- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00839046
A Community-based Participatory Research (CBPR) Intervention for Childhood Asthma Using Air Filters and Air Conditioners (CAAA)
July 20, 2017 updated by: Toby Lewis, University of Michigan
A Community Based Participatory Research Intervention for Childhood Asthma Using Air Filters and Air Conditioners
The burden of childhood asthma is borne disproportionately by children living in poverty and in urban centers, many of whom are from communities of color and are at greater risk for environmental exposures.
Given the complex interaction of physical and social environmental factors on childhood asthma, there have been increasing calls for comprehensive efforts using a community-based participatory research (CBPR) approach.
Community Action Against Asthma is a long standing CBPR partnership in Detroit, Michigan, composed of representatives from community-based organizations, health and human service agencies, and academia.
All members of the partnership have been actively involved in the development of the CBPR project proposed here.
The specific aims are: 1) to test the efficacy of air filters (AFs) separately and when combined with air conditioners (ACs) to reduce exposure to particulate matter (PM), over and above a standard community health worker home visit (standard) intervention; 2) to test the association between any reduction in PM exposure through the use of AFs separately and when combined with ACs over and above a standard intervention and health outcomes in children with asthma; 3) to elucidate the causal pathways by which any intervention-related improvements in children's asthma-related health status is occurring.
One hundred and fifty households in Detroit, Michigan with at least one child with mild persistent or moderate to severe persistent asthma will be enrolled to participate in the study.
Households will be randomly assigned to one of three groups: a standard household intervention (or control) group; an AF only intervention group; or an AF+AC intervention group.
Extensive health and exposure measures will be undertaken during the course of the 12 -month intervention.
Given the role of PM in children's asthma-related health and the higher concentrations of PM in microenvironments, there is a need to test the efficacy and efficiency of novel approaches to reducing indoor air pollutants.
Doing so using a CBPR approach will enhance the relevance and ultimately the success of this proposed research.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
For the proposed study we will conduct a randomized controlled trial (RCT) comparing a standard community health worker home visit intervention (the standard intervention) to an Air Filter(AF) only intervention that adds the use of an AF in the child's bedroom to the standard intervention (AF only intervention) and an Air Filter(AF)+ Air Conditioner (AC) intervention that adds the use of an AF and AC in the child's bedroom to the standard intervention (AF+AC intervention) (Figure 1).
We will test whether the addition of AFs (and, in the warmer months, ACs) to the standard intervention, as compared to the standard intervention will: (1) further lower children's exposure to PM (Specific Aims 1a, 1b), and (2) further improve asthma-related health status of children (Aims 2a, 2b).
One hundred and fifty Detroit households with at least one child aged 6 to 12 with symptoms consistent with persistent asthma (mild, moderate, or severe) will be enrolled in the study .
Following collection of baseline data, households will be randomly assigned to receive one of three interventions: the standard household intervention, the AF only intervention, or the AF+AC intervention.
Participants assigned to the AF only intervention group will receive AFs at the start of the 12-month intervention (Summer/Fall 2008).
Those assigned to the AF+AC intervention group will receive AFs at the start of the intervention period but ACs will not be in place during the first summer of the intervention, but will be installed in June 2009 prior to the second summer of the intervention (Figure 2).
Data will be collected across all seasons (Fall 2008 through Winter 2009) which will enable us to evaluate directly the exposure and health outcome effects (Specific Aims 1a and 2a, respectively) of the addition of AFs alone to the standard intervention as well as the exposure and health outcome effects of the AFs augmented by ACs (Aims 1b, 2b).
This design will also allow for comparisons, adjusted for any changes in the exposure and health status of the intervention groups, of the combined effect of the AC and AF to that of the AF alone.
Study Type
Interventional
Enrollment (Actual)
126
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Michigan
-
Ann Arbor, Michigan, United States, 48109-2029
- University of Michigan
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
6 years to 12 years (Child)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Residents of EastSide or Southwest Detroit
- child in the family between age of 6-12 with responses to the screening questionnaire consistent with known or probable persistent (mild, moderate, or severe) asthma
Exclusion Criteria
- the family participated in our previous intervention study in Detroit
- the family experiences continuous homelessness during the period of enrollment;
- the child spends fewer than 80% of nights at the primary household during the school year
- the child has a physical or mental handicap that would preclude successful completion of the child survey and spirometry.
- the child spends fewer than 28 consecutive nights (4 weeks) during the summer (i.e., June, July, and August) at the primary household
- the family is monolingual in a language other than English or Spanish;
- the electrical wiring of the house is inadequate for use of the air filter/air conditioner (AF/AC)
- the home lacks a closable door to the room where the child usually sleeps
- there is already an existent window AC unit in the room where the child usually sleeps
- the window in the room where the child usually sleeps will not support the addition of a window AC unit.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: 1 Community Health Worker Intervention
This is the active control group, which all 150 participants will receive.
It consists of visits from trained community health workers, who will provide asthma education, as well as provision of equipment and supplies to reduce indoor environmental exposures for asthma.
These will include: vacuum cleaners, mattress and pillow covers, cleaning supplies.
|
The Community Health Worker (CHW) intervention consists of visits by CHWS to help families reduce children's exposure to common asthma triggers (allergens and irritants) in the indoor environment.
The content of the CHW visits and the materials distributed will follow NHLBI Expert Panel Report 2 recommendations.
Each household will receive 6 visits over a 12-month period in which the CHW will provide education on environmental triggers (e.g., reduction of dust mites, cockroaches, cat and dog dander, and environmental tobacco smoke); materials including vacuum cleaners with HEPA filters, mattress and pillow covers, and cleaning supplies; social support to the caregivers; and, if indicated, referrals to other services.
Other Names:
|
|
Experimental: 2 Air Filter
The 50 families in the Air Filter Arm will receive an air filter in addition to the standard community health worker intervention.
The Air Filter will be installed right after baseline measurements in the home.
|
Fifty households will receive an Air Filter, in addition to receiving the standard community health worker intervention.
These households will receive a HEPA room AF (Whirlpool 510 or equivalent), a relatively high capacity unit that can be quietly operated.
Similar to other studies the filter will be placed in the room where the child sleeps.
The HEPA AF will be installed at the beginning of the intervention period.
|
|
Experimental: 3 Air Filter and Air Conditioner
Fifty families will be assigned to the "Air Filter and Air Conditioner" Arm.
In addition to the standard community health worker intervention, they will receive an air filter and an air conditioner (for the warmer months).
|
Fifty households will receive the air filter and the air conditioner, in addition to receiving the standard community health worker intervention.
The air filter will be installed at the beginning of the intervention, after baseline measurement.
In the spring of the year (2009), a small window AC unit (Whirlpool Designer Style ACQ058MM or equivalent) will also be installed in the room where the child sleeps.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Improved Lung Function in Children with Asthma
Time Frame: End of one year of intervention
|
End of one year of intervention
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Reduced Particulate Matter (PM) in the home of the children with asthma
Time Frame: End of one year intervention
|
End of one year intervention
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Toby C Lewis, MD, University of Michigan School of Public Health
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
August 1, 2007
Primary Completion (Actual)
October 1, 2010
Study Completion (Actual)
October 1, 2010
Study Registration Dates
First Submitted
February 5, 2009
First Submitted That Met QC Criteria
February 6, 2009
First Posted (Estimate)
February 9, 2009
Study Record Updates
Last Update Posted (Actual)
July 24, 2017
Last Update Submitted That Met QC Criteria
July 20, 2017
Last Verified
July 1, 2017
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- R01ES014566 (U.S. NIH Grant/Contract)
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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