Opportunity Information: Apply for RFA DA 24 010

The National Institutes of Health (NIH) funding opportunity titled "Rapid Translation of Epidemiological Findings into Interventions to Prevent Substance Use and Addiction (R61/R33 Clinical Trial Optional)" (RFA-DA-24-010; CFDA 93.279) is designed to speed up the path from epidemiology to real-world prevention strategies for substance use and addiction. The core problem it targets is that epidemiologic findings often stay in the realm of observation and risk-factor identification and do not reliably translate into prevention interventions that can be tested, refined, and implemented. This initiative aims to change those incentives by explicitly tying epidemiologic discovery to the development, adaptation, or targeting of prevention interventions.

The opportunity uses a phased grant mechanism, R61/R33, to support a structured pipeline from data to action. In the R61 phase (the early, exploratory stage), awardees conduct innovative epidemiologic research focused on substance use and addiction. That epidemiologic work can be based on primary data collection, secondary analysis of existing datasets, or other rigorous approaches that can generate credible, actionable prevention hypotheses. The expectation is that the R61 phase does not end with descriptive findings alone; it must generate a clear foundation for what should be changed, for whom, and why, in order to prevent substance use initiation, escalation, or related harms.

The R33 phase (the later, implementation-oriented stage) is where the translation happens. Projects are expected to apply the R61 findings directly to a targeted prevention intervention. Applicants can take one of two main approaches. First, they may adapt or more precisely target an existing intervention to increase its effect size, improve its fit, or extend its reach to a new or underserved population. Second, they may develop a novel intervention aimed at a new prevention target that emerged from the epidemiologic evidence in R61. In either case, the goal is not simply to conduct another observational study, but to use epidemiologic results to inform an intervention strategy that can be tested, optimized, and positioned for broader prevention impact. The "Clinical Trial Optional" designation indicates that a clinical trial may be proposed if it fits the project goals, but it is not required for all applications.

A key structural requirement is the use of a Multiple Principal Investigator/Multiple Project Director (MPI/MPD) leadership model. This reflects the program's emphasis on bridging disciplines that often operate separately. Applicants must assemble leadership with the expertise to drive both the epidemiologic components and the prevention intervention components, ensuring that the project is equipped to move from identifying risk and protective factors to designing practical, testable prevention solutions. In practice, this means the team should be able to credibly handle epidemiologic methods, prevention science, intervention development or adaptation, implementation considerations, and the analytic strategy that connects the phases.

The announcement also highlights a supplement mechanism intended to promote "bidirectional" translational science. This means translation is not treated as a one-way street from epidemiology to intervention. Existing epidemiologic projects may seek support to test prevention hypotheses that emerge from their data, while existing prevention intervention projects may request added epidemiologic inquiry to better interpret, contextualize, or refine their findings. The intent is to create a feedback loop where observational data informs intervention design, and intervention results generate new epidemiologic questions that sharpen understanding of who benefits, under what conditions, and through what mechanisms.

Eligibility is broad and includes many types of organizations and institutions that could contribute to prevention research. Eligible applicants include various levels of government (state, county, city/township, special districts), independent school districts, public and state-controlled institutions of higher education, private institutions of higher education, federally recognized Native American tribal governments, and Native American tribal organizations that are not federally recognized tribal governments. Nonprofits are eligible whether or not they have 501(c)(3) status, and both for-profit organizations (other than small businesses) and small businesses may apply. The announcement also explicitly calls out additional eligible groups such as Alaska Native and Native Hawaiian Serving Institutions, Asian American Native American Pacific Islander Serving Institutions (AANAPISISs), Hispanic-serving Institutions, Historically Black Colleges and Universities (HBCUs), Tribally Controlled Colleges and Universities (TCCUs), faith-based or community-based organizations, regional organizations, eligible federal agencies, U.S. territories or possessions, and even non-U.S. entities (foreign organizations). This breadth signals an interest in supporting prevention solutions that can be culturally and contextually grounded and that address diverse populations and settings.

From a practical standpoint, the opportunity sets an award ceiling of $500,000, and it was created on December 12, 2022, with an original closing date listed as March 15, 2023. Overall, the funding call is built around a clear expectation: generate strong epidemiologic evidence in the first phase, then use it to drive a concrete prevention intervention strategy in the second phase, with leadership and team structure explicitly designed to prevent the work from stalling at discovery and to push it toward measurable prevention impact.

  • The National Institutes of Health in the education, health sector is offering a public funding opportunity titled "Rapid Translation of Epidemiological Findings into Interventions to Prevent Substance Use and Addiction (R61/R33 Clinical Trial Optional)" and is now available to receive applicants.
  • Interested and eligible applicants and submit their applications by referencing the CFDA number(s): 93.279.
  • This funding opportunity was created on 2022-12-12.
  • Applicants must submit their applications by 2023-03-15. (Agency may still review applications by suitable applicants for the remaining/unused allocated funding in 2026.)
  • Each selected applicant is eligible to receive up to $500,000.00 in funding.
  • Eligible applicants include: State governments, County governments, City or township governments, Special district governments, Independent school districts, Public and State controlled institutions of higher education, Native American tribal governments (Federally recognized), Public housing authorities/Indian housing authorities, Native American tribal organizations (other than Federally recognized tribal governments), Nonprofits having a 501 (c) (3) status with the IRS, other than institutions of higher education, Nonprofits that do not have a 501 (c) (3) status with the IRS, other than institutions of higher education, Private institutions of higher education, For-profit organizations other than small businesses, Small businesses, Others.
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FAQs: NIH Rapid Translation of Epidemiological Findings into Interventions to Prevent Substance Use and Addiction (R61/R33 Clinical Trial Optional)

What is this funding opportunity?

This is a National Institutes of Health (NIH) funding opportunity titled "Rapid Translation of Epidemiological Findings into Interventions to Prevent Substance Use and Addiction (R61/R33 Clinical Trial Optional)" (RFA-DA-24-010; CFDA 93.279). It supports projects that move quickly from epidemiological findings to real-world prevention interventions for substance use and addiction.

What problem is the program trying to solve?

The program targets a common gap in the field: epidemiologic findings often remain observational (identifying risk and protective factors) and do not consistently translate into prevention interventions that can be tested, refined, and implemented. This opportunity is designed to change those incentives by explicitly linking epidemiologic discovery to intervention development, adaptation, or targeting.

What does "rapid translation" mean in this context?

What grant mechanism does this program use?

It uses a phased R61/R33 mechanism. The R61 phase supports early, exploratory epidemiologic research. The R33 phase supports the later translation of R61 findings into a targeted prevention intervention.

What is the purpose of the R61 phase?

The R61 phase is the early, exploratory stage where awardees conduct innovative epidemiologic research focused on substance use and addiction. This work may use primary data collection, secondary analysis of existing datasets, or other rigorous epidemiologic approaches, as long as it produces credible, actionable prevention hypotheses.

What outcomes are expected by the end of the R61 phase?

The R61 phase is expected to produce more than descriptive findings. It should generate a clear foundation for what should be changed, for whom, and why, to prevent substance use initiation, escalation, or related harms. The R61 findings should directly inform the prevention intervention strategy planned for the R33 phase.

What is the purpose of the R33 phase?

The R33 phase is where translation happens. Projects are expected to apply the R61 findings directly to a targeted prevention intervention, with the intention of testing and optimizing the strategy and positioning it for broader prevention impact.

What kinds of prevention intervention approaches are supported in R33?

Two main approaches are described:

  • Adapt or more precisely target an existing intervention to increase effect size, improve fit, or extend reach to a new or underserved population.
  • Develop a novel intervention aimed at a new prevention target that emerged from the epidemiologic evidence produced in the R61 phase.

Does the project need to include a clinical trial?

No. The opportunity is labeled "Clinical Trial Optional," meaning a clinical trial may be proposed if it matches the project goals, but a clinical trial is not required for every application.

Is the program mainly about conducting observational research?

No. While the R61 phase supports epidemiologic research, the overall purpose is to move beyond observation and use the findings to drive an intervention strategy in the R33 phase. The program emphasizes actionability and translation into prevention solutions.

What leadership structure is required?

A Multiple Principal Investigator/Multiple Project Director (MPI/MPD) leadership model is required. This requirement reflects the program's goal of bridging disciplines to ensure the project can execute both rigorous epidemiology and practical prevention intervention work.

Why does the program require an MPI/MPD model?

The announcement emphasizes that epidemiology and prevention intervention work often sit in different disciplines. Requiring multiple leaders is intended to ensure the project has credible expertise to move from identifying risk/protective factors to designing and testing prevention solutions, rather than stalling at discovery.

What kinds of expertise should the leadership team cover?

Based on the program description, leadership should be able to drive both phases, including epidemiologic methods, prevention science, intervention development or adaptation, implementation considerations, and an analytic strategy that connects the R61 findings to the R33 intervention.

What does "bidirectional translational science" mean here?

Bidirectional translation means the flow of learning goes both ways: epidemiologic data informs intervention design, and intervention results generate new epidemiologic questions. The intent is a feedback loop that improves understanding of who benefits, under what conditions, and through what mechanisms.

What is the supplement mechanism mentioned in the announcement?

The announcement highlights a supplement mechanism intended to promote bidirectional translational science. It supports adding work that strengthens the link between epidemiology and prevention interventions, creating a feedback loop between observational evidence and intervention outcomes.

Who can use the supplement mechanism?

Two situations are described:

  • Existing epidemiologic projects may seek added support to test prevention hypotheses that emerge from their data.
  • Existing prevention intervention projects may request added epidemiologic inquiry to better interpret, contextualize, or refine their findings.

Who is eligible to apply?

Eligibility is broad. Eligible applicants include many organization types, including various levels of government (state, county, city/township, special districts), independent school districts, public and state-controlled institutions of higher education, private institutions of higher education, federally recognized Native American tribal governments, and Native American tribal organizations that are not federally recognized tribal governments.

Are nonprofits eligible?

Yes. Nonprofits are eligible whether or not they have 501(c)(3) status, based on the eligibility list provided.

Are for-profit organizations eligible?

Yes. For-profit organizations (other than small businesses) and small businesses are both listed as eligible.

Are community-based or faith-based organizations eligible?

Yes. The eligibility list explicitly includes faith-based or community-based organizations.

Are minority-serving institutions specifically included?

Yes. The eligibility list explicitly mentions Alaska Native and Native Hawaiian Serving Institutions, Asian American Native American Pacific Islander Serving Institutions (AANAPISISs), Hispanic-serving Institutions, Historically Black Colleges and Universities (HBCUs), Tribally Controlled Colleges and Universities (TCCUs), and other groups.

Are U.S. territories or possessions eligible?

Yes. U.S. territories or possessions are explicitly included in the eligible applicant types.

Are non-U.S. (foreign) organizations eligible?

Yes. The announcement explicitly includes non-U.S. entities (foreign organizations) as eligible.

How much funding is available per award?

The opportunity sets an award ceiling of $500,000.

When was the opportunity created and what is the listed closing date?

The opportunity was created on December 12, 2022, and the original closing date listed is March 15, 2023.

What is the overall expectation for a successful project?

The core expectation is a two-phase progression: generate strong, innovative epidemiologic evidence in the R61 phase, then use that evidence to drive a concrete, targeted prevention intervention strategy in the R33 phase, supported by an MPI/MPD leadership structure designed to keep the work moving from discovery to measurable prevention impact.

What health topic area does this program focus on?

The program focuses on preventing substance use and addiction, including preventing initiation, escalation, and related harms.

What is the program trying to encourage in terms of intervention impact?

It is designed to encourage interventions that are better targeted, better fitting for specific contexts or populations, and able to extend reach to new or underserved groups, or entirely new interventions that address prevention targets identified through epidemiology.

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