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CompletedNCT05914363SABABUUpdated Jan 30, 2025

Evaluating Impact of Improved Floors on Health

An interventional study of Sealed washable floor plus behaviour change and Behaviour change intervention in Diarrhoeal Disease, Hookworm Infection and Ascaris Lumbricoides Infection, sponsored by London School of Hygiene and Tropical Medicine. Completed at 1 site in Kenya. Per ClinicalTrials.gov, last updated 2025-01-30.

Sponsored by London School of Hygiene and Tropical Medicine · Not applicable, Interventional, and Prevention

Phase
Not applicable
Study type
Interventional
Enrollment
2,200
Allocation
Randomized
Sex
All
01

Study summary

The goal of this intervention study is to learn about the impact of household flooring on health in rural Kenya, and test whether providing an improved (cement stabilised, washable) floor improves the health of children and their care providers.

The main questions the study aims to answer are:

  • What is the effect of providing a sealed, washable floor on the prevalence of infections that cause diarrhoea, intestinal worms and sand flea infections?
  • To what extent does the intervention reduce contamination of floors with pathogens within the home?
  • What is its effect of the intervention on the wellbeing of caregivers and children?
  • Over the course of a year, do the new floors remain undamaged, with no cracks?
  • Do participants living with the new floors, and the masons that helped to install the floors, like them and feel they are practical and affordable?

The study will involve a trial, where half of the recruited households will be randomly chosen to receive the new floor in addition to some support on how to care for the floor and keep it clean. The other half of households will not receive anything at first, but at the end of the research project will also receive a new floor.

Before the new floors are installed, the investigators will make several assessments in all study households. These will include a survey to measure household characteristics; a stool survey, to measure how many people are infected with diarrhoea-causing microorganisms and parasitic worms; a jigger flea examination among children; wellbeing assessments among children and caregivers; and soil sampling to identify microorganisms on the floor of the household.

When households receive the new floor, participants will have to move out of their house for up to 7 days during installation. Participants will also be asked to attend some group meetings to discuss ways of taking care of the floor and keeping it clean.

Assessments will be repeated 12 months after the floor has been delivered, and additional interviews will be held with a small number of randomly selected participants. Throughout the 12 months following delivery of the intervention, investigators will make unannounced visits to households to check the condition of the floor. Participants will also be offered treatment for parasitic worm infections after assessments have been completed at the start and end of the project.

Read the detailed description

Earthen floors are often damp or dusty and difficult to clean, providing an ideal environment for faecal pathogens and parasites. Cross-sectional studies have revealed associations between household flooring and health outcomes, but robust experimental evidence is scant. This study will evaluate the impact of an improved household flooring intervention on enteric infections, soil-transmitted helminth (STH) infections, and tungiasis through implementation of a cluster-randomised trial in two rural settings in Kwale and Bungoma Counties, Kenya.

The primary aim of this study is to evaluate the effectiveness of an improved flooring intervention in reducing the burden of enteric infections, STH and tungiasis in participating households through implementation of a randomised controlled trial (RCT) in two distinct settings in rural Kenya. The primary objectives are to quantify impact on the prevalence of enteric infections, STH infections, and tungiasis. Secondary objectives include assessing impact on the wellbeing of caregivers and children, self-report gastrointestinal illness in children, and the extent to which entero-pathogen and parasitic contamination of floors is reduced within the home. We will also examine the differential effects across community and household contexts (including water, sanitation, and hygiene (WASH) infrastructure, animal husbandry, user adherence and study site). Lastly, we deliver a process evaluation to determine the practicality, acceptability, costs, and durability of the improved flooring intervention and how environmental, installation, and use factors affect these.

In total, 440 clusters (households) across both sites are allocated to either control or intervention group, in which a low-cost, sealed, washable cement-based floor is installed in all eligible buildings of the dwelling, alongside a floor care guide provided during an induction meeting. Prevalence of enteric infections in children under 5 years will be assessed via stool surveys and PCR; prevalence of tungiasis infection in children 1-14 years based on clinical exam; and prevalence of STH infection in all household members over 1 year assessed via Kato-Katz. Following the 12-month implementation period and final assessments, control households will be offered improved floors.

02

Conditions studied

  • Diarrhoeal Disease
  • Hookworm Infection
  • Ascaris Lumbricoides Infection
  • Trichuris Infection
  • Tungiasis
03

In context

Hookworm Infections

39 studies on the registry are indexed under Hookworm Infections; 5 are open to participants now.

This study's enrollment of 2,200 is above the median of 182 across 36 interventional studies indexed under Hookworm Infections.

Browse Hookworm Infections studies →

Lead sponsor

London School of Hygiene and Tropical Medicine is the lead sponsor of 298 studies on the registry; 15 are 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
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

  • Household with a child under 5 years of age that meets structural criteria (unimproved earthen flooring throughout, structurally sound), with members willing to temporarily relocate.

Exclusion criteria

Exclusion Criteria:

  • Households that are intending to move within the next 12 months, or that have improved flooring in any rooms or are not structurally sound.
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
2,200 participants (actual)

Study arms

  • Experimental
    Intervention (improved floor)

    * Replacement of rudimentary floors with an improved floor, * Support for behaviour change through 'floor clubs'. * Annual mass treatment for STH infections (400 mg albendazole) * Treatment of tungiasis in those affected by heavy infections (at 0 and 12 months) according to county DoH recommendations

    Other: Sealed washable floor plus behaviour change · Behavioral: Behaviour change intervention · Drug: Routine deworming · Procedure: treatment for tungiasis

  • Active comparator
    Control (rudimental floor)

    * Annual mass treatment for STH infections (400 mg albendazole) * Treatment of tungiasis in those affected by heavy infections (at 0 and 12 months) according to county DoH recommendations

    Drug: Routine deworming · Procedure: treatment for tungiasis

Interventions

  • OtherSealed washable floor plus behaviour change

    Replacement of rudimentary floors with a cement stabilised floor in all rooms in the dwelling

  • BehavioralBehaviour change intervention

    Support for behaviour change through 'floor clubs' and the provision of printed guides

  • Treatment of all household members for STH infections (400 mg albendazole in those aged 24 months and above; 200 mg albendazole in those aged 12-23 months)

    Also known as: albendazole

  • Proceduretreatment for tungiasis

    Treatment of tungiasis in those affected by heavy infections (at 0 and 12 months) according to county Department of Health recommendations

06

What researchers measure

Primary outcomes

  1. Enteric infections

    Prevalence of enteric infections (detected through PCR) in children under 5 years old will be assessed using cross-sectional stool surveys including all enrolled children under 5 years before installation of floors and 12 months after receiving the floors. Pathogens to be identified from those observed at baseline using a multipathogen panel on a subset of 100 samples.

    Time frame: 12 months

  2. Tungiasis infections

    Prevalence of tungiasis (detected through clinical examination of hands and feet) in children under 15 years old will be assessed using cross-sectional clinical assessment surveys including all enrolled children under 15 years before installation of floors and 12 months after receiving the floors.

    Time frame: 12 months

  3. STH infections

    Prevalence of at least one STH infection (hookworm, ascaris and trichuris infections; detected through kato katz) in all household members 12 months and older will be assessed using cross-sectional stool surveys including all enrolled people over 12 months of age before installation of floors and 12 months after receiving the floors.

    Time frame: 12 months

Secondary outcomes

  1. Gastrointestinal illness

    Prevalence of gastrointestinal illness in children under 5 years - assessed in both study arms based on caregiver reported symptoms

    Time frame: 12 months

  2. Intensity and severity of tungiasis

    Intensity of tungiasis and severity of acute and chronic tungiasis-associated pathology in children \<15 years - assessed using clinical severity scores (range: 0-110, high scores indicating increased severity/worse outcome)

    Time frame: 12 months

  3. Quality of Life for children aged 8 to 14 years

    Quality of Life assessed in children ages 8 to 14 years in both arms using the standardised EQ5D-Y (EuroQol 5-dimension health-related quality of life tool for children; values are anchored at 1 (full health) and 0 (a state as bad as being dead))

    Time frame: 12 months

  4. Quality of Life and subjective wellbeing in primary caregivers

    Quality of Life assessed in primary caregivers in both arms using the standardised EQ5D tool (EuroQol 5-dimension health-related quality of life tool for adults; values are anchored at 1 (full health) and 0 (a state as bad as being dead))

    Time frame: 12 months

  5. Prevalence of Ascaris lumbricoides infection

    Ascaris lumbricoides (roundworm) infection prevalence in all household members \>1 year assessed using Kato Katz

    Time frame: 12 months

  6. Prevalence of hookworm infection

    Hookworm infection prevalence in all household members \>1 year assessed using Kato Katz

    Time frame: 12 months

  7. Prevalence of Trichuris trichiura infection

    T. trichiura (whipworm) infection prevalence in all household members \>1 year assessed using Kato Katz

    Time frame: 12 months

  8. Environmental contamination - enteric pathogens

    Environmental contamination for human-specific and animal faecal markers - assessed from dust/soil samples from household cooking areas and living rooms using PCR.

    Time frame: 12 months

  9. Environmental contamination - tungiasis

    Contamination of floors with eggs, larvae, pupae and adults of T. penetrans - assessed through entomology soil surveys

    Time frame: 6 months

07

Study locations

1 site
  • Dzombo ward
    Kwale, Kenya
08

References and documents

Individual participant data

Plan to share: Yes — Data collected from this study and underlying each article (text, tables, figures, and appendices), including quantitative, de-identified, individual participant data and a data dictionary, will be made available following publication of the article(s).

Supporting information: Study protocol, Statistical analysis plan, Informed consent form, Clinical study report

Time frame: The quantitative, individual, de-identified, participant data that underlie the results reported in each published article (text, tables, figures, and appendices) will be made available within three months of publication of each article, with no end date.

Access criteria: The data will be made available to members of the scientific and medical community for non-commercial use only, upon email request to the corresponding author. Written proposals will be assessed by members of the SABABU Trial Group and a decision made about the appropriateness of the use of data. Data will be stored at LSHTM Data Compass, the London School of Hygiene \& Tropical Medicine digital data repository The data will be available to anyone who wishes to access the data through the LSHTM Data Compass, the London School of Hygiene \& Tropical Medicine digital data repository. URL is https://datacompass.lshtm.ac.uk/

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 30, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05914363
Collaborators
Kenya Medical Research Institute, Jomo Kenyatta University of Agriculture and Technology, International Centre of Insect Physiology and Ecology (ICIPE)
Responsible party
Sponsor
First posted
Jun 22, 2023
Start date
Apr 12, 2023
Primary completion
Aug 31, 2024
Completion
Sep 30, 2024
Last update
Jan 30, 2025

Study contacts

Rachel Pullan, PhD
principal investigator · London School of Hygiene and Tropical Medicine
Ulrike Fillinger, PhD
principal investigator · icipe
Charles Mwandawiro, PhD
principal investigator · Kenya Medical Research Institute
James Wambua KALULI, PhD
principal investigator · JKUAT

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Jun 2024. You cannot join it, but the record below documents what was studied.

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