Opportunity Information: Apply for RFA DP 15 009

  • The Centers for Disease Control and Prevention in the health sector is offering a public funding opportunity titled "Improving Surveillance and Prevention of Epilepsy Burden in US Communities" and is now available to receive applicants.
  • Interested and eligible applicants and submit their applications by referencing the CFDA number(s): 93.068 Chronic Diseases Research, Control, and Prevention.
  • This funding opportunity was created on Feb 17, 2015 and posted on Dec 23, 2014.
  • Applicants must submit their applications by Feb 26, 2015 Letter of Intent Due Date 01/26/2015Application Due Date 02/26/2015 BY 5PM EST. (Agency may still review applications by suitable applicants for the remaining/unused allocated funding in 2026.)
  • The funding agency has allocated a total of $1,800,000.00 to eligible and selected applicants.
  • Each selected applicant is eligible to receive up to $300,000.00 in funding.
  • The number of recipients for this funding is limited to 2 candidate(s).
  • Eligible applicants include: Others (see text field entitled Additional Information on Eligibility for clarification).
  • Hispanic serving Institutions Historically Black Colleges and Universities (HBCUs) Tribally Controlled Colleges and Universities (TCCUs) Alaska Native and Native Hawaiian Serving Institutions Eligible Agencies of the Federal Government U.S. Territory or Possession Faith based or Community based Organizations Regional Organizations Bona Fide Agents Federally Funded Research and Development Centers (FFRDCs)
Apply for RFA DP 15 009

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Opportunity Summary:

The grant opportunity "Improving Surveillance and Prevention of Epilepsy Burden in US Communities" (Funding Opportunity Number RFA DP 15 009) was a CDC discretionary funding announcement offering support through a cooperative agreement mechanism. Its central aim was to strengthen epilepsy public health surveillance by applying standardized definitions and consistent methods so that estimates and findings are comparable across communities and over time. In practical terms, the CDC was seeking projects that could generate clearer, more reliable information about how many people have epilepsy (prevalence) and/or how many new cases occur over a given period (incidence), especially within specific U.S. populations and subpopulations where the burden may be undermeasured or unevenly distributed.

A major emphasis of the announcement was addressing health disparities. The CDC framed the work as more than counting cases; applicants were expected to use surveillance-quality data to expand knowledge about determinants of epilepsy outcomes. That includes identifying risk factors and other influences that shape epilepsy incidence, prevalence, and related outcomes in real-world settings. The intent was that stronger evidence on who is affected, where, and why would directly inform better-targeted interventions and services. Those interventions could span prevention, treatment support, and rehabilitation, with the broader public health goal of reducing inequities and minimizing the disproportionate impact of epilepsy on certain communities.

Because the award type was a cooperative agreement, the CDC would typically expect substantial involvement in the project beyond issuing funds, such as collaboration on methods, measures, or dissemination strategies. The announcement sat in the health activity category and was tied to CFDA 93.068 (Chronic Diseases Research, Control, and Prevention). There was no cost sharing or matching requirement, lowering the barrier for organizations that might otherwise struggle to provide non-federal funds.

Funding details indicate an estimated total of $1,800,000 with an award ceiling of $300,000 and an award floor listed as $0, and the CDC anticipated making two awards. The posting date was December 23, 2014, with key deadlines of a Letter of Intent due January 26, 2015, and a full application due February 26, 2015 by 5:00 PM Eastern. The opportunity later moved to archive status on March 28, 2015, indicating it was no longer accepting applications after that cycle.

Eligibility was broad and intentionally inclusive of institutions and organizations positioned to work with underserved or priority populations. Eligible applicants included Hispanic-serving Institutions, Historically Black Colleges and Universities, Tribally Controlled Colleges and Universities, Alaska Native and Native Hawaiian Serving Institutions, eligible federal agencies, U.S. territories or possessions, faith-based and community-based organizations, regional organizations, bona fide agents, and Federally Funded Research and Development Centers. This range suggests the CDC wanted applicants that could credibly reach diverse communities and either access or build population-level data sources capable of supporting standardized surveillance and disparity-focused analyses.

Overall, the opportunity was designed to help communities and public health partners produce stronger, more consistent epidemiologic evidence on epilepsy and its drivers, then use that evidence to guide practical actions in prevention and care systems. For administrative questions, the announcement listed Kenya N. Anderson, Grants Management Specialist at the CDC, with telephone contact at (770) 488-2487.

Frequently Asked Questions (FAQs)

What is the name of this grant opportunity?

The opportunity is titled "Improving Surveillance and Prevention of Epilepsy Burden in US Communities."

What is the Funding Opportunity Number (FON)?

The Funding Opportunity Number is RFA DP 15 009.

Which federal agency offered this funding opportunity?

This was a CDC (Centers for Disease Control and Prevention) discretionary funding announcement.

What type of funding mechanism was used?

The funding mechanism was a cooperative agreement.

What does it mean that this was a cooperative agreement?

Because it was a cooperative agreement, the CDC would typically expect substantial involvement in the project beyond issuing funds, such as collaboration on methods, measures, and/or dissemination strategies.

What was the central aim of the opportunity?

The central aim was to strengthen epilepsy public health surveillance by applying standardized definitions and consistent methods so that estimates and findings are comparable across communities and over time.

What kinds of epilepsy measures was the CDC trying to improve?

The announcement emphasized generating clearer, more reliable information about epilepsy prevalence (how many people have epilepsy) and/or incidence (how many new cases occur over a given period), including within specific U.S. populations and subpopulations.

Was the focus only on counting cases?

No. The CDC framed the work as more than counting cases. Applicants were expected to use surveillance-quality data to expand knowledge about determinants of epilepsy outcomes, including risk factors and other influences shaping incidence, prevalence, and related outcomes.

Why was standardization emphasized?

Standardized definitions and consistent methods were emphasized so that findings and estimates could be compared across different communities and tracked over time.

Did the opportunity emphasize health disparities?

Yes. A major emphasis was addressing health disparities, including improving measurement and understanding of epilepsy burden in populations and subpopulations where it may be undermeasured or unevenly distributed.

How were project findings intended to be used?

The intent was that stronger evidence on who is affected, where, and why would inform better-targeted interventions and services related to prevention, treatment support, and rehabilitation, with the broader goal of reducing inequities and minimizing disproportionate impact.

What program category or activity area did this fall under?

The announcement was in the health activity category.

What CFDA number was associated with this opportunity?

The opportunity was tied to CFDA 93.068 (Chronic Diseases Research, Control, and Prevention).

Was cost sharing or matching required?

No. The announcement stated there was no cost sharing or matching requirement.

How much total funding was estimated for this opportunity?

The estimated total funding amount was $1,800,000.

What was the maximum award amount per award (award ceiling)?

The award ceiling was $300,000.

What was the minimum award amount (award floor)?

The award floor was listed as $0.

How many awards did the CDC anticipate making?

The CDC anticipated making two awards.

When was this opportunity posted?

The posting date was December 23, 2014.

Was a Letter of Intent (LOI) required, and when was it due?

A Letter of Intent deadline was listed. It was due January 26, 2015.

When was the full application due?

The full application was due February 26, 2015, by 5:00 PM Eastern.

Is this funding opportunity still open?

No. The opportunity later moved to archive status on March 28, 2015, meaning it was no longer accepting applications after that cycle.

Who was eligible to apply?

Eligibility was broad and included: Hispanic-serving Institutions; Historically Black Colleges and Universities; Tribally Controlled Colleges and Universities; Alaska Native and Native Hawaiian Serving Institutions; eligible federal agencies; U.S. territories or possessions; faith-based and community-based organizations; regional organizations; bona fide agents; and Federally Funded Research and Development Centers.

Why did the eligibility list include so many institution types?

The eligibility scope suggests the CDC wanted applicants positioned to reach underserved or priority populations and to access or build population-level data sources that support standardized surveillance and disparity-focused analyses.

What kinds of communities or populations were especially relevant?

The announcement highlighted work within specific U.S. populations and subpopulations where epilepsy burden may be undermeasured or unevenly distributed, consistent with its emphasis on health disparities.

What was the overall public health purpose behind the surveillance work?

The overall purpose was to help communities and public health partners produce stronger, more consistent epidemiologic evidence on epilepsy and its drivers, then use that evidence to guide practical actions in prevention and care systems.

Who was the listed contact for administrative questions?

The administrative contact listed was Kenya N. Anderson, Grants Management Specialist at the CDC.

What phone number was provided for the administrative contact?

The telephone number provided was (770) 488-2487.

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