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Completed

NCT Number: NCT02613585

Tick-borne Illness and Clothing Study of Rhode Island

Lyme and other tick-borne diseases pose a significant health threat to outdoor workers. This study is a double-blind randomized controlled trial of outdoor workers in Rhode Island and the surrounding area that will address the following study aims: 1) Evaluate the effectiveness of LLPI clothing in preventing tick bites among outdoor workers in Lyme endemic areas; 2) Measure the urine levels of permethrin metabolites in study subjects; and 3) Measure the loss over time of knockdown activity against ticks and of permethrin in LLPI clothing.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Rhode Island

Kingston, Rhode Island, 02881, United States

About this study

Lyme and other tick-borne diseases pose a significant health threat to outdoor workers. In a double-blind randomized controlled trial (RCT) in North Carolina outdoor workers, the investigators previously showed that long-lasting permethrin-impregnated (LLPI) clothing provided >80% protection for one year against Lone Star tick bites among outdoor workers in North Carolina. But there are three issues that need to be addressed before this finding can be translated into policy: 1) Do LLPI clothing protect against black legged ticks, the vector for Lyme disease, babesiosis and anaplasmosis? 2) What levels of permethrin and its metabolites are absorbed, and are they potentially toxic? 3) Why did the LLPI clothing in our previous study lose efficacy after a year?

Participants: The investigators will recruit 250 outdoor workers. The investigators anticipate recruiting 80, 80, 40,30, and 20 participants from NationalGrid, the RI Department of Environmental Management, the Massachusetts Department of Conservation & Recreation, the National Park Service, and the US Fish & Wildlife Service.

Procedures (methods): This will be a randomized controlled trial. All study subjects will fill out weekly tick logs, collect attached ticks for later speciation and pathogen detection, and submit annual serum samples to test for exposure to tick-borne pathogens. A randomly selected subset of 60 subjects also will be asked to submit urine samples for permethrin metabolite analysis at several time points during follow-up. An additional randomly selected subset (n=30) will be asked to submit worn items of clothing for tick knockdown testing and permethrin content analysis at the end of the first and second years of field testing.

The results of this study could help protect hundreds of thousands of outdoor workers with exposure to ticks and tick-borne pathogens.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • over 18 years of age,
  • spending an average of 10 or more hours of outdoor work per week during peak tick season, and
  • completion of written informed consent.

Exclusion criteria

  • pregnancy or a planned pregnancy during the follow-up period (since exposure to an insecticide is involved),
  • non-English speakers, or
  • having a known allergy or sensitivity to insecticides

Treatment and study plan

Permethrin Impregnated Clothing

Other

Uniforms and work clothing treated with permethrin according to proprietary process used by Insect Shield, Inc.

Other names: Insect Shield

Primary outcomes

  1. Number of Work Related Tick Bites Per Week

    Time frame: Weekly for two years

    Reported tick bites, defined as ticks attached to or embedded in the skin.

Secondary outcomes

  1. Change in permethrin metabolite levels after 3 weeks

    Time frame: Enrollment to 3 weeks after study initiation

    Permethrin metabolites measured in urine, compared to baseline prior to wearing clothing.

  2. Change in permethrin metabolite levels after 1 year

    Time frame: Enrollment to end of study year 1

    Metabolites measured in urine, compared to baseline prior to wearing clothing.

  3. Change in concentration of permethrin in clothing after 1 year

    Time frame: Enrollment to end of study year 1

    Measurement of the chemical concentration of clothing samples after study year 1, compared against concentration of a newly treated clothing sample.

  4. Change in concentration of permethrin in clothing after 2 years

    Time frame: Enrollment to 2 years after study initiation

    Measurement of the chemical concentration of clothing samples after study year 2, compared against concentration of a newly treated clothing sample.

  5. Change in tick repellency after 1 year

    Time frame: Enrollment to 1 year after study initiation

    Measurement of the tick repellency ("knockdown activity") of clothing samples after study year 1, compared against concentration of a newly treated piece of clothing sample.

  6. Change in tick repellency after 2 years

    Time frame: Enrollment to 2 years after study initiation

    Measurement of the tick repellency ("knockdown activity") of clothing samples after study year 2, compared against concentration of a newly treated piece of clothing sample.

  7. Pathogen seroconversion in study year 1

    Time frame: Enrollment to year 1

    Seroconversion in year 1 is defined as a fourfold rise in antibody titers against pathogens of tick-borne disease when comparing titers between baseline and after year 1.

  8. Pathogen seroconversion in study year 2

    Time frame: Study year 1 to study year 2

    Seroconversion in year 2 is defined as a fourfold rise in antibody titers against pathogens of tick-borne disease when comparing titers between baseline and after year 2.

Sponsors and collaborators

Lead sponsor

University of North Carolina, Chapel Hill

Other

Collaborators

  • East Carolina University
  • National Institute for Occupational Safety and Health (NIOSH/CDC)
  • University of Rhode Island

Registry information

Important dates

Study start
2016
Primary completion
2019
Study completion
2020
First posted
Nov 24, 2015
Registry last updated
Mar 10, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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