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Trial registered on ANZCTR
Registration number
ACTRN12614000680662
Ethics application status
Approved
Date submitted
16/06/2014
Date registered
27/06/2014
Date last updated
27/06/2014
Type of registration
Retrospectively registered
Titles & IDs
Public title
Integration of deworming with a water, sanitation and hygiene program for the prevention of intestinal parasites in Timor-Leste
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Scientific title
A cluster randomised controlled trial comparing the impact of a water, sanitation and hygiene (WASH) intervention integrated with albendazole distribution versus albendazole distribution alone, on reinfection with intestinal parasites in rural communities in Timor-Leste
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Secondary ID [1]
284809
0
Nil
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Universal Trial Number (UTN)
Nil
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Trial acronym
WASH for WORMS
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Soil transmitted helminths – Trichuris trichiura, Ascaris lumbricoides, hookworms (Necator americanus and Ancylostoma duodenale)
292186
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Intestinal protozoa (Giardia duodenalis, Entamoeba histolytica, Strongyloides sp., Cryptosporidium sp.)
292187
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Anaemia
292188
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Stunting
292189
0
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Wasting
292190
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Condition category
Condition code
Public Health
292526
292526
0
0
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Epidemiology
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Infection
292527
292527
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0
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Studies of infection and infectious agents
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
The intervention to be evaluated in this proposal will involve provision of access to improved water and sanitation and improving related hygiene practices, which will be supported by WaterAid, Australia (WA). The sanitation component is based on the Community Led Total Sanitation approach with WA giving technical support to the construction of latrines. Furthermore, WA staff will lead the construction of piped water from springs/streams to storage tanks/tapstands in villages; and local partner NGOs will promote hand washing with soap. The hygiene intervention will be based on 2-3 visits to each village shortly after the triggering takes place, to promote hand washing with soap using several methods including a hygiene promotion film, establishing a children group and developing a hygiene promotion drama, and a female group. Monitoring visits will happen monthly until the completion of the water intervention and every 6 months for 2 years after the water infrastructure is completed.
All communities (control and intervention arm) will receive mass chemotherapy with one oral tablet of albendazole 400mg every six months for 2 years, starting when 80% of the households have sanitation. Albendazole intake will be directly observed by the field workers delivering the pills who will be working under the supervision of a registered nurse.
Questionnaires including questions on access to water, sanitation and hygiene practices will be used to monitor the progression of the implementation of the integration; and will be part of field work at each 6 monthly visit.
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Intervention code [1]
289598
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Prevention
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Intervention code [2]
289645
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Treatment: Drugs
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Comparator / control treatment
Control communities will receive mass chemotherapy with one oral tablet of albendazole 400mg every six months for 2 years.
Albendazole intake will be directly observed by the field workers delivering the pills who will be working under the supervision of a registered nurse.
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Control group
Active
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Outcomes
Primary outcome [1]
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Reduction in prevalence of infection with A. lumbricoides. Infection status will be assessed by real time PCR on a stool sample obtained at each visit.
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Assessment method [1]
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Timepoint [1]
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Each six-monthly follow-up (Follow-up (FU) 1=6 months after 1st alb distribution), FU2, FU3, FU4=2yrs after 1st albendazole (ALB) distribution).
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Primary outcome [2]
292387
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Reduction in prevalence of infection with T. trichiura.
Infection status will be assessed by real time PCR on a stool sample obtained at each visit.
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Assessment method [2]
292387
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Timepoint [2]
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Each six-monthly follow-up (FU1=6 months after 1st alb distribution), FU2, FU3, FU4=2yrs after 1st ALB distribution).
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Primary outcome [3]
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Reduction in prevalence of infection with hookworms (undifferentiated)
Infection status will be assessed by real time PCR on a stool sample obtained at each visit.
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Assessment method [3]
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Timepoint [3]
292388
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Each six-monthly follow-up (FU1=6 months after 1st alb distribution), FU2, FU3, FU4=2yrs after 1st ALB distribution).
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Secondary outcome [1]
308849
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Reduction in prevalence of G. duodenalis.
Infection status will be assessed by real time PCR on a stool sample obtained at each visit.
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Assessment method [1]
308849
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Timepoint [1]
308849
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At each six-monthly follow-up (FU1=6 months after 1st alb distribution), FU2, FU3, FU4=2yrs after 1st ALB distribution).
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Secondary outcome [2]
308850
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Reduction in prevalence of E. histolytica.
Infection status will be assessed by real time PCR on a stool sample obtained at each visit.
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Assessment method [2]
308850
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Timepoint [2]
308850
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At each six-monthly follow-up (FU1=6 months after 1st alb distribution), FU2, FU3, FU4=2yrs after 1st ALB distribution).
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Secondary outcome [3]
308851
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Changes in the ratio of numbers of people infected with the hookworms A. duodenalis, N. Americanus and A. ceylanicum.
Species differentiation will be done by real time PCR on a stool sample obtained at each visit
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Assessment method [3]
308851
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Timepoint [3]
308851
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At each six-monthly follow-up (FU1=6 months after 1st alb distribution), FU2, FU3, FU4=2yrs after 1st ALB distribution).
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Secondary outcome [4]
308852
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Changes in mean haemoglobin concentration (measured with a portable analyser).
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Assessment method [4]
308852
0
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Timepoint [4]
308852
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At baseline and at the annual follow-ups (FU2=1 year after 1st ALB distribution and FU4=2 years after 1st ALB distribution)
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Secondary outcome [5]
308853
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Changes in height-for-age z-scores
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Assessment method [5]
308853
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Timepoint [5]
308853
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At baseline and at the annual follow-ups (FU2=1 year after 1st ALB distribution and FU4=2 years after 1st ALB distribution)
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Secondary outcome [6]
308854
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Changes in weight-for-age z-score
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Assessment method [6]
308854
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Timepoint [6]
308854
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At baseline and at the annual follow-ups (FU2=1 year after 1st ALB distribution and FU4=2 years after 1st ALB distribution)
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Secondary outcome [7]
308855
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Changes in height-for-weight z-scores.
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Assessment method [7]
308855
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Timepoint [7]
308855
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At baseline and at the annual follow-ups (FU2=1 year after 1st ALB distribution and FU4=2 years after 1st ALB distribution)
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Secondary outcome [8]
308856
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Reductions in the mean intensity of infection (calculated as the average number of eggs per gram of faeces) of A. lumbricoides. Intensity of infection assessed by real-time quantitative PCR.
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Assessment method [8]
308856
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Timepoint [8]
308856
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At each six-monthly follow-up (FU1=6 months after 1st alb distribution), FU2, FU3, FU4=2yrs after 1st ALB distribution).
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Secondary outcome [9]
308857
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Reductions in the mean intensity of infection (calculated as the average number of eggs per gram of faeces) of T. trichiura . Intensity of infection assessed by real-time quantitative PCR
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Assessment method [9]
308857
0
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Timepoint [9]
308857
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At each six-monthly follow-up (FU1=6 months after 1st alb distribution), FU2, FU3, FU4=2yrs after 1st ALB distribution).
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Secondary outcome [10]
308858
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Reductions in the mean intensity of infection (calculated as the average number of eggs per gram of faeces) of hookworms (undifferentiated) . Intensity of infection assessed by real-time quantitative PCR
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Assessment method [10]
308858
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Timepoint [10]
308858
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At each six-monthly follow-up (FU1=6 months after 1st alb distribution), FU2, FU3, FU4=2yrs after 1st ALB distribution).
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Eligibility
Key inclusion criteria
Resident of each selected community
Informed consent obtained
Over 1 year of age
Not in the 1st trimester of pregnancy
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Minimum age
1
Years
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Maximum age
No limit
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Sex
Both males and females
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Can healthy volunteers participate?
Yes
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Key exclusion criteria
Not a resident of the community
No informed consent
Outside of the specified age range
Pregnant in the 1st trimester
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Study design
Purpose of the study
Prevention
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
All members of the randomly selected communities, from whom informed consent was obtained will be enrolled in the study provided they are older than one year of age and not pregnant in the 1st trimester. Allocation is not concealed.
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
This is a cluster randomised trial. Cluster units will be small rural villages in Manufahi district, Timor-Leste. Random number generation will be used in MS excel to randomise villages/communities into control or intervention groups.
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Masking / blinding
Open (masking not used)
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Who is / are masked / blinded?
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Intervention assignment
Parallel
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Other design features
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Phase
Not Applicable
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Type of endpoint/s
Efficacy
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Statistical methods / analysis
Sample size calculations were for the primary outcome Using A. lumbricoides as an example, given an assumed baseline prevalence of 60% and a reduction in prevalence at the 6-month follow-up of 25% in the control group (albendazole chemotherapy only), we estimate a control-group prevalence of 45%. Using data from a recent national helminth survey in the Philippines (Leonardo et al., unpublished), we estimate an intracluster correlation coefficient for prevalence of A. lumbricoides of 0.19. We have assumed a fixed population size in each village; 150 people, of whom 120 participate with a subsequent 10% loss to follow-up. To determine whether the community-based hygiene and sanitation programme results in a 50% reduction of the follow-up prevalence compared to the control group (i.e., to 22.5%), with a power of 80% and a=0.05, we would need to include 12 villages in each of the intervention and control arms. Similar results were obtained for the other STH. Thus, we will enrol 2,880 people, located in 24 villages, randomised 1:1 between the intervention and control arms.
Primary and secondary outcomes will be calculated and compared across both arms of the trial using mixed effects multivariate regression models that account for clustering of participants in villages.
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Recruitment
Recruitment status
Active, not recruiting
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Date of first participant enrolment
Anticipated
28/05/2012
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Actual
28/05/2012
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Date of last participant enrolment
Anticipated
18/10/2013
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Actual
18/10/2013
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
2880
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Accrual to date
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Final
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Recruitment outside Australia
Country [1]
6151
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Timor-Leste
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State/province [1]
6151
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Manufahi
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Funding & Sponsors
Funding source category [1]
289422
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Government body
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Name [1]
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National Health and Medical Research Council (NHMRC)
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Address [1]
289422
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NHMRC, GPO Box 1421, Canberra ACT 2601
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Country [1]
289422
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Australia
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Funding source category [2]
289423
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Charities/Societies/Foundations
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Name [2]
289423
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WaterAid Australia
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Address [2]
289423
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Level 7, 176 Wellington Parade, East Melbourne, VIC 3002 Australia
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Country [2]
289423
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Australia
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Primary sponsor type
Individual
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Name
Archie Clements
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Address
ANU College of Medicine, Biology and Environment
The Australian National University
Building 62 Mills Road
Canberra ACT 0200
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Country
Australia
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Secondary sponsor category [1]
288105
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Individual
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Name [1]
288105
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James McCarthy
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Address [1]
288105
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QIMR Berghofer Medical Research Institute
University of Queensland
Dept. of Infectious Diseases,
Royal Brisbane and Womens Hospital
Herston Rd Herston
QLD 4029 Australia
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Country [1]
288105
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Australia
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Secondary sponsor category [2]
288106
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Individual
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Name [2]
288106
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Rebecca J Traub, BSc BVMS (Hons) PhD
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Address [2]
288106
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Faculty of Veterinary Science
University of Melbourne
Parkville VIC 3052
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Country [2]
288106
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Australia
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Secondary sponsor category [3]
288107
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Individual
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Name [3]
288107
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Darren Gray
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Address [3]
288107
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ANU College of Medicine, Biology and Environment
The Australian National University
Building 62 Mills Road
Canberra ACT 0200
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Country [3]
288107
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Australia
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Secondary sponsor category [4]
288108
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Individual
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Name [4]
288108
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Jim Black
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Address [4]
288108
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Nossal Institute for Global Health
Melbourne School of Population and Global Health
Level 4, Alan Gilbert Building
161 Barry St, Carlton, VIC, 3010
Australia
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Country [4]
288108
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Australia
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Secondary sponsor category [5]
288109
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Individual
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Name [5]
288109
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Ross Andrews
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Address [5]
288109
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Menzies School of Health Research
PO Box 41096
Casuarina NT 081
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Country [5]
288109
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Australia
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Secondary sponsor category [6]
288110
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Individual
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Name [6]
288110
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Susana Nery
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Address [6]
288110
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School of Population Health, University of Queensland
Level 4, Public Health Building;
Herston Road; Herston 4006; Queensland; Australia
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Country [6]
288110
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Australia
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Other collaborator category [1]
278001
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Individual
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Name [1]
278001
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Martha Morrow
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Address [1]
278001
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Nossal Institute for Global Health
Level 4, Alan Gilbert Building
Corner of Barry and Grattan Streets (161 Barry St)
The University of Melbourne
Carlton, Victoria, 3010
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Country [1]
278001
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Australia
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Other collaborator category [2]
278002
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Individual
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Name [2]
278002
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Andrey Vallely
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Address [2]
278002
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University of New South Wales
The CFI Building
Corner Boundary and West Streets
Darlinghurst NSW 2010
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Country [2]
278002
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Australia
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Other collaborator category [3]
278003
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Individual
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Name [3]
278003
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Gail Williams
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Address [3]
278003
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School of Population Health, University of Queensland
Level 4, Public Health Building;
Herston Road; Herston 4006; Queensland; Australia
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Country [3]
278003
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Australia
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
291180
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The University of Queensland – Medical Research Ethics Committee (MREC)
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Ethics committee address [1]
291180
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Cumbrae Stewart Bldg (72) UQ Research and Innovation The University of Queensland Brisbane St Lucia QLD 4072
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Ethics committee country [1]
291180
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Australia
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Date submitted for ethics approval [1]
291180
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Approval date [1]
291180
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13/07/2011
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Ethics approval number [1]
291180
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2011000734
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Ethics committee name [2]
291181
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Gabinete Pesquisa e Desenvolvimento Saude, Ministerio da Saude, Timor-Leste
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Ethics committee address [2]
291181
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Instituto Nacional de Saude Comorro Dili Timor-Leste
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Ethics committee country [2]
291181
0
Timor-Leste
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Date submitted for ethics approval [2]
291181
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Approval date [2]
291181
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09/08/2011
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Ethics approval number [2]
291181
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MS-CHRD/VIII/2011/51
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Summary
Brief summary
Soil-transmitted helminths (STH) are most prevalent in communities lacking adequate clean water, sanitation and hygiene (WASH). Deworming programmes with anthelminthic drugs are highly effective in reducing morbidity but rapid reinfection occurs if there is no reduction in environmental contamination with infective stages, impeding the sustainability of STH control programmes based on deworming alone. WASH for WORMS is a cluster randomised controlled trial assessing the impact of a community-based WASH intervention, implemented by WaterAid Australia, on infection with intestinal parasites following mass albendazole chemotherapy in villages in Timor-Leste. This research will test the hypothesis that a community-based hygiene and sanitation programme will reduce infections of people in communities with gastro-intestinal parasites above that achieved through mass chemotherapy with the benzamidazole anthelminthic drug albendazole. The aims of this study are: 1. To determine the effectiveness of an established community-based hygiene and sanitation programme in reducing the prevalence of parasitic infection (with hookworm, roundworm, whipworm and gastro-intestinal protozoa) following mass albendazole chemotherapy in rural villages in Timor-Leste. 2. To determine the reduction in parasitic disease-related morbidity in children, including anaemia, and stunting and wasting, achieved by implementation of the community-based hygiene and sanitation programme. 3. To evaluate the acceptability and uptake of the community-based hygiene and sanitation programme.
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
49218
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Prof Archie Clements
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Address
49218
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Research School of Population Health
ANU College of Medicine, Biology and Environment
The Australian National University
Building 62 Mills Road
Canberra ACT 0200
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Country
49218
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Australia
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Phone
49218
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+61 2 6125 4578
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Fax
49218
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+61 2 6125 5608
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Email
49218
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[email protected]
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Contact person for public queries
Name
49219
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Susana Nery
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Address
49219
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School of Population Health, University of Queensland
Level 4, Public Health Building;
288 Herston Road; Herston 4006; Queensland
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Country
49219
0
Australia
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Phone
49219
0
+670 7700 5990
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Fax
49219
0
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Email
49219
0
[email protected]
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Contact person for scientific queries
Name
49220
0
Susana Nery
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Address
49220
0
School of Population Health, University of Queensland
Level 4, Public Health Building;
288 Herston Road; Herston 4006; Queensland
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Country
49220
0
Australia
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Phone
49220
0
+670 7700 5990
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Fax
49220
0
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Email
49220
0
[email protected]
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No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
Source
Title
Year of Publication
DOI
Embase
A cluster-randomised controlled trial integrating a community-based water, sanitation and hygiene programme, with mass distribution of albendazole to reduce intestinal parasites in Timor-Leste: The WASH for WORMS research protocol.
2015
https://dx.doi.org/10.1136/bmjopen-2015-009293
Embase
Application of a Multiplex Quantitative PCR to Assess Prevalence and Intensity Of Intestinal Parasite Infections in a Controlled Clinical Trial.
2016
https://dx.doi.org/10.1371/journal.pntd.0004380
Embase
Water, sanitation and hygiene related risk factors for soil-transmitted helminth and Giardia duodenalis infections in rural communities in Timor-Leste.
2016
https://dx.doi.org/10.1016/j.ijpara.2016.07.005
Embase
An environmental assessment and risk map of Ascaris lumbricoides and Necator americanus distributions in Manufahi District, Timor-Leste.
2017
https://dx.doi.org/10.1371/journal.pntd.0005565
Embase
Investigations into the association between soil-transmitted helminth infections, haemoglobin and child development indices in Manufahi District, Timor-Leste.
2017
https://dx.doi.org/10.1186/s13071-017-2084-x
Dimensions AI
A novel, species-specific, real-time PCR assay for the detection of the emerging zoonotic parasite Ancylostoma ceylanicum in human stool
2017
https://doi.org/10.1371/journal.pntd.0005734
Embase
Use of quantitative PCR to assess the efficacy of albendazole against Necator americanus and Ascaris spp. in Manufahi District, Timor-Leste.
2018
https://dx.doi.org/10.1186/s13071-018-2838-0
N.B. These documents automatically identified may not have been verified by the study sponsor.
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