Lead Exposure Registry of Flint Residents (Michigan)

 
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    CFDA#

    93.197
     

    Funder Type

    Federal Government

    IT Classification

    B - Readily funds technology as part of an award

    Authority

    Department of Health and Human Services (HHS)

    Summary

    During April 25, 2014–October 15, 2015, approximately 99,000 residents of the City of Flint, MI, were exposed to lead when the water source was switched from the Detroit Water Authority to the FWS. The Centers for Disease Control and Prevention (CDC) announces the availability of FY2017 funds to support the City of Flint, Michigan, and the State of Michigan to build their capacity to: 1) identify communication and training strategies for a registry of residents exposed to lead-contaminated water from the Flint River during April 25, 2014– October 15, 2015; 2) develop the registry to identify eligible residents; 3) recruit and enroll eligible residents, collect their baseline information, and refer them to services; 4) ensure a referral process to link registrants to comprehensive, coordinated services to mitigate the effects of lead exposure; and 5) select appropriate measures and frequency of follow-up to collect data on exposure, health, and developmental milestones along with choices of interventions, services, and enrichment activities undertaken during the 4 year project period
     
    This program supports the following strategies and activities:
    • Strategy 1 - Identify communication and training strategies for a registry of residents exposed to lead-contaminated water from the FWS during April 25, 2014–October 15, 2015.
    • Strategy 2 - Develop the registry to identify eligible residents.
    • Strategy 3 - Recruit and enroll eligible residents, collect their baseline information, and refer them to services.
    • Strategy 4 - Ensure a referral process to link registrants to comprehensive, coordinated services to mitigate the effects of lead exposure.
    • Strategy 5 - Select appropriate measures and frequency of follow-up to collect data on exposure, health, and developmental milestones along with choices of interventions, services, and enrichment activities undertaken during the project period.
     

    History of Funding

    None is available.

    Additional Information

    Short-Term Outcomes
    Community and Providers have:
    • Increased awareness of registry goals and scope
    • Increased awareness of eligibility criteria for registry
    Community, Providers, and Workforce have increased knowledge of:
    • Adverse health and developmental outcomes from lead exposure
    • Blood lead testing and reporting requirements
    • Medical management recommendations
    • Environmental lead exposure sources and reduction methods
    • Modifiable factors for lead exposure reduction
    • Available preventive referral services and interventions to reduce the impact of lead exposure
    Registry Protocol enables metrics for:
    • Increased registrant referral to services over baseline
    • Target number of registry follow-ups achieved per registrant
    Intermediate Outcomes
    Registrants:
    • Use preventive services
    • Reduce environmental lead exposures where they live, work, and play
    • Have lower blood lead levels
    • Have better health and fewer developmental delays
    Registry data collection leads to:
    • Increased quality and quantity of data to inform lead poisoning prevention policy and program administration
    • Increased knowledge about the effectiveness of the number of prevention services leading to improved outcomes
    • Increased knowledge about the effectiveness of different types of prevention services leading to improved outcomes
    • Increased knowledge about acute and long-term impacts of lead exposure
    Michigan State University (MSU) is already building a registry to support Flint residents. In January of 2017, the Michigan Department of Health and Human Services awarded a one-year grant of $500,000 to MSU College of Human Medicine for the planning of a registry for Flint residents. MSU's plan to build a registry is divided into two phases:
    • Phase I of registry planning: clarify registry scope, definition(s), goals and objectives, stakeholders/partners, advisory structure, priorities (by tier) and deliverables.
    • Phase II of registry planning: identify and begin to develop infrastructure required for the registry as well as the case management/resource linkages; develop processes for linkage of pre-existing cohorts and environmental data sets; develop guidelines for how registry data will be protected and utilized once operationalized; and develop process for ongoing registry operation and maintenance.

    Contacts

    Stephanie Davis

    Stephanie Davis
    Centers for Disease Control and Prevention
    1600 Clifton Road
    Atlanta, GA 30329-4027
    (770) 488-3676
     

  • Eligibility Details

    This is a single source eligibility program. Funding is limited to Michigan State University.

    Deadline Details

    Applications are to be submitted by June 28, 2017.

    Award Details

    Approximately $14,400,000 is available in total funding. One award will be granted. Award ranges from $1,200,000 to $6,000,000 per year. Average yearly award is $3,600,000. Project length is four years. Cost sharing or matching funds are not required for this program.

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