Department of Health and Human Services
Participating Organizations
National Institutes of Health (NIH)
(http://www.nih.gov)
Components of Participating Organizations
Office of Behavioral and Social Sciences Research (OBSSR)
(http://obssr.od.nih.gov/content)
Fogarty International Center (FIC) (http://www.fic.nih.gov)
Eunice Kennedy Shriver National Institute for Child Health and Human Development (NICHD)
(http://www.nichd.nih.gov)
National Cancer Institute (NCI) (http://www.cancer.gov)
National Center for Complementary and
Alternative Medicine (NCCAM) (http://nccam.nih.gov)
National Heart Lung and Blood
Institute (NHLBI) (http://www.nhlbi.nih.gov/index.htm)
National Institute of Environmental Health Sciences (NIEHS)
(http://www.niehs.nih.gov)
National Institute of Mental Health (NIMH) (http://www.nimh.nih.gov)
National Institute on Aging (NIA)
(http://www.nia.nih.gov)
National Institute on Alcohol Abuse and Alcoholism (NIAAA)
(http://www.niaaa.nih.gov)
National Institute on Dental and Craniofacial Research (NIDCR)
(http://www.nidcr.nih.gov)
National Institute on Drug Abuse (NIDA)
(http://www.nida.nih.gov)
Office of Disease Prevention (ODP) (http://odp.od.nih.gov)
Office of Dietary Supplements (ODS) (http://ods.od.nih.gov)
Title: Using Systems Science Methodologies to Protect and Improve
Population Health (R21)
Announcement
Type
New
Update: The following update relating to this announcement has been issued:
Program
Announcement (PA) Number: PAR-08-224
NOTICE: Applications submitted in response
to this Funding Opportunity Announcement (FOA) for Federal assistance must be
submitted electronically through Grants.gov (http://www.grants.gov)
using the SF424 Research and Related (R&R) forms and the SF424 (R&R)
Application Guide.
APPLICATIONS MAY NOT BE SUBMITTED IN PAPER FORMAT.
This FOA must be read in conjunction with the application guidelines included with this announcement in Grants.gov/Apply for Grants (hereafter called Grants.gov/Apply).
A registration process is necessary before submission and applicants are highly encouraged to start the process at least four (4) weeks prior to the grant submission date. See Section IV.
Catalog of Federal Domestic Assistance Number(s)
Key Dates
Release/Posted Date: August 1, 2008
Opening Date: September 16, 2008
(Earliest date an application may be submitted to Grants.gov)
Letters of Intent Receipt
Date(s): September 16, 2008
NOTE: On-time submission requires that
applications be successfully submitted to Grants.gov no later than 5:00 p.m.
local time (of the applicant institution/organization).
Application Due Date(s): Standard dates apply, please see http://grants1.nih.gov/grants/funding/submissionschedule.htm
AIDS Application Due Date(s): Standard dates apply, please see http://grants1.nih.gov/grants/funding/submissionschedule.htm#AIDS.
Peer Review
Date(s): Standard dates apply, please see http://grants1.nih.gov/grants/funding/submissionschedule.htm#reviewandaward
Council Review
Date(s): Standard dates apply, please see http://grants1.nih.gov/grants/funding/submissionschedule.htm#reviewandaward
Earliest Anticipated
Start Date(s): Standard dates apply, please see http://grants1.nih.gov/grants/funding/submissionschedule.htm#reviewandaward
Additional
Information To Be Available Date (URL Activation Date): Not Applicable
Expiration Date: September 8, 2011
Due
Dates for E.O. 12372
Not Applicable
Additional
Overview Content
Executive Summary
Table of Contents
Part I Overview Information
Part II Full Text of Announcement
Section I. Funding Opportunity
Description
1. Research Objectives
Section II. Award Information
1. Mechanism of Support
2. Funds Available
Section III. Eligibility Information
1. Eligible Applicants
A. Eligible Institutions
B. Eligible Individuals
2. Cost Sharing or Matching
3. Other-Special Eligibility Criteria
Section IV. Application and Submission
Information
1. Request Application Information
2. Content and Form of Application Submission
3. Submission Dates and Times
A. Submission, Review, and
Anticipated Start Dates
1. Letter of Intent
B. Submitting an Application
Electronically to the NIH
C. Application Processing
4.
Intergovernmental Review
5. Funding Restrictions
6.
Other Submission Requirements and Information
Section V. Application Review Information
1. Criteria
2. Review and Selection Process
A. Additional Review Criteria
B. Additional Review Considerations
C. Resource Sharing Plan(s)
3. Anticipated Announcement and Award Dates
Section VI. Award Administration
Information
1. Award Notices
2. Administrative and National Policy Requirements
3.
Reporting
Section VII. Agency Contacts
1. Scientific/Research Contact(s)
2. Peer Review Contact(s)
3. Financial/Grants Management Contact(s)
Section VIII. Other Information
- Required Federal Citations
Part II - Full Text of Announcement
Section I. Funding Opportunity Description
1. Research Objectives
This FOA solicits
Exploratory/Developmental (R21) applications from institutions/organizations
that propose to apply one or more specific system science
methodologies to “policy resistant” public health problems and contribute
knowledge that will enhance effective decision making around the development of
and prioritization of policies, interventions, and programs to improve
population health in the U.S. and abroad, especially where resources are
limited and only a limited number of programs/policies/interventions can be
implemented. Systems science
methodologies, discussed in more
detail below, are specific methodologies that have been developed to understand
connections between a system’s structure and its behavior over time; these
methods are often capable of illuminating a range of “policy resistant
problems” where interventions, programs, or policies typically
have unexpected, unintended, or counter-intuitive consequences. A system, in this context,
refers to the particular configuration of all relevant entities, resources, and
processes that together adequately characterize the problem space under study
(i.e., a system is defined the boundaries that stakeholders use to determine
which facts/observations are relevant for their inquiry as well as the
interpretations/judgments that they use to guide decisions or actions) (Ulrich,
2002).
In responding to this FOA, applicants are encouraged to:
Complex Health Problems Systems Science Methodologies
Approximately 50% of premature deaths and 70% of chronic illnesses in U.S. are preventable by changing behavioral risk factors and the related social and physical systems necessary to achieve and sustain those changes (Mokdad et al., 2004). Indeed chronic diseases, which are reaching epidemic proportions worldwide with 80% of chronic disease deaths occurring in low- and middle-income countries, are largely preventable (Jamison, et al., 2006). Globally, up to 80% of premature deaths from heart disease, stroke and diabetes can be averted with known behavioral and pharmaceutical interventions (WHO, 2005). There is a growing recognition that most major threats to the public’s health - including cardiovascular disease, pulmonary disease, cancer, diabetes, mental health problems, HIV, substance abuse, violence, emerging infectious diseases, obesity, sedentary lifestyle, poor diet, sleep disorders, and more—are complex in the sense that each one arises from an intricate mix of behavioral, economic and social factors interacting with biological factors, as well as each other, over the lifespan and across an array of settings (e.g., home, school, workplace, neighborhood, etc.). For example, tobacco use and successful cessation are influenced by host of interrelated factors, including: the tobacco product itself (e.g., percent free-base nicotine content, presence or absence of menthol/other flavoring, and other product constituents), the person (e.g., genetic predisposition), influences on the person (peer influence, media exposure - both tobacco promotion and health messages, cultural norms, prior tobacco exposure, availability and usage of pharmacotherapy, history of quit attempts, presence of workplace smoking bans), and the tobacco industry (product design, marketing, pricing; for a discussion of the myriad of factors in tobacco control, see NCI, 2007).
Most of the problems related to human health and disease are dynamically and relationally complex. Such problems have typically been approached using correlation-based analytic methods (e.g., regression), which are useful for identifying linear relationships but are limited because of their inability to set up and test a web of causal relationships. While such methods can be valuable in providing detailed information about various aspects of the problem, used alone they are insufficient for addressing complex problems that are dynamic (i.e., change over time) and complex in terms of the large number of relationships in the system.
Systems science methodologies provide a way to address complex problems, while taking into account the “big picture” and context of such problems. These methods enable investigators to examine the dynamic interrelationships of variables at multiple levels of analysis (e.g., from cells to society) simultaneously (often through causal feedback processes), while also studying the impact on the behavior of the system as a whole over time (Midgely, 2003). They are also useful for making implicit assumptions about complex phenomena explicit, which exposes gaps in knowledge about the problem. Moreover, simulation modeling can be used to generate “alternative futures” allowing decision makers (e.g., policy makers) to simulate the impact of various policy decisions and how they play out over time before actually putting them into practice (Sterman, 2006). For example, insights gained by the use of simulation models can help policy makers choose the most effective option among competing strategies when resources for combating the problem are limited. Systems science methodologies are also extremely useful for understanding why programs and interventions fail to have their intended effects (and in the worst cases magnify the problem; Sterman, 2000).
Systems science methodologies can also be used to refine and reform systems of care to enable planners to identify impediments to implementing proven innovations in everyday treatment and prevention practice. Dynamic models can facilitate the adoption of proven new therapeutic and business practices to ensure effective interface within existing complex systems of care. Decision tools and models can be developed to discover unanticipated effects of change on barriers to treatment and prevention services access, gaps in resource allocation, new training requirements, insufficient inter-organizational linkages, and numerous other factors affecting healthcare systems improvements.
Specific examples of systems science methodologies include, but are not limited to: systems dynamics modeling (Sterman, 2000), agent based modeling (Epstein, 2006), discrete event simulation (Banks et al., 2005), network analysis (Wasserman & Faust, 1994; Scott, 2000), dynamic microsimulation modeling (e.g., Mitton, Sutherland & Weeks, 2000), and Markov modeling (Sonnenberg & Beck, 1993). These techniques (among others) are particularly well-suited for understanding connections between a system’s structure and its behavior over time; anticipating a range of plausible futures based on explicit scenarios for action or inaction in certain areas; identifying unintended or counter-intuitive consequences of interventions; evaluating both the short- and long-term effects of policy options; and guiding investments in new research or data collection to address critical information needs. Such tools have proven heuristic power, typically integrating data from multiple prior studies and surveillance systems, and can offer innovative solutions to seemingly intractable problems. For example, systems modeling can enhance decision making and policy decisions by showing how to strike a more effective balance between treatment and prevention approaches.
Many system modeling methodologies are not new and indeed are now used routinely in fields such as corporate management, economics, engineering, physics, energy, ecology, biology, and others precisely because these methods add value compared with alternative techniques or unaided decision-making. System-oriented methods have been slower to diffuse in health-related behavioral and social science. Not surprisingly, as the appreciation for the complexity of many problems in the public health sphere has grown, there have been calls recently to address public health problems with systems science (Gerberding, 2007; Homer & Hirsch, 2006; Mabry, et al. 2008; Madon, et al., 2007; Milstein, 2008). For instance, systems science methodologies have already begun to be employed for planning and preparing against acute threats to public health (Lasker, 2004) such as global spread of a pandemic flu (Germann, Kadau, Longini, & Macken, 2006).
About Policy
Resistance
Why do some public health problems seem intractable and resistant to the effects of planned interventions? Numerous well-known initiatives have greatly improved population health. But there are many other situations where health and social policy ventures ultimately were unsuccessful or made matters worse.
Typically
labeled unintended consequences, side-effects (i.e., a secondary and usually
adverse effect), or short-term results, our encounters with unsuccessful or
less than fully successful interventions are rarely studied systematically.
Those experiences cut across diverse content areas and their patterns and
precursors are not well defined. Moreover, this phenomenon is not unique to the
field of population health. The experience is so common, it has been given the
generic name "policy resistance," defined as follows:
Policy resistance is the tendency for a policy,
program, or an intervention to be delayed, diluted, or defeated by the
responses of people, organizations, or the natural environment to the
intervention itself. (adapted from Meadows, 1982).
(Note that policy resistance refers to “policy” in the broad sense to include
policies as well as the interventions and programs that flow from them). Responses
to significant health-related problems often fail to recognize and/or address
complex conditions that prevail in neighborhoods across the nation, or in the
health protection system at large. Thus it is increasingly important that we
understand policy resistance where it affects the public's health.
Here are three real-world examples of policy resistance operating in the public health domain:
1) Low tar/nicotine cigarettes were designed by cigarette manufacturers, and promoted by public health officials as a way to reduce the health hazards associated with smoking. Consumers compensated by smoking more of these “light” cigarettes per day than the regular kind, took longer, more frequent drags, and held the smoke in their lungs longer. These changes in consumer behavior defeated the product’s design so that ultimately the health threat to smokers remained (adapted from Sterman, 2006; for expanded treatment of this issue see NCI, 2001).
2) Supported by scientific studies, and promoted by the federal government, the food industry, health practitioners and the popular media, low fat diets became very popular in the 1980’s and ‘90’s. However this significant shift in dietary intake did not have the desired effect on the national trends of overweight and obesity. Despite their increasing intake of low-fat food items, Americans grew heavier over the ensuing decades, not thinner, and now population rates of overweight and obesity are at or near historic highs. No one had predicted that the food industry would produce such an array of low-fat but relatively high calorie foods, nor that Americans would overindulge in them. Evidence is mixed about whether the introduction of lower-fat foods actually caused people to gain more weight (i.e., by increasing overall caloric intake). But one thing seems certain, the policy of introducing these novel foods was not effective enough to stem the rising tide overweight and obesity across the country (for full treatment of this subject, see La Berge, 2008).
3) Highly
active antiretroviral therapy (HAART) works well to reduce mortality among
those living with HIV/AIDS. But since the advent of HAART in 1996, high-risk
sexual behaviors among men who have sex with men have markedly increased,
further increasing this group’s risk of contracting HIV/AIDS. Paradoxically,
some part of this increase in risk-taking behavior may have been triggered by
the availability of the new therapy itself by conveying an optimism that HIV is
not as devastating a diagnosis as it once was (see Sullivan, Drake, &
Sanchez, 2007 for an extensive list of references). While the causes of this
observed behavior change are likely multiply-determined (Elford, 2006), the
post-HAART increase in high-risk sexual behavior was somewhat unanticipated and
has contributed to a rebound in HIV incidence and the proliferation of
multiply-resistant strains of HIV. In some geographic populations this
increase in risky behavior appears to be significant enough to offset the beneficial
effects afforded by HAART (e.g., Bezemer et al, 2008). (This example was
adapted from Sterman, 2006; see also Imrie, et al., 2007).
Applicants are strongly encouraged to read a
fuller discussion of the concept of policy resistance by Sterman (2006).
Applications funded under this FOA are encouraged to extend the understanding of public health problems and contribute knowledge that will enhance effective decision making around the prioritization of policies, interventions, and programs, especially where resources are limited and only a limited number of programs/policies/interventions can be implemented.
The objectives of this research program are to provide funding for applicants to use system science methodologies to address one or more specific opportunities to protect and improve population health. Applicants are encouraged to plan projects that tackle “policy resistant” health problems (i.e., ones in which the effects of planned interventions tend to be delayed, diluted or defeated by responses of the system to the intervention itself) using a systems science methodology.
Methodological approaches sought under this FOA are those that seek to understand the bigger picture – i.e., a group of related components that comprise a “system” in which the problem can be defined by an explicit and testable causal hypothesis. Multi-method approaches are welcome. Methodologies employed should be capable of addressing multiple relationships and changes in the systems over time. Such approaches include but are not limited to: microsimulation modeling, agent-based modeling, system dynamics simulation modeling, network analysis, Markov modeling, and stochastic modeling. In addition, proposed research should be “problem-focused,” that is, the project outcomes should be directly applicable to the translation implementation, dissemination and adoption in one or more real-world settings. (For more on this topic, see p. 17-18 of the OBSSR strategic prospectus available at: http://obssr.od.nih.gov/Content/Strategic_Planning/Strategic+Plan_2007/ObssrIndex.htm) The results of the proposed project should be of the type that could inform decisions related to programs, policies, or interventions that are designed to impact the identified problem. Applicants are encouraged to form investigative teams that include members with expertise in the relevant systems science methodology (or methodologies), along with researchers with expertise related to the content area and the various components of the system under study, and where applicable, public health practitioners or others in charge of making decisions related to the policies/program/interventions under study. Note that it is possible that two or more of the above named qualities may be found in a single team member.
Examples of Research Topics Being Sought
The following are examples of research topics sought under this FOA; note that appropriate topics include but are not limited to those listed below.
Additional Resources related to this FOA:
References
Banks, J., Carson, J., Nelson, B., & Nicol, D. (2005). Discrete-event system simulation. 4th edition. Englewood Cliffs, New Jersey: Prentice Hall.
Bezemer, D., de Wolf, F., Boerlijst, M.C., van Sighem, A., Hollingsworth, T.D., Prins, M., Geskus, R.B., Gras, L., Coutinho, R.A., & Fraser, C. (2008). A resurgent HIV-1 epidemic among men who have sex with men in the era of potent antiretroviral therapy. AIDS;22(9):1071-7.
Elford J. (2006). Changing patterns of sexual behaviour in the era of highly active antiretroviral therapy. Current Opinion in Infect Disease;19(1):26-32.
Epstein, J. M. (2006). Generative Social Science: Studies in Agent-Based Computational Modeling. Princeton, N.J.: Princeton University Press.
Gerberding, J. (2007). Health Protectionomics: A New Science of People, Policy and Politics. , Public Health Grand Rounds, September 19, 2007. George Washington University School of Public Health and Health Services: Washington, D.C. Retrieved July 14, 2008 from http://www.kaisernetwork.org/health_cast/hcast_index.cfm?display=detail&hc=2349 click on “video” or “transcripts”.
Germann, T.C., Kadau, K., Longini, I.M., Jr, & Macken, C.A. (2006). Mitigation strategies for pandemic influenza in the United States. Proceedings of the National Academy of Sciences USA; 103(15):5935-40.
Homer, J.B. & Hirsch, G.B. (2006). System dynamics modeling for public health: background and opportunities. Am J Public Health; 96(3):452-8.
Imrie J., Elford, J., Kippax, S., & Hart, G.J. (2007). Biomedical HIV prevention--and social science. Lancet; 370(9581):10-1.
Jamison, D. T. et al. (eds) (2006). Priorities in Health. World Bank, Washington D.C. Available at http://www.dcp2.org.
La Berge AF. (2008). How the ideology of low fat conquered America. J Hist Med Allied Sci.;63(2):139-77.
Lasker RD. (2004). Redefining readiness: terrorism planning through the eyes of the public. New York, NY: The New York Academy of Medicine; September 14, 2004. http://www.cacsh.org/eptpp.html
Mabry, P. Olster, D., Morgan, G., & Abrams, D. (2008). Interdisciplinarity and Systems Science to Improve Population Health: A View from the NIH Office of Behavioral and Social Sciences Research. American Journal of Preventive Medicine; Vol 35, Supplement; pp.S211-S224. Available online at http://dx.doi.org/10.1016/j.amepre.2008.05.018.
Madon, T., Hofman, K.J., Kupfer, L., & Glass, R.I. (2007). Implementation Science. Science; 318: 1728-1729.
Meadows, D.H. (1982). Whole earth models and systems. CoEvolution Quarterly, Summer, 98-108.
Midgley, G. (Ed). (2003). Systems Thinking. Thousand Oaks, CA: Sage Publications.
Mitton, L., Sutherland, H., & Weeks, M. (2000). Microsimulation Modelling for Policy Analysis: Challenges and Innovations. University Press, Cambridge.
Milstein B. (2008). Hygeia's constellation: navigating health futures in a dynamic and democratic world. Atlanta, GA: Syndemics Prevention Network, Centers for Disease Control and Prevention. Available at http://www.cdc.gov/syndemics/monograph/index.htm
Mokdad, A.H., Marks, J.S., Stroup, D.F., & Gerberding, J.L. (2004). Actual causes of death in the United States, 2000. JAMA;291(10):1238-45. Review. Erratum in: JAMA. 2005 Jan 19;293(3):293-4, 298.
National Cancer Institute. (2001). Risks Associated with Smoking Cigarettes with Low Tar Machine-Measured Yields of Tar and Nicotine. Tobacco Control Monograph No. 13. Bethesda, MD: U.S. Department of Health and Human Services, National Institutes of Health, National Cancer Institute.
National Cancer Institute. (2007). Greater Than the Sum: Systems Thinking in Tobacco Control. Tobacco Control Monograph No. 18. Bethesda, MD: U.S. Department of Health and Human Services, National Institutes of Health, National Cancer Institute. NIH Pub. No. 06-6085.
Sullivan, P.S., Drake, A.J., & Sanchez, T.H. (2007). Prevalence of treatment optimism-related risk behavior and associated factors among men who have sex with men in 11 states, 2000-2001. AIDS Behav;11(1):123-9.
Scott J. (2000). Social network analysis: a handbook, 2nd edition. Thousands Oaks, CA: Sage Publications.
Sonnenberg, F.A. & Beck, J.R. (1993). Markov models in medical decision making: a practical guide. Medical Decision Making;13(4): 322-338.
Sterman, J.D. (2000). Business Dynamics. Systems Thinking and Modeling for a Complex World. Boston: McGraw-Hill.
Sterman, J.D. (2006). Learning from Evidence in a Complex World. American Journal of Public Health, 96(3): 505-514.
Ulrich W. Boundary critique. In: Daellenbach HG, Flood RL, editors. The Informed Student Guide to Management Science. London: Thomson; 2002. p. 41-42. http://www.geocities.com/csh_home/downloads/ulrich_2002a.pdf
Wasserman S., & Faust, K. (1994). Social network analysis: methods and applications. Cambridge, England: Cambridge University Press.
World Health Organization. (2005). Preventing Chronic Diseases: A Vital Investment (WHO, Geneva).
Purpose of the R21 Mechanism
The evolution and vitality of the behavioral and social sciences requires a constant infusion of new ideas, techniques, and points of view. These may differ substantially from current thinking or practice and may not yet be supported by substantial preliminary data. By using the R21 mechanism, the NIH seeks to foster the introduction of novel scientific ideas, model systems, tools, and methodologies that have the potential to substantially advance behavioral and social science research.
The R21 mechanism is intended to encourage new exploratory and developmental research projects. For example, such projects could assess the feasibility of a novel area of investigation or a new experimental system that has the potential to enhance health-related research. Another example could include the unique and innovative use of an existing methodology to explore a new scientific area. These studies may involve considerable risk but may lead to a breakthrough in a particular area, or to the development of novel techniques, agents, methodologies, models, or applications that could have a major impact on a field of biomedical, behavioral, or clinical research.
Applications for R21 awards should describe projects distinct from those supported through the traditional R01 mechanism. For example, long-term projects, or projects designed to increase knowledge in a well-established area, will not be considered for R21 awards. Applications submitted under this mechanism should be exploratory and novel. These studies should break new ground or extend previous discoveries toward new directions or applications. Projects of limited cost or scope that use widely accepted approaches and methods within well established fields are better suited for the R03 small grant mechanism. Information on the R03 program can be found at http://grants.nih.gov/grants/funding/r03.htm.
See Section VIII, Other Information
- Required Federal Citations, for policies related
to this announcement.
Section
II. Award Information
1.
Mechanism of Support
This FOA will use the NIH Exploratory/Developmental Research Grant (R21) award mechanism. The Project
Director/Principal Investigator (PD/PI) will be solely responsible for
planning, directing, and executing the proposed project.
This FOA uses “Just-in-Time” information concepts see SF424 (R&R) Application Guide). It also uses the modular as well as non-modular budget formats (see the “Modular Applications and Awards” section of the NIH Grants Policy Statement. Specifically, if you are submitting an application with direct costs in each year of $250,000 or less (excluding consortium Facilities and Administrative [F&A] costs), use the PHS398 Modular Budget component provided in the SF424 (R&R) Application Package and SF424 (R&R) Application Guide (see specifically Section 5.4, “Modular Budget Component,” of the Application Guide).
2. Funds Available
The total project period for an application submitted in
response to this funding opportunity may not exceed 2 years. Although the size
of award may vary with the scope of research
proposed, it is expected that applications will stay within the budgetary
guidelines for an exploratory/developmental project; direct costs are limited
to $275,000 over an R21 two-year period, with no more than $200,000 in direct costs allowed in any single year.
Applicants may request direct costs in $25,000 modules, up to the total direct
costs limitation of $275,000 for the combined two-year award period. NIH grants
policies as described in the NIH Grants Policy Statement will apply to the applications submitted and awards made
in response to this FOA.
All foreign applicants must complete and submit budget requests using the Research & Related Budget component.
F&A costs requested by consortium participants are not included in the direct cost limitation. See NOT-OD-05-004, November 2, 2004.
Section III. Eligibility Information
1.
Eligible Applicants
1.A.
Eligible Institutions
The following
organizations/institutions are eligible to apply:
1.B. Eligible Individuals
Any individual(s) with the skills, knowledge, and resources necessary to carry out the proposed research as the PD/PI is invited to work with his/her organization to develop an application for support. Individuals from underrepresented racial and ethnic groups as well as individuals with disabilities are always encouraged to apply for NIH support.
More than one PD/PI (i.e., multiple PDs/PIs), may be designated on the application for projects that require a “team science” approach and therefore clearly do not fit the single-PD/PI model. Additional information on the implementation plans and policies and procedures to formally allow more than one PD/PI on individual research projects is available at http://grants.nih.gov/grants/multi_pi. All PDs/PIs must be registered in the NIH electronic Research Administration (eRA) Commons prior to the submission of the application (see http://era.nih.gov/ElectronicReceipt/preparing.htm for instructions).
The decision of whether to apply for a grant with a single PD/PI or multiple PDs/PIs grant is the responsibility of the investigators and applicant organizations and should be determined by the scientific goals of the project. Applications for grants with multiple PDs/PIs will require additional information, as outlined in the instructions below. The NIH review criteria for approach, investigators, and environment have been modified to accommodate applications involving either a single PD/PI or multiple PDs/PIs. When considering the multiple PD/PI option, please be aware that the structure and governance of the PD/PI leadership team as well as the knowledge, skills and experience of the individual PDs/PIs will be factored into the assessment of the overall scientific merit of the application. Multiple PDs/PIs on a project share the authority and responsibility for leading and directing the project, intellectually and logistically. Each PD/PI is responsible and accountable to the grantee organization, or, as appropriate, to a collaborating organization, for the proper conduct of the project or program, including the submission of required reports. For further information on multiple PDs/PIs, please see http://grants.nih.gov/grants/multi_pi.
2. Cost Sharing or
Matching
This program does not require
cost sharing as defined in the current NIH
Grants Policy Statement.
3. Other-Special
Eligibility Criteria
Exploratory/developmental grant support is for new projects only; competing renewal (formerly “competing continuation”) applications will not be accepted.
Applicants may submit up to two resubmissions, but such application must include an Introduction addressing issues raised in the previous critique (Summary Statement). See NOT-OD-03-041, May 7, 2003.
Applicants may submit more than one application, provided each application is scientifically distinct.
Section IV. Application and Submission Information
To
download a SF424 (R&R) Application Package and SF424 (R&R) Application
Guide for completing the SF424 (R&R) forms for this FOA, use the “Apply for
Grant Electronically” button in this FOA or link to http://www.grants.gov/Apply/ and follow
the directions provided on that Web site.
A one-time registration is required for institutions/organizations at both:
PDs/PIs should work with their institutions/organizations to make sure they are registered in the NIH eRA Commons.
Several additional separate actions are required before an applicant can submit an electronic application, as follows:
1) Organizational/Institutional Registration in Grants.gov/Get Registered.
2) Organizational/Institutional Registration in the eRA Commons
3) Project Director/Principal Investigator (PD/PI) Registration in the NIH eRA Commons: Refer to the NIH eRA Commons System (COM) Users Guide.
Both the PD/PI and AOR/SO need separate accounts in the NIH eRA Commons since both are authorized to view the application image.
Note that if a PD/PI is also an NIH peer-reviewer with an Individual DUNS and CCR registration, that particular DUNS number and CCR registration are for the individual reviewer only. These are different than any DUNS number and CCR registration used by an applicant organization. Individual DUNS and CCR registration should be used only for the purposes of personal reimbursement and should not be used on any grant applications submitted to the Federal Government.
Several of the steps of the registration process could take four weeks or more. Therefore, applicants should immediately check with their business official to determine whether their organization/institution is already registered in both Grants.gov and the Commons. The NIH will accept electronic applications only from organizations that have completed all necessary registrations.
1. Request Application Information
Applicants must
download the SF424 (R&R) application forms and SF424 (R&R) Application
Guide for this FOA through Grants.gov/Apply.
Note:
Only the forms package directly attached to a specific FOA can be used. You
will not be able to use any other SF424 (R&R) forms (e.g., sample forms,
forms from another FOA), although some of the "Attachment" files may
be useable for more than one FOA.
For further assistance, contact GrantsInfo --
Telephone 301-435-0714, Email: GrantsInfo@nih.gov.
Telecommunications for the hearing impaired: TTY
301-451-0088.
2. Content and Form of Application Submission
Prepare all applications using the SF424 (R&R) application forms and in accordance with the SF424 (R&R) Application Guide (MS Word or PDF).
The SF424 (R&R) Application Guide is critical to submitting a complete and accurate application to NIH. There are fields within the SF424 (R&R) application components that, although not marked as mandatory, are required by NIH (e.g., the “Credential” log-in field of the “Research & Related Senior/Key Person Profile” component must contain the PD/PI’s assigned eRA Commons User ID). Agency-specific instructions for such fields are clearly identified in the Application Guide. For additional information, see “Frequently Asked Questions – Application Guide, Electronic Submission of Grant Applications.”
The SF424 (R&R) application is comprised of data arranged in separate components. Some components are required, others are optional. The forms package associated with this FOA in Grants.gov/APPLY will include all applicable components, required and optional. A completed application in response to this FOA will include the following components:
Required
Components:
SF424 (R&R) (Cover
component)
Research & Related Project/Performance Site
Locations
Research & Related Other Project Information
Research & Related Senior/Key Person
PHS398 Cover Page Supplement
PHS398 Research Plan
PHS398 Checklist
PHS398
Modular Budget or Research &
Related Budget,
as appropriate (See Section
IV.6., “Special Instructions,” regarding appropriate
required budget component.)
Optional Components:
PHS398 Cover Letter
File
Research & Related Subaward Budget Attachment(s)
Form
Foreign
Organizations (Non-domestic [non-U.S.] Entities)
NIH policies concerning
grants to foreign (non-U.S.) organizations can be found in the NIH Grants Policy Statement at: http://grants.nih.gov/grants/policy/nihgps_2003/NIHGPS_Part12.htm#_Toc54600260.
Applications from Foreign organizations must:
Proposed research should provide special opportunities for furthering research programs through the use of unusual talent, resources, populations, or environmental conditions in other countries that are not readily available in the United States (U.S.) or that augment existing U.S. resources.
SPECIAL INSTRUCTIONS
Applications with Multiple PDs/PIs
When multiple PDs/PIs are proposed, NIH requires one PD/PI to be designated as the "Contact” PI, who will be responsible for all communication between the PDs/PIs and the NIH, for assembling the application materials outlined below, and for coordinating progress reports for the project. The contact PD/PI must meet all eligibility requirements for PD/PI status in the same way as other PDs/PIs, but has no other special roles or responsibilities within the project team beyond those mentioned above.
Information for the Contact PD/PI should be entered in item 15 of the SF424 (R&R) Cover component. All other PDs/PIs should be listed in the Research & Related Senior/Key Person component and assigned the project role of “PD/PI.” Please remember that all PDs/PIs must be registered in the eRA Commons prior to application submission. The Commons ID of each PD/PI must be included in the “Credential” field of the Research & Related Senior/Key Person component. Failure to include this data field will cause the application to be rejected.
All projects proposing Multiple PDs/PIs will be required to include a new section describing the leadership plan approach for the proposed project.
Multiple PD/PI Leadership Plan: For applications designating multiple PDs/PIs, a new section of the research plan, entitled “Multiple PD/PI Leadership Plan” [Section 14 of the Research Plan Component in the SF424 (R&R)], must be included. A rationale for choosing a multiple PD/PI approach should be described. The governance and organizational structure of the leadership team and the research project should be described, and should include communication plans, process for making decisions on scientific direction, and procedures for resolving conflicts. The roles and administrative, technical, and scientific responsibilities for the project or program should be delineated for the PDs/PIs and other collaborators.
If budget allocation is planned, the distribution of resources to specific components of the project or the individual PDs/PIs should be delineated in the Leadership Plan. In the event of an award, the requested allocations may be reflected in a footnote on the Notice of Award (NoA).
Applications Involving a Single Institution
When all PDs/PIs are within a single institution, follow the instructions contained in the SF424 (R&R) Application Guide.
Applications Involving Multiple Institutions
When multiple institutions are involved, one institution must be designated as the prime institution and funding for the other institution(s) must be requested via a subcontract to be administered by the prime institution. When submitting a detailed budget, the prime institution should submit its budget using the Research & Related Budget component. All other institutions should have their individual budgets attached separately to the Research & Related Subaward Budget Attachment(s) Form. See Section 4.8 of the SF424 (R&R) Application Guide for further instruction regarding the use of the subaward budget form.
When submitting a modular budget, the prime institution completes the PHS398 Modular Budget component only. Information concerning the consortium/subcontract budget is provided in the budget justification. Separate budgets for each consortium/subcontract grantee are not required when using the Modular budget format. See Section 5.4 of the Application Guide for further instruction regarding the use of the PHS398 Modular Budget component.
3. Submission Dates and Times
See Section IV.3.A for details.
3.A. Submission, Review, and Anticipated Start Dates
Opening
Date: September 16, 2008 (Earliest date an application may be submitted to
Grants.gov)
Letter of Intent
Receipt Date(s): September 16, 2008
Application Due Date(s):
Standard dates apply, please see http://grants.nih.gov/grants/funding/submissionschedule.htm
AIDS Application Due Date(s): Standard dates apply,
please see http://grants1.nih.gov/grants/funding/submissionschedule.htm#AIDS
Peer Review
Date(s): Standard dates apply, please see http://grants1.nih.gov/grants/funding/submissionschedule.htm#reviewandaward
Council Review
Date(s): Standard dates apply, please see http://grants1.nih.gov/grants/funding/submissionschedule.htm#reviewandaward
Earliest
Anticipated Start Date(s): Standard dates apply, please see http://grants1.nih.gov/grants/funding/submissionschedule.htm#reviewandaward
3.A.1. Letter of Intent
Prospective applicants are asked to submit a letter of intent that includes the following information:
Although
a letter of intent is not required, is not binding, and does not enter into the
review of a subsequent application, the information that it contains allows IC
staff to estimate the potential review workload and plan the review.
The letter of intent is
to be sent by the date listed in Section IV.3.A.
The letter of intent
should be sent to:
Patricia
L. Mabry (Patty)
Health
Scientist Administrator/Behavioral Scientist
Office of
Behavioral and Social Sciences Research
Office of
the Director, NIH
31 Center
Drive, Building 31,
Room B1-C19; MSC 2027
Bethesda, MD 20892-2027
Phone:
(301) 402-1753
email: mabryp@od.nih.gov
3.B.
Submitting an Application Electronically to the NIH
To submit an application in
response to this FOA, applicants should access this FOA via http://www.grants.gov/Apply and follow
Steps 1-4. Note: Applications must only be submitted electronically.
PAPER APPLICATIONS WILL NOT BE ACCEPTED.
3.C. Application
Processing
Applications may be submitted on or after the opening date and must be successfully
received by Grants.gov no later than 5:00 p.m. local time (of the
applicant institution/organization) on the application due date(s). (See Section IV.3.A. for all dates.) If an application is not submitted
by the due date(s) and time, the application may be delayed in the review
process or not reviewed.
Once an application package has been successfully submitted through Grants.gov, any errors have been addressed, and the assembled application has been created in the eRA Commons, the PD/PI and the Authorized Organization Representative/Signing Official (AOR/SO) have two weekdays (Monday – Friday, excluding Federal holidays) to view the application image to determine if any further action is necessary.
Upon
receipt, applications will be evaluated for completeness by the Center for
Scientific Review, NIH. Incomplete applications will not be reviewed.
There will
be an acknowledgement of receipt of applications from Grants.gov and the Commons. The submitting AOR/SO
receives the Grants.gov acknowledgments. The AOR/SO and the PI receive Commons
acknowledgments. Information related to the assignment of an application to a
Scientific Review Group is also in the Commons.
Note: Since email can be unreliable, it is the responsibility of the applicant to check periodically on their application status in the Commons.
The NIH will not accept any application in response to this FOA that is essentially the same as one currently pending initial merit review unless the applicant withdraws the pending application. The NIH will not accept any application that is essentially the same as one already reviewed. However, the NIH will accept a resubmission application, but such application must include an Introduction addressing the critique from the previous review.
4.
Intergovernmental Review
This initiative is not
subject to intergovernmental
review.
5. Funding Restrictions
All NIH awards are
subject to the terms and conditions, cost principles, and other considerations
described in the NIH Grants
Policy Statement.
Pre-Award Costs are allowable. A grantee may, at
its own risk and without NIH prior approval, incur obligations and expenditures
to cover costs up to 90 days before the beginning date of the initial budget
period of a new award if such costs: are necessary to conduct the project, and
would be allowable under the grant, if awarded, without NIH prior approval. If
specific expenditures would otherwise require prior approval, the grantee must
obtain NIH approval before incurring the cost. NIH prior approval is required
for any costs to be incurred more than 90 days before the beginning date of the
initial budget period of a new award.
The incurrence of pre-award costs in anticipation of a
competing or non-competing award imposes no obligation on NIH either to make
the award or to increase the amount of the approved budget if an award is made
for less than the amount anticipated and is inadequate to cover the pre-award
costs incurred. NIH expects the grantee to be fully aware that pre-award costs
result in borrowing against future support and that such borrowing must not
impair the grantee's ability to accomplish the project objectives in the
approved time frame or in any way adversely affect the conduct of the project.
See the NIH
Grants Policy Statement.
All investigators are encouraged to attend
the annual grantee meeting for this FOA and consult their respective funding agencies to provide travel support when
necessary. Applicants to this FOA must allocate funds for at least two
key investigators with complementary expertise to travel to the annual grantee
meetings.
6. Other Submission
Requirements
PD/PI Credential
(e.g., Agency Login)
The NIH requires the PD/PI to fill in his/her Commons User ID in the “PROFILE – Project Director/Principal Investigator” section, “Credential” log-in field of the “Research & Related Senior/Key Person Profile” component. The applicant organization must include its DUNS number in its Organization Profile in the eRA Commons. This DUNS number must match the DUNS number provided at CCR registration with Grants.gov. For additional information, see “Registration FAQs – Important Tips -- Electronic Submission of Grant Applications.”
Organizational DUNS
The applicant organization must include its DUNS number in its Organization Profile in the eRA Commons. This DUNS number must match the DUNS number provided at CCR registration with Grants.gov. For additional information, see “Frequently Asked Questions – Application Guide, Electronic Submission of Grant Applications.”
PHS398 Research Plan Component Sections
While each section of the Research Plan component needs to be uploaded separately as a PDF attachment, applicants are encouraged to construct the Research Plan component as a single document, separating sections into distinct PDF attachments just before uploading the files. This approach will enable applicants to better monitor formatting requirements such as page limits. All attachments must be provided to NIH in PDF format, filenames must be included with no spaces or special characters, and a .pdf extension must be used.
All application instructions outlined in the SF424 (R&R) Application Guide are to be followed, incorporating "Just-in-Time" information concepts, and with the following requirements for R21 applications:
Appendix Materials
Applicants must follow the specific instructions on Appendix materials as described in the SF424 (R&R) Application Guide (See http://grants.nih.gov/grants/funding/424/index.htm). Also see http://grants.nih.gov/grants/guide/notice-files/NOT-OD-07-018.html.
Do not use the Appendix to circumvent the page limitations of the Research Plan component. An application that does not comply with these limitations may be delayed in the review process.
Resource Sharing Plan(s)NIH considers the sharing of unique research resources developed through NIH-sponsored research an important means to enhance the value and further the advancement of the research. When resources have been developed with NIH funds and the associated research findings published or provided to NIH, it is important that they be made readily available for research purposes to qualified individuals within the scientific community. If the final data/resources are not amenable to sharing, this must be explained in the Resource Sharing section of the application (see http://grants.nih.gov/grants/policy/data_sharing/data_sharing_faqs.htm.)
(a) Data Sharing Plan: Investigators seeking $500,000 or more in direct costs in any year are expected to include a brief 1-paragraph description of how final research data will be shared, or explain why data-sharing is not possible. Applicants are encouraged to discuss data-sharing plans with their NIH program contact (see Data-Sharing Policy or http://grants.nih.gov/grants/guide/notice-files/NOT-OD-03-032.html.)
The adequacy of the resources sharing plan and any related data sharing plans will be considered by Program staff of the funding organization when making recommendations about funding applications. The effectiveness of the resource sharing will be evaluated as part of the administrative review of each Non-Competing Grant Progress Report (PHS 2590). See Section VI.3., “Reporting.”
Foreign Applications (Non-domestic [non-U.S.] Entities)
Indicate how the proposed project has specific relevance to the mission and objectives of the NIH/IC and has the potential for significantly advancing the health sciences in the United States
Section V. Application Review Information
1. Criteria
Only the review criteria described below will be considered in the review process.
2. Review and
Selection Process
Applications submitted for this funding opportunity
will be assigned to the ICs on the basis of established Public Health Service (PHS) referral guidelines.
Applications
that are complete will be evaluated for scientific and technical merit by an
appropriate peer review group convened by the
Center for Scientific Review (CSR) and in accordance with NIH peer
review procedures (http://grants1.nih.gov/grants/peer/),
using the review criteria stated below.
As part of the initial merit review, all applications will:
Applications submitted in response to this funding opportunity will compete for available funds with all other recommended applications
The following will be considered in making funding decisions:
The NIH R21 exploratory/developmental grant is a mechanism for supporting novel scientific ideas or new model systems, tools, or technologies that have the potential to significantly advance our knowledge or the status of health-related research.
Because the Research Plan component is limited to 15 pages, an exploratory/developmental grant application need not have extensive background material or preliminary information as one might normally expect in an R01 application. Accordingly, reviewers will focus their evaluation on the conceptual framework, the level of innovation, and the potential to significantly advance our knowledge or understanding. Reviewers will place less emphasis on methodological details and certain indicators traditionally used in evaluating the scientific merit of R01 applications, including supportive preliminary data. Appropriate justification for the proposed work can be provided through literature citations, data from other sources, or, when available, from investigator-generated data. Preliminary data are not required for R21 applications; however, they may be included if available.
The goals of NIH supported research are to advance our understanding of biological systems, to improve the control of disease, and to enhance health. In their written critiques, reviewers will be asked to comment on each of the following criteria in order to judge the likelihood that the proposed research will have a substantial impact on the pursuit of these goals. Each of these criteria will be addressed and considered in assigning the overall score, weighting them as appropriate for each application.
Note that an application does not need to be strong in
all categories to be judged likely to have major scientific impact and thus
deserve a meritorious priority score. For example, an investigator may propose
to carry out important work that by its nature is not innovative but is
essential to move a field forward.
Significance: Does this study address an
important problem? If the aims of the application are achieved, how will
scientific knowledge or clinical practice be advanced? What will be the effect
of these studies on the concepts, methods, technologies, treatments, services,
or preventative interventions that drive this field?
Will the results of the project be able to inform public health practitioners an d other relevant parties regarding decisions relevant to the policy resistant problem under study?
Approach: Are the conceptual or clinical framework, design, methods, and analyses adequately developed, well-integrated, well-reasoned, and appropriate to the aims of the project? Does the applicant acknowledge potential problem areas and consider alternative tactics? For applications designating multiple PDs/PIs, is the leadership approach, including the designated roles and responsibilities, governance, and organizational structure, consistent with and justified by the aims of the project and the expertise of each of the PDs/PIs? Is the primary approach one that is centered in systems science methodology? Is the subject of the study a policy resistant problem? Does the approach incorporate behavioral and social factors that influence health?
Innovation: Is the project original and innovative? For example: Does the project challenge existing paradigms or clinical practice; address an innovative hypothesis or critical barrier to progress in the field? Does the project develop or employ novel concepts, approaches or methodologies, tools, or technologies for this area?
Investigators: Are the PD/PIs and other key personnel appropriately trained and well suited to carry out this work? Is the work proposed appropriate to the experience level(s) of the principal investigator(s) and other researchers? Do the PD/PIs and investigative team bring complementary and integrated expertise to the project (if applicable)? Does the investigative team include members with expertise in syst ems science methodology as well as those with health and medical expertise in the appropriate content area for the problem under study ?
Environment: Do(es) the scientific environment(s) in which the work will be done contribute to the probability of success? Do the proposed studies benefit from unique features of the scientific environment(s), or subject populations, or employ useful collaborative arrangements? Is there evidence of institutional support?
2.A. Additional Review Criteria:
In addition to the above criteria, the following items will continue to be considered in the determination of scientific merit and the rating:
Resubmission Applications: Are the responses to
comments from the previous scientific review group adequate? Are the
improvements in the resubmission application appropriate?
Protection of
Human Subjects from Research Risk: The involvement of human subjects and protections
from research risk relating to their participation in the proposed research
will be assessed. See item 6 of the Research Plan component of the SF424
(R&R).
Inclusion of Women, Minorities and Children in Research: The adequacy of
plans to include subjects from both genders, all racial and ethnic groups (and
subgroups), and children as appropriate for the scientific goals of the research
will be assessed. Plans for the recruitment and retention of subjects will also
be evaluated. See item 7 of the Research Plan component of the SF424
(R&R).
Care and Use of Vertebrate Animals in Research: If vertebrate animals
are to be used in the project, the five items described under item 11 of the
Research Plan component of the SF424 (R&R) will be assessed.
Biohazards: If materials or procedures are proposed that are potentially
hazardous to research personnel and/or the environment, determine if the
proposed protection is adequate.
2.B.
Additional Review Considerations
Budget and Period of Support: The
reasonableness of the proposed budget and the requested period of support in
relation to the proposed research. The priority score should not be affected by
the evaluation of the budget.
Applications from Foreign Organizations: Whether the project presents special opportunities for furthering research programs through the use of unusual talent, resources, populations, or environmental conditions in other countries that are not readily available in the United States or that augment existing U.S. resources will be assessed
2.C. Resource Sharing Plan(s)When relevant, reviewers will be instructed to comment on the reasonableness of the following Resource Sharing Plans, or the rationale for not sharing the following types of resources. However, reviewers will not factor the proposed resource sharing plan(s) into the determination of scientific merit or priority score, unless noted otherwise in the FOA. Program staff within the IC will be responsible for monitoring the resource sharing.
3.
Anticipated Announcement and Award Dates
Not Applicable
Section VI. Award Administration Information
1.
Award Notices
After the peer review of the application is
completed, the PD/PI will be able to access his/her Summary Statement (written
critique) via the NIH eRA Commons.
If
the application is under consideration for funding, NIH will request
"just-in-time" information from the applicant. For details,
applicants may refer to the NIH
Grants Policy Statement Part II: Terms and Conditions of NIH Grant Awards,
Subpart A: General.
A formal notification in the form of a Notice of Award
(NoA) will be provided to the applicant organization. The NoA signed by the
grants management officer is the authorizing document. Once all administrative and
programmatic issues have been resolved, the NoA will be generated via email
notification from the awarding component to the grantee business official.