Opportunity Information: Apply for RFA DP 15 007
Apply for RFA DP 15 007
- The Centers for Disease Control and Prevention in the health sector is offering a public funding opportunity titled "Effectiveness of Teen Pregnancy Prevention Programs Designed Specifically for Young Males" and is now available to receive applicants.
- Interested and eligible applicants and submit their applications by referencing the CFDA number(s): 93.297 Teenage Pregnancy Prevention Program 93.946 Cooperative Agreements to Support State Based Safe Motherhood and Infant Health Initiative Programs.
- This funding opportunity was created on Feb 21, 2015 and posted on Dec 23, 2014.
- Applicants must submit their applications by Mar 6, 2015 AMENDMENT I. NEW DUE DATES AND SPECIAL DATE Effectiveness of Teen PregnancyPrevention Programs Designed Specifically for Young MalesAMENDMENT I.New Letter of Intent Due Date February 6, 2015Application Due Date 03/06/2015AMENDMENT I.Application Due Date has been changed from March 3, 2015 to March 6, 2015Additional CFDA # 93.297. (Agency may still review applications by suitable applicants for the remaining/unused allocated funding in 2026.)
- The funding agency has allocated a total of $10,000,000.00 to eligible and selected applicants.
- Each selected applicant is eligible to receive up to $1,000,000.00 in funding.
- The number of recipients for this funding is limited to 3 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)
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Opportunity Summary:
This funding opportunity (RFA-DP-15-007) is a CDC-led cooperative agreement, developed in collaboration with the HHS Office of Adolescent Health, focused on building stronger evidence about teen pregnancy prevention approaches that are designed specifically for young males. The core goal is to rigorously test innovative interventions for males ages 15 to 24 that aim to reduce the risk of fathering a teen pregnancy, with an emphasis on programs that can realistically be delivered in real-world settings such as clinics, schools, community organizations, youth-serving programs, or correctional environments. The announcement makes clear that the work is meant to move beyond general youth pregnancy prevention by centering young men as the intended participants and by generating high-quality evidence about what works for them.
The program planned to fund up to three projects, each lasting five years, with total estimated funding of about $10 million and an award ceiling of $1,000,000. A key requirement is that at least one of the funded projects must evaluate an intervention specifically targeted to younger males ages 15 to 19, ensuring that the portfolio includes work directly relevant to adolescents rather than only older young adults. Because this is a cooperative agreement, awardees should expect substantial federal involvement typical of that mechanism, often including collaboration on monitoring, performance expectations, and the use and dissemination of resulting products.
Applicants were asked to apply under one of two pathways based on how ready their intervention is for a rigorous evaluation. Component A is for an existing intervention that already has promising process data and/or early indications of effectiveness, but has not yet been tested through a rigorous evaluation design. Component B is for an intervention that is partially developed and needs to be finalized before it can be evaluated; in other words, the project would include a development or refinement phase followed by a formal test. In both components, the expectation is not just to implement programming, but to put the intervention through an experimental evaluation approach, indicating a preference for designs capable of strong causal inference (for example, randomized or similarly robust experimental methods).
The work is structured around two required sets of activities. Part I is the evaluation work: conducting a rigorous experimental evaluation of the intervention and, if it proves effective, packaging the intervention so it can be replicated. A major deliverable is a final intervention package, including materials needed for implementation, that must be provided to CDC and OAH. The announcement explicitly notes that CDC and OAH must be able to reproduce, publish, and otherwise use the resulting materials for public health purposes, and to authorize others to do so, consistent with applicable grant regulations. That emphasis signals a strong federal interest in dissemination and scaling of proven approaches rather than leaving materials proprietary or difficult for other communities to adopt.
Part II focuses on training and technical assistance (TTA), which is mandatory alongside the evaluation. The intent is to ensure both high-quality implementation and a high-quality evaluation by building capacity where it is needed. The FOA distinguishes between internal TTA (support tailored to the grantee organization and project staff) and external TTA (support tailored to the project’s partner organizations, such as schools, clinics, or community-based partners responsible for delivering or supporting the intervention). Applications had to address both Part I and Part II to be considered responsive, meaning a proposal that only offered evaluation without a clear TTA strategy, or only offered programming without rigorous evaluation, would not meet the announcement’s requirements.
Eligibility was broad and included a range of institution types and organizational categories, such as Hispanic-serving institutions, HBCUs, tribally controlled colleges and universities, Alaska Native and Native Hawaiian serving institutions, eligible federal agencies, US territories or possessions, faith-based and community-based organizations, regional organizations, bona fide agents, and federally funded research and development centers. There was no cost-sharing or matching requirement. The opportunity was posted December 23, 2014, and later amended to extend deadlines: the letter of intent due date shifted to February 6, 2015, and the application due date to March 6, 2015 (by 5 PM Eastern). The CFDA numbers associated with the funding were 93.297 (Teenage Pregnancy Prevention Program) and 93.946 (Safe Motherhood and Infant Health initiatives), reflecting the broader public health and maternal/infant health context in which teen pregnancy prevention sits.
Overall, the opportunity is best understood as a federal effort to expand the evidence base for male-focused teen pregnancy prevention by funding a small number of long-term, rigorous studies, and by requiring that successful interventions be turned into well-documented, shareable packages. The combination of experimental evaluation, deliverable intervention materials, and structured training and technical assistance reflects an intention not only to learn what works, but to make it feasible for other systems and communities to implement proven strategies with fidelity.
Frequently Asked Questions (FAQs)
What is the funding opportunity RFA-DP-15-007 about?
RFA-DP-15-007 is a CDC-led cooperative agreement, developed in collaboration with the HHS Office of Adolescent Health (OAH), to build stronger evidence on teen pregnancy prevention approaches designed specifically for young males. The focus is on rigorously testing innovative interventions for males ages 15 to 24 to reduce the risk of fathering a teen pregnancy in real-world settings.
Who is the intended participant population for the interventions?
The interventions are intended for young males ages 15 to 24, with the explicit goal of reducing the risk of fathering a teen pregnancy. The announcement emphasizes centering young men as the intended participants rather than taking a general youth pregnancy prevention approach.
Is there a requirement to include younger adolescents (ages 15 to 19)?
Yes. At least one of the funded projects must evaluate an intervention specifically targeted to younger males ages 15 to 19, ensuring the funded portfolio includes work directly relevant to adolescents.
How many awards were expected and what is the overall funding level?
The program planned to fund up to three projects over five years, with total estimated funding of about $10 million.
What is the award ceiling?
The award ceiling listed in the opportunity is $1,000,000.
How long is the project period?
Each funded project was expected to last five years.
What makes this a cooperative agreement rather than a standard grant?
This opportunity uses a cooperative agreement mechanism, meaning awardees should expect substantial federal involvement typical of that mechanism. The description indicates this may include collaboration related to monitoring, performance expectations, and the use and dissemination of resulting products.
What kinds of settings are interventions expected to work in?
The opportunity emphasizes interventions that can realistically be delivered in real-world settings, including clinics, schools, community organizations, youth-serving programs, or correctional environments.
What are the two application pathways (Component A and Component B)?
Applicants were asked to apply under one of two pathways based on intervention readiness:
- Component A: For an existing intervention with promising process data and/or early indications of effectiveness, but not yet tested using a rigorous evaluation design.
- Component B: For an intervention that is partially developed and must be finalized before evaluation; projects include a development/refinement phase followed by a formal test.
Does the opportunity prioritize rigorous evaluation designs?
Yes. The expectation is to subject the intervention to an experimental evaluation approach, with a preference for designs capable of strong causal inference (for example, randomized or similarly robust experimental methods).
What are the required activity parts for funded projects?
Projects are structured around two required sets of activities:
- Part I: Evaluation - Conduct a rigorous experimental evaluation of the intervention and, if effective, package the intervention so it can be replicated.
- Part II: Training and Technical Assistance (TTA) - Provide mandatory training and technical assistance to support high-quality implementation and evaluation.
Is training and technical assistance (TTA) mandatory?
Yes. Part II (TTA) is mandatory alongside the evaluation work. Applications had to address both Part I and Part II to be considered responsive.
What is the difference between internal TTA and external TTA in this opportunity?
The FOA distinguishes between:
- Internal TTA: Support tailored to the grantee organization and project staff.
- External TTA: Support tailored to partner organizations involved in delivering or supporting the intervention (for example, schools, clinics, or community-based partners).
What key deliverable is required if an intervention proves effective?
A major deliverable is a final intervention package that includes materials needed for implementation. This package must be provided to CDC and OAH so the intervention can be replicated.
What rights do CDC and OAH have to use the intervention materials produced under the award?
The announcement notes that CDC and OAH must be able to reproduce, publish, and otherwise use the resulting materials for public health purposes, and to authorize others to do so, consistent with applicable grant regulations. This signals a strong emphasis on dissemination and scaling of proven approaches.
Can an application focus only on implementing programming without a rigorous evaluation?
No. The opportunity emphasizes not only implementation but rigorous experimental evaluation. A proposal offering programming without a rigorous evaluation would not meet the requirements described.
Can an application focus only on evaluation without a clear TTA plan?
No. The FOA states that applications had to address both the evaluation (Part I) and training/technical assistance (Part II) to be considered responsive.
Who was eligible to apply?
Eligibility was broad and included multiple institution types and organizational categories, including Hispanic-serving institutions, HBCUs, tribally controlled colleges and universities, Alaska Native and Native Hawaiian serving institutions, eligible federal agencies, US territories or possessions, faith-based and community-based organizations, regional organizations, bona fide agents, and federally funded research and development centers.
Was cost-sharing or matching required?
No. The opportunity states there was no cost-sharing or matching requirement.
When was the opportunity posted and what were the key due dates?
The opportunity was posted on December 23, 2014, and later amended to extend deadlines. The letter of intent due date shifted to February 6, 2015, and the application due date shifted to March 6, 2015 (by 5 PM Eastern).
What CFDA numbers are associated with this funding opportunity?
The CFDA numbers associated with the funding were 93.297 (Teenage Pregnancy Prevention Program) and 93.946 (Safe Motherhood and Infant Health initiatives).
What is the overall purpose of requiring an intervention package and TTA?
The structure reflects an intention to generate high-quality evidence about what works for young males and to make successful interventions feasible for other systems and communities to implement with fidelity, through well-documented, shareable materials and structured training and technical assistance.
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