaborate
- Accessible by road all year round, even during the wet season
- No current promotion of water, sanitation or hygiene programs
- Rural setting
- Minimum of 10 pig-keeping households (HHs)
- Maximum of 100 HHs
Exclusion Criteria:
- Other ongoing sanitation programmes
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
No Intervention: Control arm
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Active Comparator: CLTS Arm
To induce behavioural changes by confronting the community with their open defecation behaviour.
This will lead to voluntary construction and use of latrines and improved hygiene behaviour.
CLTS involves facilitating a process to inspire and empower rural communities to stop open defecation and to build and use latrines, without offering external hardware subsidies.
Communities are encouraged to appraise and analyse their own sanitation profile, including the extent of open defecation and the spread of faecal-oral contamination.
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CLTS (Community Led Total Sanitation) involves facilitating a process to inspire and empower rural communities to stop open defecation and to build and use latrines, without offering external hardware subsidies.
Communities are encouraged to appraise and analyse their own sanitation profile, including the extent of open defecation and the spread of faecal-oral contamination.
This approach ignites a sense of disgust and share among the community.
The community then collectively realises the impact of its unsanitary practices and this realisation mobilises and initiates collective action to improve the existing sanitation profile.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Number of porcine/human cysticercosis cases (serological test)
Time Frame: One Year
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Blood samples will be collected from humans and pigs before and after intervention in both study arms.
Sera will be tested for presence of circulating cysticercus antigens by a monoclonal antibody based antigen capturing ELISA.
Test result above cut-off is positive.
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One Year
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Number of STH cases in humans
Time Frame: 1 year
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All willing participants will be faecal sampled before and after intervention in both study arm.
Samples will be analysed by a quantitative coprological test (Mc Master method) for measuring presence and levels of soil transmitted helminths (ascaris, trichuris and hookworm).
An EPG (eggs per gram) count will be determined for each worm species.
It is anticipated that CLTS will have an impact (reduction) on faecal contamination of the environment thereby reducing transmission of STH
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1 year
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Chummy Sikasunge, PhD, University of Zambia
- Principal Investigator: Evans K. Mwape, MSc, University of Zambia
- Principal Investigator: Sarah Gabriel, PhD, Institute of Tropical Medicine, Antwerp, Belgium
- Study Chair: Pierre Dorny, PhD, Institute of Tropical Medicine, Antwerp, Belgium
- Principal Investigator: Giveson Zulu, PhD, UNICEF
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
April 1, 2012
Primary Completion (Actual)
January 1, 2015
Study Completion (Actual)
January 1, 2015
Study Registration Dates
First Submitted
June 1, 2011
First Submitted That Met QC Criteria
June 6, 2011
First Posted (Estimate)
June 7, 2011
Study Record Updates
Last Update Posted (Estimate)
February 11, 2015
Last Update Submitted That Met QC Criteria
February 10, 2015
Last Verified
February 1, 2015
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- ICONZ-UNZA
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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