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CompletedNCT02373657WUHAUpdated Jun 29, 2021

Water Uptake for Health in Amhara Pilot

An interventional study of instruction in soap-making and hygiene education in Trachoma, sponsored by University of California, San Francisco. Completed at 1 site in Ethiopia. Per ClinicalTrials.gov, last updated 2021-06-29.

Sponsored by University of California, San Francisco · Not applicable, Interventional, and Prevention

Phase
Not applicable
Study type
Interventional
Enrollment
4,068
Allocation
Randomized
Sex
All
01

Study summary

Trachoma is a blinding disease caused by ocular strains of Chlamydia trachomatis. The Carter Center and Proctor Foundation have been jointly conducting trachoma research in the Goncha Siso Enese woreda of Amhara for the past 8 years, through a series of clinical trials. We have found that repeated mass administration of oral azithromycin can greatly reduce the prevalence of trachoma, but mass antibiotics have been unable thus far to eliminate infection. The World Health Organization recommends not only antibiotics for control of trachoma, but an entire SAFE strategy (Surgery for in-turned eyelids, Antibiotics, Facial hygiene promotion, and Environmental improvements such as latrines and water points). Trachoma is more common in villages and households with poor access to water and latrines, so improving the public health infrastructure is thought to be important for limiting transmission of trachoma. However, there is very little evidence to support the efficacy of installing new water points for trachoma. There has been only one previous attempt to study the role of hand dug well installation for trachoma control, and this study, conducted in Niger, found that installing wells was not effective. We now propose a project to improve the public health infrastructure of Goncha Siso Enese woreda by helping with the construction of water points (e.g., hand-dug wells) and providing hygiene education, in order to determine whether improving access to water and hygiene information will be effective for control of trachoma and soil-transmitted helminths.

02

Conditions studied

  • Trachoma

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Keywords

  • trachoma
  • soil transmitted helminths
  • water
  • hand washing
03

In context

Trachoma

39 studies on the registry are indexed under Trachoma; 3 are open to participants now.

This study's enrollment of 4,068 is above the median of 1,300 across 31 interventional studies indexed under Trachoma.

Browse Trachoma studies →

Lead sponsor

University of California, San Francisco is the lead sponsor of 2,169 studies on the registry; 372 are open to participants now.

Of its 267 completed or terminated interventional studies of FDA-regulated products, 202 (76%) have results posted.

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
Yes

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

  • All residents residing in the state-teams which are randomly selected for this study.

Exclusion criteria

Exclusion Criteria:

  • Refusal of village chief (for village inclusion), or refusal of parent or guardian (for individual inclusion)
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
4,068 participants (actual)

Study arms

  • Experimental
    WASH Intervention

    In these seven communities we built a well in a central location for all state team residents. We plan on providing "tippy-taps" (water and soap dispensers), instruction in soap-making, and hygiene education to these communities. We will also put fly traps in the communities to see if wells reduce flies. We plan on performing monitoring visits at 12 months and 24 months, in order to assess clinically active trachoma, ocular chlamydia infection, nasopharyngeal macrolide resistance, soil transmitted helminths, and childhood growth (height and weight). We will also perform assessments of the adequacy of the intervention, by conducting household surveys to assess hygiene behavior, access to water and latrines, and fly density.

    Behavioral: instruction in soap-making and hygiene education

  • No intervention
    Control

    In these seven communities, we plan to perform monitoring visits at 12 months and 24 months, in order to assess clinically active trachoma, ocular chlamydia infection, nasopharyngeal macrolide resistance, soil transmitted helminths, and childhood growth (height and weight). We will also perform assessments of the adequacy of the intervention, by conducting household surveys to assess hygiene behavior, access to water and latrines, and fly density.

Interventions

  • Behavioralinstruction in soap-making and hygiene education
06

What researchers measure

Primary outcomes

  1. Prevalence of ocular chlamydia infection (0-5 year olds)

    Time frame: 24 months

  2. Nasopharyngeal macrolide resistance (0-5 year olds)

    Time frame: 24 months

  3. Prevalence of soil transmitted helminths (Ascaris, Trichuris trichiura, and hookworm) (0-5 year olds)

    Time frame: 24 months

Secondary outcomes

  1. Childhood growth (weight controlled for height among children aged 0-5 years at baseline)

    Time frame: 24 months

  2. Clinically active trachoma in children aged 0-5, as determined by the WHO simplified grading system

    Time frame: 24 months

  3. Prevalence of enteric viruses using PCR (0-5 year olds)

    Time frame: 24 months

  4. Self report childhood morbidity

    Time frame: 24 months

07

Study locations

1 site
  • The Carter Center
    Addis Ababa, Ethiopia
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 29, 2021, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT02373657
Responsible party
Sponsor
First posted
Feb 27, 2015
Start date
Apr 2014
Primary completion
May 2017
Completion
May 2017
Last update
Jun 29, 2021

Study contacts

Jeremy D Keenan, MD, MPH
principal investigator · F.I. Proctor Foundation, University of California San Francisco

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jun 2021. You cannot join it, but the record below documents what was studied.

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