Opportunity Information: Apply for W81XWH 13 PCRP PSIA

  • The Dept. of the Army USAMRAA in the science and technology and other research and development sector is offering a public funding opportunity titled "DoD Prostate Cancer Population Science Impact Award" and is now available to receive applicants.
  • Interested and eligible applicants and submit their applications by referencing the CFDA number(s): 12.420 Military Medical Research and Development.
  • This funding opportunity was created on Jun 15, 2013 and posted on Jun 15, 2013.
  • Applicants must submit their applications by Oct 9, 2013. (Agency may still review applications by suitable applicants for the remaining/unused allocated funding in 2026.)
  • The funding agency has allocated a total of $2,400,000.00 to eligible and selected applicants.
  • The number of recipients for this funding is limited to 2 candidate(s).
  • Eligible applicants include: Unrestricted (i.e., open to any type of entity above), subject to any clarification in text field entitled Additional Information on Eligibility.
Apply for W81XWH 13 PCRP PSIA

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Opportunity Summary:

The DoD Prostate Cancer Research Program (PCRP) Population Science Impact Award (PSIA) is a funding opportunity from the Department of the Army (USAMRAA) designed to support high-impact population science research that can meaningfully reduce deaths from prostate cancer and/or improve quality of life for men living with the disease. This mechanism has evolved over time (previously offered as the Population Based Idea Development Award and Population Based Research Award), and it is positioned as a competitive, impact-driven program aimed at studies that can influence prostate cancer outcomes at the population level rather than through work focused only on individual patients. The announcement emphasizes that proposed projects should be strong enough to substantially advance the field and should clearly explain why the expected findings would matter for large groups of men, such as those represented in cohorts, health systems, or defined communities.

A central expectation is that applications align with the PCRP's overarching challenges or, if not, make a clear case that they address another critical prostate cancer research need. The program particularly encourages projects connected to several priority focus areas: biomarkers (especially those tied to aggressive disease), genetics and genomics, therapy and predictors of treatment response or resistance, and survivorship and palliative care. Research that addresses disparities in prostate cancer incidence, morbidity, or mortality is also explicitly encouraged, reflecting the program's interest in studies that can help explain and reduce unequal burdens of disease across populations.

The award is intended for systematic population-based studies grounded in established population science disciplines and methods. The announcement lists epidemiology, surveillance, health services research, outcomes research, behavioral science, social science, and dissemination research as relevant approaches, while leaving room for other population science frameworks. The goal is to generate data, evidence, and/or tools that are only feasible when studying groups at scale, such as identifying population-level risk patterns, evaluating real-world care and outcomes, understanding behavioral or social drivers of screening and treatment decisions, or testing strategies to spread effective practices across healthcare settings.

In terms of study design, the opportunity supports a range of population science methodologies, including retrospective studies, prospective studies, case-control designs, cohort studies, and other suitable approaches. The use of biospecimens and data from established retrospective databases is allowed, as long as the proposed sample size is large enough to support statistically significant findings. Reviewers are expected to look for a clearly articulated and conceptually sound hypothesis that is specific to prostate cancer, and for a study plan that demonstrates serious statistical rigor. Applicants are expected to spell out the statistical expertise on the research team and to present an analysis plan that makes it clear the team can appropriately handle population-level data, bias and confounding concerns, and the complexities of drawing valid conclusions from large datasets.

Human subjects research is permitted, but the opportunity explicitly restricts funded projects to studies that do not involve clinical trials. At the same time, the announcement allows correlative studies that use populations from existing clinical trials, meaning researchers can analyze already-generated clinical trial data or specimens to answer new population-oriented questions without conducting a new trial under this award. The announcement points applicants to CDMRP human subjects guidance materials for definitions and clarifications, which matters because CDMRP draws specific lines between clinical research, clinical trials, and other human subjects studies.

Applicants are also expected to show they can actually access the populations, samples, and datasets they propose to use. That includes providing documentation demonstrating access to appropriate patient populations, recruitment capability when applicable, and sufficient numbers of participants or records to achieve statistical significance. This emphasis on demonstrated access reflects the program's practical concern that population science projects can fail if they lack reliable pipelines to data, biospecimens, or community and health system partnerships.

To strengthen applications and encourage resource sharing, the PCRP suggests leveraging established PCRP-supported resources when relevant, including the Prostate Cancer Biorepository Network (PCBN) and the North Carolina-Louisiana Prostate Cancer Project (PCaP). These resources can be particularly useful for studies requiring retrospectively collected human specimens or linked clinical and demographic data, and they align with the program's preference for studies that can scale and generalize across real populations.

The award is offered as a Cooperative Agreement/Grant under CFDA 12.420 (Military Medical Research and Development). The posted opportunity (W81XWH-13-PCRP-PSIA) anticipated making about two awards, with an estimated total funding amount of $2.4 million and no cost sharing requirement. Eligibility is described as unrestricted, meaning a wide range of organizations may apply, subject to any additional clarifications in the full announcement.

Finally, the program signals an expectation of broad data and resource sharing. CDMRP states that data and research resources generated through funded projects should be made available to the wider research community, including consumer advocacy communities, and to the public, consistent with CDMRP guidance. In practice, this means applicants should be prepared to describe how they will manage, document, and share datasets, tools, and other products in ways that support transparency, reuse, and downstream impact beyond the original study team.

DoD Prostate Cancer Research Program (PCRP) Population Science Impact Award (PSIA) - FAQs

What is the PCRP Population Science Impact Award (PSIA)?

The PSIA is a Department of Defense (DoD) Prostate Cancer Research Program funding opportunity (managed by the Department of the Army/USAMRAA) that supports high-impact population science research intended to reduce deaths from prostate cancer and/or improve quality of life for men living with the disease.

What is the main goal of this award?

The goal is to fund rigorous, population-level studies that can meaningfully influence prostate cancer outcomes for large groups of men (for example, cohorts, health systems, or defined communities), rather than focusing only on outcomes for individual patients.

How is this award different from patient-level research funding?

This mechanism emphasizes population science questions and methods, such as identifying risk patterns across large groups, evaluating real-world care and outcomes, and understanding social or behavioral drivers of screening and treatment decisions.

Has this award mechanism been offered under other names before?

Yes. The mechanism has evolved over time and was previously offered as the Population Based Idea Development Award and the Population Based Research Award.

What kinds of research areas are encouraged?

The announcement particularly encourages population science projects connected to priority focus areas including biomarkers (especially those tied to aggressive disease), genetics and genomics, therapy and predictors of treatment response or resistance, and survivorship and palliative care.

Are projects addressing prostate cancer disparities encouraged?

Yes. Research that addresses disparities in prostate cancer incidence, morbidity, or mortality is explicitly encouraged, reflecting an interest in understanding and reducing unequal burdens of disease across populations.

Do projects need to align with PCRP overarching challenges?

Applications are expected to align with the PCRP overarching challenges or, if not aligned, to make a clear case that they address another critical prostate cancer research need.

What population science disciplines and approaches fit this award?

The opportunity identifies epidemiology, surveillance, health services research, outcomes research, behavioral science, social science, and dissemination research as relevant approaches, while also leaving room for other population science frameworks.

What types of study designs are supported?

The program supports a range of population science study designs and methodologies, including retrospective studies, prospective studies, case-control designs, cohort studies, and other suitable approaches.

Can applicants use existing databases and retrospective resources?

Yes. The use of biospecimens and data from established retrospective databases is allowed, as long as the proposed sample size is large enough to support statistically significant findings.

Does the research need a specific hypothesis?

Yes. Reviewers are expected to look for a clearly articulated and conceptually sound hypothesis that is specific to prostate cancer.

How important is statistical rigor in the application?

Statistical rigor is a central expectation. Applicants are expected to describe the statistical expertise on the team and provide an analysis plan demonstrating the ability to manage population-level data, bias and confounding, and the complexities of valid inference from large datasets.

Is human subjects research allowed?

Yes. Human subjects research is permitted under this opportunity, consistent with CDMRP human subjects guidance and definitions.

Are clinical trials allowed under this award?

No. Funded projects are restricted to studies that do not involve clinical trials.

Can the project use data or specimens from existing clinical trials?

Yes. Correlative studies using populations from existing clinical trials are allowed. That means researchers may analyze already-generated clinical trial data or specimens to answer new population-oriented questions without conducting a new clinical trial under this award.

Do applicants need to prove access to populations, samples, or datasets?

Yes. Applicants are expected to demonstrate that they can access the proposed populations, samples, and datasets. This includes documentation showing access to appropriate patient populations, recruitment capability when applicable, and sufficient participant or record counts to achieve statistical significance.

Does the program recommend using any established PCRP resources?

Yes. When relevant, the PCRP suggests leveraging PCRP-supported resources such as the Prostate Cancer Biorepository Network (PCBN) and the North Carolina-Louisiana Prostate Cancer Project (PCaP).

Why might PCBN or PCaP be useful for a PSIA project?

These resources can support studies requiring retrospectively collected human specimens or linked clinical and demographic data, and they align with the program preference for population-scale studies that can generalize across real populations.

What is the funding mechanism and CFDA number?

The award is offered as a Cooperative Agreement/Grant under CFDA 12.420 (Military Medical Research and Development).

What is the posted opportunity identifier?

The posted opportunity referenced is W81XWH-13-PCRP-PSIA.

How many awards and how much total funding were anticipated?

The posting anticipated making about two awards, with an estimated total funding amount of $2.4 million.

Is cost sharing required?

No. The posting states there is no cost sharing requirement.

Who is eligible to apply?

Eligibility is described as unrestricted, meaning a wide range of organizations may apply, subject to any additional clarifications in the full announcement.

Is there an expectation to share data and resources created by the project?

Yes. CDMRP indicates that data and research resources generated through funded projects should be made available to the wider research community (including consumer advocacy communities) and to the public, consistent with CDMRP guidance.

What should applicants be prepared to include regarding sharing?

Applicants should be prepared to describe how they will manage, document, and share datasets, tools, and other products in ways that support transparency, reuse, and broader impact beyond the original study team.

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