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CompletedNCT01368354SANTOSOILUpdated Feb 11, 2015

Taenia Solium Control Case Study in Zambia

An interventional study of CLTS in Cysticercosis and Helminthiasis, sponsored by University of Zambia. Completed at 1 site in Zambia. Per ClinicalTrials.gov, last updated 2015-02-11.

Sponsored by University of Zambia · Not applicable, Interventional, and Prevention

Phase
Not applicable
Study type
Interventional
Enrollment
1,197
Allocation
Randomized
Sex
All
01

Study summary

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).

Read the 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.

02

Conditions studied

  • Cysticercosis
  • Helminthiasis

Keywords

  • Community Led Total Sanitation
  • Open Defecation
  • Cysticercosis
  • Soil transmitted helminths
  • Zambia
03

In context

Cysticercosis

10 studies on the registry are indexed under Cysticercosis; 2 are open to participants now.

Browse Cysticercosis studies →

Lead sponsor

University of Zambia is the lead sponsor of 5 studies on the registry; 1 is open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

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

Exclusion Criteria:

  • Other ongoing sanitation programmes
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Single group
Masking
None (open label)
Enrollment
1,197 participants (actual)

Study arms

  • 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.

    Behavioral: CLTS

  • No intervention
    Control arm

Interventions

  • BehavioralCLTS

    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.

06

What researchers measure

Primary outcomes

  1. Number of porcine/human cysticercosis cases (serological test)

    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.

    Time frame: One Year

Secondary outcomes

  1. Number of STH cases in humans

    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

    Time frame: 1 year

07

Study locations

1 site
  • Katete
    Katete district, Eastern, Zambia
08

Timeline

Tracking since Sep 25, 2026
Not marked actual or estimatedDates not marked actual or estimated

The record gives a start of Apr 2012, a primary completion of Jan 2015 and a completion of Jan 2015. It does not say whether these dates are actual or estimated.

How these figures are worked out, and which studies are left out of them.

Registered
Jun 1, 2011
First posted
Jun 7, 2011
Start
Apr 2012
Primary completionActual
Jan 2015
CompletionActual
Jan 2015
Last update
Feb 11, 2015
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Feb 11, 2015, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01368354
Lead sponsor
University of Zambia
Responsible party
Chummy S.Sikasunge (Dr. Chummy Sikalizyo Sikasunge, University of Zambia) — Principal investigator
First posted
Jun 7, 2011
Start date
Apr 2012
Primary completion
Jan 2015
Completion
Jan 2015
Last update
Feb 11, 2015

Study contacts

Chummy Sikasunge, PhD
principal investigator · University of Zambia
Evans K. Mwape, MSc
principal investigator · University of Zambia
Sarah Gabriel, PhD
principal investigator · Institute of Tropical Medicine, Antwerp, Belgium
Pierre Dorny, PhD
study chair · Institute of Tropical Medicine, Antwerp, Belgium
Giveson Zulu, PhD
principal investigator · UNICEF

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Feb 2015. You cannot join it, but the record below documents what was studied.

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