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An Efficacy Trial of a Gravity Fed Household Water Treatment Device as a Delivery System for Zinc

Primary Purpose

Diarrhoea

Status
Completed
Phase
Not Applicable
Locations
Kenya
Study Type
Interventional
Intervention
Zinc enriched water
Sponsored by
Wageningen University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Diarrhoea focused on measuring zinc water diarrhoea growth preschool children

Eligibility Criteria

2 Years - 45 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Children found to have serum zinc concentration <65μg/dL at pre screening.
  • Women that have become pregnant during the study.

Exclusion Criteria for children:

  • Subjects with severe anemia (Hb<7g/dl)
  • Subjects with severe zinc deficiency (SZn<40 μg/dL)
  • Subjects receiving zinc supplementation
  • Subject with chronic diseases affecting zinc metabolism, such as kidney diseases or chronic gastrointestinal disease.
  • Subjects participating in any other clinical trials in the study site

Exclusion criteria for women:

  • Women not residing in the study area until childbirth
  • Subjects with severe anemia (Hb<7g/dl)
  • Subjects with sever zinc deficiency (SZn<40 μg/dL)
  • Subjects receiving zinc supplementation
  • Subject with chronic diseases affecting zinc metabolism, such as kidney diseases or chronic gastrointestinal disease.
  • Subjects currently enrolled in other clinical trials in other trials on the study site

Sites / Locations

  • Maseno University, School of Public health

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

No Intervention

No Intervention

Arm Label

zinc enriched water

purified water only

control group

Arm Description

zinc enriched purified water at 2-6mg/l per day

non zinc enriched, purified drinking water

group of households receiving hygiene practice recommendations and water guard (water purifying solution)

Outcomes

Primary Outcome Measures

zinc status
At baseline, endpoint and at a randomly assigned screening between month 1 and 11, a 6 ml whole blood sample will be collected by venipuncture in 2-5y children (N=270). The blood sample will be used to determine concentration of zinc in the serum (SZn). Inflammation indicator C-reactive protein (CRP) will be analysed to adjust SZn values.

Secondary Outcome Measures

rates of diarrhoea and growth in preschool children

Full Information

First Posted
November 11, 2011
Last Updated
February 27, 2014
Sponsor
Wageningen University
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1. Study Identification

Unique Protocol Identification Number
NCT01481181
Brief Title
An Efficacy Trial of a Gravity Fed Household Water Treatment Device as a Delivery System for Zinc
Official Title
An Efficacy Trial of a Gravity Fed Household Water Treatment Device as a Delivery System for Zinc in Zinc Deficient Children and Women From Low Income Settings
Study Type
Interventional

2. Study Status

Record Verification Date
February 2014
Overall Recruitment Status
Completed
Study Start Date
August 2011 (undefined)
Primary Completion Date
September 2012 (Actual)
Study Completion Date
September 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Wageningen University

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
In low-income settings in developing countries unsafe water is one of the leading causes of high prevalence of waterborne diseases such as diarrhoea.Zinc is an essential trace element that has a critical role in growth and immunity. Supplementation with zinc is considered effective in reducing morbidity from diarrhoeal and other infectious diseases. Verstergaard Frandsen S.A. (Switzerland) has developed a point-of-use water filtration system called LifeStraw®Family (LSF) that removes water's turbidity, reduces the microbiological contamination and enriches water with zinc at a concentration of 3.5 mg/L. The objective of the study is to assess the efficacy of LSF to increase the zinc status (serum zinc concentration) and intake in Kenyan children aged 2-5years with zinc deficiency.The study hypotheses are: A. Use of the LSF device will reduce microbiological contamination of the household supply of drinking and cooking water; B. Use of the LSF device will increase zinc intakes in preschool children; C. Use of the LSF device will increase serum zinc concentration in preschool children; D. Achieving A, B and C will improve growth in preschool children; E. Achieving A, B and C will reduce the frequency and duration of diarrheal disease in preschool children and in members of the participating households.
Detailed Description
Introduction: In low-income settings in developing countries unsafe water is one of the leading causes of high prevalence of waterborne diseases such as diarrhoea. Point-of-use water treatment systems are currently considered by UNICEF as more effective in delivering safe drinking water than interventions applied at source. Zinc is an essential trace element that has a critical role in growth and immunity. Supplementation with zinc is considered effective in reducing morbidity from diarrhoeal and other infectious diseases. Verstergaard Frandsen S.A. (Switzerland) has developed a point-of-use water filtration system called LifeStraw®Family (LSF) that removes water's turbidity, reduces the microbiological contamination and enriches water with zinc at a concentration of 3.5 mg/L. Objective: To assess the efficacy of LSF to increase the zinc status (serum zinc concentration) and intake in Kenyan children aged 2-5years with zinc deficiency. Study Design and Methods: A study population living in an area with low Zn status and sharing the same unimproved water supply will be included in the trial and randomly assigned to one of the treatment groups for 12 months. All households will receive hygiene practice recommendations (HPRs). In addition to HPR, group one will receive the LSF device with the zinc delivery system; group 2 will receive HPRs and a LSF without zinc delivery system, and group 3 will receive HPRs. At baseline, mid-point and end-point, anthropometrics (weight, height, mid-upper arm circumference MUAC), and 7 ml whole blood will be collected from preschool children for determination of SZn, C-reactive protein (CRP), hemoglobin (Hb) and serum ferritin (SF). Children and adult subjects remaining zinc deficient at completion of the trial will receive zinc supplements. Expected outcome: This study will investigate the efficacy of a water treatment device as a means to provide Zn in communities where high prevalence of surface water use and zinc deficiency coexists. Increasing the microbiological quality of water and the contemporaneous low dose fortification with zinc, could prove useful in the global effort to control zinc deficiency and increase the supply of clean drinking water

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diarrhoea
Keywords
zinc water diarrhoea growth preschool children

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
270 (Actual)

8. Arms, Groups, and Interventions

Arm Title
zinc enriched water
Arm Type
Experimental
Arm Description
zinc enriched purified water at 2-6mg/l per day
Arm Title
purified water only
Arm Type
No Intervention
Arm Description
non zinc enriched, purified drinking water
Arm Title
control group
Arm Type
No Intervention
Arm Description
group of households receiving hygiene practice recommendations and water guard (water purifying solution)
Intervention Type
Dietary Supplement
Intervention Name(s)
Zinc enriched water
Intervention Description
3mg zinc/L of purified water from a filter installed in the households
Primary Outcome Measure Information:
Title
zinc status
Description
At baseline, endpoint and at a randomly assigned screening between month 1 and 11, a 6 ml whole blood sample will be collected by venipuncture in 2-5y children (N=270). The blood sample will be used to determine concentration of zinc in the serum (SZn). Inflammation indicator C-reactive protein (CRP) will be analysed to adjust SZn values.
Time Frame
one year
Secondary Outcome Measure Information:
Title
rates of diarrhoea and growth in preschool children
Time Frame
one year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
2 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Children found to have serum zinc concentration <65μg/dL at pre screening. Women that have become pregnant during the study. Exclusion Criteria for children: Subjects with severe anemia (Hb<7g/dl) Subjects with severe zinc deficiency (SZn<40 μg/dL) Subjects receiving zinc supplementation Subject with chronic diseases affecting zinc metabolism, such as kidney diseases or chronic gastrointestinal disease. Subjects participating in any other clinical trials in the study site Exclusion criteria for women: Women not residing in the study area until childbirth Subjects with severe anemia (Hb<7g/dl) Subjects with sever zinc deficiency (SZn<40 μg/dL) Subjects receiving zinc supplementation Subject with chronic diseases affecting zinc metabolism, such as kidney diseases or chronic gastrointestinal disease. Subjects currently enrolled in other clinical trials in other trials on the study site
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michael Zimmerman, MD, PhD
Organizational Affiliation
ETH Zurich , Wageningen University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Diego Moretti, PhD
Organizational Affiliation
Wageningen University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Maseno University, School of Public health
City
Kisumu
State/Province
Western Kenya
ZIP/Postal Code
+254
Country
Kenya

12. IPD Sharing Statement

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An Efficacy Trial of a Gravity Fed Household Water Treatment Device as a Delivery System for Zinc

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