Opportunity Information: Apply for W81XWH 19 OPORP CRA
The DoD Orthotics and Prosthetics Outcomes Research Program (OPORP) Clinical Research Award (CRA) is a Department of Defense funding opportunity aimed at improving real-world care for people with limb loss or limb impairment, with a clear emphasis on Service members and Veterans. The central goal is to fund clinical research that compares and evaluates existing orthotic and prosthetic device options using patient-centric outcomes, meaning outcomes that matter directly to users in daily life. Rather than asking researchers to invent a new component or engineer a next-generation device, this program is designed to answer practical clinical questions such as which currently available devices work best, for whom, and under what conditions.
A defining feature of this award is its focus on outcomes-based best practices. The program is essentially challenging the field to produce stronger evidence that can guide evidence-based practice in orthotics and prosthetics. That includes identifying which device types, configurations, and device characteristics are linked to better patient outcomes. In this context, "best" is not limited to laboratory performance; it is tied to patient-relevant measures that can influence clinical decision-making and optimize care, such as function, mobility, comfort, quality of life, participation in work and community activities, satisfaction, and other clinically meaningful endpoints appropriate to the limb loss or limb impairment population.
The scope is intentionally translational in the sense that it targets clinical relevance and near-term applicability. Studies should be structured to inform clinicians, health systems, and policymakers about how to choose among options that are already on the market and in use. This makes the opportunity especially suited for comparative effectiveness research, pragmatic clinical studies, and outcomes analyses that can clarify which device features or prescribing approaches lead to better results in specific subgroups. The program explicitly steers applicants away from proposals centered on technology development or incremental engineering improvements, keeping the spotlight on clinical evaluation and decision-making evidence.
Collaboration is strongly encouraged, especially multidisciplinary partnerships that bring together academia, industry, military medical organizations, the Department of Veterans Affairs, and other federal agencies. The intent is to leverage complementary strengths such as clinical populations and care settings, device and manufacturing expertise, rehabilitation research methods, and implementation pathways within military and Veteran health systems. Proposals that reflect these kinds of cross-sector collaborations are aligned with the program's stated preference for team-based approaches that can accelerate the use of findings in practice.
The FY19 OPORP CRA offers two funding levels, and applicants must choose only one level per application. Funding Level 1 is geared toward pilot studies that can still make meaningful progress toward clinical translation; preliminary data are permitted but not required, making it a fit for well-justified early-stage clinical outcome studies with a strong design and a clear path to impact. Funding Level 2 is intended for studies that already have preliminary data and are positioned to make significant advancements toward clinical translation, reflecting a higher expectation of readiness and evidentiary foundation.
Administratively, the opportunity was issued by the Department of Defense, Department of the Army, through USAMRAA, under Funding Opportunity Number W81XWH-19-OPORP-CRA, with assistance mechanisms listed as cooperative agreements and grants and an R and D-focused activity category. Eligibility is described as unrestricted, meaning a wide range of organization types may apply, subject to any additional clarifications in the full announcement. The program anticipated making about six awards, and while an award ceiling is listed as 0 in the provided source data, that typically indicates that specific budget limits are defined elsewhere in the full solicitation or vary by proposal category and negotiated scope. The key requirement across all applications is relevance: the proposed work must be directly applicable to active duty Service members, Veterans, military beneficiaries, and/or the broader American public, ensuring that funded outcomes research translates into practical benefits for these populations.Apply for W81XWH 19 OPORP CRA
- The Department of Defense, Dept. of the Army -- USAMRAA in the science and technology and other research and development sector is offering a public funding opportunity titled "DoD Orthotics and Prosthetics Outcomes Research Program, Clinical Research Award" and is now available to receive applicants.
- Interested and eligible applicants and submit their applications by referencing the CFDA number(s): 12.420.
- This funding opportunity was created on Jun 19, 2019.
- Applicants must submit their applications by Aug 07, 2019. (Agency may still review applications by suitable applicants for the remaining/unused allocated funding in 2026.)
- The number of recipients for this funding is limited to 6 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.
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FAQs: DoD OPORP Clinical Research Award (CRA)
What is the OPORP Clinical Research Award (CRA)?
The Orthotics and Prosthetics Outcomes Research Program (OPORP) Clinical Research Award (CRA) is a Department of Defense funding opportunity that supports clinical research to improve real-world care for people with limb loss or limb impairment. It emphasizes research that can directly inform clinical decision-making, especially for Service members and Veterans.
What is the main goal of this award?
The central goal is to fund clinical research that compares and evaluates existing orthotic and prosthetic device options using patient-centric outcomes. The program is focused on generating evidence that helps answer practical questions like which currently available devices work best, for whom, and under what conditions.
What types of research questions is the program trying to answer?
The award is designed to support practical, clinically relevant questions, such as:
- How different existing device options compare in real-world use
- Which device types, configurations, or characteristics are linked to better outcomes
- How outcomes vary across different patient subgroups or care contexts
- Which prescribing approaches lead to better patient-relevant results
What does "patient-centric outcomes" mean in this opportunity?
Patient-centric outcomes are outcomes that matter directly to orthotic and prosthetic users in daily life, rather than only laboratory or technical performance measures. The opportunity highlights outcomes such as function, mobility, comfort, quality of life, participation in work and community activities, satisfaction, and other clinically meaningful endpoints appropriate to the limb loss or limb impairment population.
Is this opportunity intended to fund new device invention or engineering improvements?
No. The program explicitly steers applicants away from proposals centered on technology development or incremental engineering improvements. The intent is to evaluate and compare devices that are already on the market and in use, producing evidence to support outcomes-based best practices.
What kind of study designs fit this award?
The description indicates the opportunity is especially suited for comparative effectiveness research, pragmatic clinical studies, and outcomes analyses. Studies should be designed to generate near-term, clinically useful evidence that can inform clinicians, health systems, and policymakers about choosing among existing device options.
What does the program mean by "outcomes-based best practices"?
It refers to building stronger evidence that can guide evidence-based practice in orthotics and prosthetics. The emphasis is on identifying which device types, configurations, and characteristics are associated with better patient-relevant outcomes, with the intent that findings can influence real clinical decisions and optimize care.
Who is the intended beneficiary population?
The opportunity has a clear emphasis on Service members and Veterans. A key requirement is that the proposed work must be directly applicable to active duty Service members, Veterans, military beneficiaries, and/or the broader American public.
How translational is this award expected to be?
The scope is intentionally translational in the sense of clinical relevance and near-term applicability. The intent is for studies to inform decisions in real care settings, rather than focusing on early-stage device engineering or purely mechanistic work.
Are collaborations encouraged?
Yes. Multidisciplinary collaborations are strongly encouraged, particularly partnerships spanning academia, industry, military medical organizations, the Department of Veterans Affairs, and other federal agencies. The intent is to combine complementary strengths such as access to clinical populations and care settings, device expertise, rehabilitation research methods, and implementation pathways within military and Veteran health systems.
Does the opportunity prefer team-based approaches?
Yes. Proposals reflecting cross-sector, multidisciplinary teamwork are described as aligned with the program's preference for team-based approaches that can accelerate the adoption of findings in practice.
How many funding levels are available under this award?
There are two funding levels, and applicants must choose only one level per application.
What is Funding Level 1 intended for?
Funding Level 1 is geared toward pilot studies that can still make meaningful progress toward clinical translation. Preliminary data are permitted but not required, making it appropriate for well-justified early-stage clinical outcomes studies with a strong design and a clear path to impact.
What is Funding Level 2 intended for?
Funding Level 2 is intended for studies that already have preliminary data and are positioned to make significant advancements toward clinical translation. It reflects a higher expectation of readiness and evidentiary foundation compared with Level 1.
Is preliminary data required to apply?
It depends on the funding level selected. Preliminary data are permitted but not required for Funding Level 1. Funding Level 2 is intended for studies that already have preliminary data.
How many awards does the program anticipate making?
The program anticipated making about six awards.
Who issued the funding opportunity and under what identifier?
The opportunity was issued by the Department of Defense, Department of the Army, through USAMRAA. The Funding Opportunity Number is W81XWH-19-OPORP-CRA.
What assistance mechanisms are listed for this opportunity?
The listed assistance mechanisms include cooperative agreements and grants.
What type of activity does this funding opportunity support?
The activity category is described as research and development (R and D) focused.
Who is eligible to apply?
Eligibility is described as unrestricted, meaning a wide range of organization types may apply, subject to any additional clarifications in the full announcement.
Is there a stated maximum award amount (award ceiling)?
In the provided source data, the award ceiling is listed as 0. This typically indicates that specific budget limits are defined elsewhere in the full solicitation or may vary by proposal category and negotiated scope.
What is the most important application requirement emphasized in the description?
The key requirement emphasized is relevance. Proposed work must be directly applicable to active duty Service members, Veterans, military beneficiaries, and/or the broader American public, with outcomes research translating into practical benefits for those populations.
How should success be measured under this program?
Success is framed around clinically meaningful, patient-relevant outcomes that can guide evidence-based practice. The emphasis is on generating evidence that can be used in real-world decision-making about existing orthotic and prosthetic options.
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