Identifying Residential Hazards Using Home Test Kits
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|ClinicalTrials.gov Identifier: NCT00285532|
Recruitment Status : Completed
First Posted : February 2, 2006
Last Update Posted : November 18, 2014
|Condition or disease|
A cross-sectional random, stratified study design will be used for this project. All children who are younger than 5 years of age and have a venipuncture blood sample taken at the babies Milk Fund Clinic will be eligible for this study. After checking the lists for errors and duplications, we will randomly permute the sampling frame, stratifying on children's blood lead concentration. Stratification will be used to enroll about 33% of the sample with blood lead concentrations below 5 mg/dl, 33% between 5 to 10 mg/dl, and 33% of 10 mg/dl or higher. Stratifying the sample will improve our chances of testing the predictive validity of home sampling kits to identify children who have blood lead concentration > 10 mg/dl collected by families. In addition this study will:
- Develop a pesticide wipe sampling kit to accompany our lead-sampling kit.
- Evaluate the predictive validity of home sampling kits for lead-contaminated floor dust to identify children who have blood lead levels of 10 mg/dl or higher by community participants compared with repeat samples taken by trained, community workers.
- Evaluate the reliability of home sampling kits for pesticides in dust collected by community participants compared with trained, community workers.
- Disseminate data on the reliability of home sampling tests and provide tools for families to collect environmental samples for large, population-based studies.
- Develop a Healthy Homes Resource Center at the Better Housing League to disseminate information to the community about residential hazards.
|Study Type :||Observational|
|Estimated Enrollment :||150 participants|
|Study Start Date :||October 2001|
|Primary Completion Date :||October 2006|
|Study Completion Date :||October 2006|
|Home test kit|
- Lead and Pesticide Levels [ Time Frame: One time home visit 3-5 days after distribution of kits ]
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00285532
|United States, Ohio|
|University of Cincinnati|
|Cincinnati, Ohio, United States, 45267-0056|
|Principal Investigator:||Sandy M Roda, BS||University of Cincinnati|