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Mapping Snakebite Risk in Kenya and Eswatini

NCT06124872 · Status: ENROLLING_BY_INVITATION · Type: OBSERVATIONAL · Enrollment: 70000

Last updated 2023-11-09

No results posted yet for this study

Summary

The goal of this observational study is to learn about how snakebite risk varies in different environments in Kenya and understand how this information can be used to support decision makers.

The main questions it aims to answer are:

1. To what extent can information on snakebite cases and data on geographic, climatic and sociodemographic factors be used to predict geographical variation in snakebite risk in Kenya and Eswatini?
2. What is the most effective means of presenting outputs from spatial analysis of snakebite risk to ensure its effective use in research and healthcare decision making?

Participants in the community survey will be asked survey questions about the history of snakebite in their household. Participants in the key informant interviews will be interviewed to understand how data on snakebite risk can be best presented to support their work.

Conditions

  • Snakebite
  • Epidemiology

Interventions

OTHER

Survey questionnaire

Household screening questionnaire Snakebite details questionnaire where a history of snakebite is reported

OTHER

Key informant interview

Semi-structured interview with selected key informants

Sponsors & Collaborators

  • Kenya Medical Research Institute

    collaborator OTHER

  • Institute of Primate Research

    collaborator OTHER_GOV

  • Liverpool School of Tropical Medicine

    lead OTHER

Principal Investigators

  • Collinson · Liverpool School of Tropical Medicine

Eligibility

Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2023-06-01
Primary Completion
2024-12-31
Completion
2024-12-31

Countries

  • Kenya

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06124872 on ClinicalTrials.gov