A Pilot Study to Evaluate the Efficacy of Refined Methods to Mitigate Indoor Allergens in North Carolina and Boston, Massachusetts Homes
2 other identifiers
observational
88
1 country
1
Brief Summary
A Pilot Study to Evaluate the Efficacy of Refined Methods to Mitigate Indoor Allergens in North Carolina and Boston, Massachusetts Homes
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Oct 2000
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
October 19, 2000
CompletedFirst Submitted
Initial submission to the registry
June 23, 2006
CompletedFirst Posted
Study publicly available on registry
June 26, 2006
CompletedStudy Completion
Last participant's last visit for all outcomes
September 11, 2006
CompletedJuly 2, 2017
September 11, 2006
June 23, 2006
June 30, 2017
Conditions
Keywords
Eligibility Criteria
You may qualify if:
- To be eligible for the study, each home must:
- have a home occupant who intends to live at the same address for at least 6 months;
- have a home occupant live at the house full time;
- have a home occupant that is at least 21 years of age;
- have at least one bedroom with wall to wall carpeting.
- Yield dust collected during the screening visit that contains combined Der f I plus Der p I allergen levels of greater than or equal to 10 ug/gram dust.
- For the intervention arm only:
- home occupant must have an adult at home during the study visits on weekdays over the six month period that the study is ongoing.
You may not qualify if:
- Indoor Dust Mite Allergen:
- Must have a home occupant who intends to live at the same address for at least 6 months; live at the house full time; be at least 21 years of age; have at least one bedroom with wall to wall carpeting; yield dust collected during the screening visit that contains combined Def fl plus Der pl allergen levels of greater than or equal to 10 ug/gram dust.
- For Intervention arm only - home occupant must have an adult at home during the study visits on weekdays over the six month period that the study is ongoing.
- Indoor Cockroach Allergen:
- Must have a home occupant that intends to live at the same address for at least 6 months; live in the house full time; be at least 21 years of age; have moderate to severe cockroach infestation as evidenced by occupant self-reports of cockroach sightings and by sticky trap assessment that yield a combined total sticky trap count of 50-250 cockroaches.
- For intervention arm only - home occupant must have an adult at home during most of the weekdays over the six month period that the study is ongoing.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
National Institute of Environmental Health Sciences (NIEHS)
Bethesda, Maryland, 20892, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Sponsor Type
- NIH
Study Record Dates
First Submitted
June 23, 2006
First Posted
June 26, 2006
Study Start
October 19, 2000
Study Completion
September 11, 2006
Last Updated
July 2, 2017
Record last verified: 2006-09-11