Opportunity Information: Apply for PA 14 334
Apply for PA 14 334
- The National Institutes of Health in the education food and nutrition health sector is offering a public funding opportunity titled "Advancing Interventions to Improve Medication Adherence (R01)" and is now available to receive applicants.
- Interested and eligible applicants and submit their applications by referencing the CFDA number(s): 93.173 Research Related to Deafness and Communication Disorders 93.213 Research and Training in Complementary and Integrative Health 93.242 Mental Health Research Grants 93.273 Alcohol Research Programs 93.361 Nursing Research 93.393 Cancer Cause and Prevention Research 93.395 Cancer Treatment Research 93.399 Cancer Control 93.837 Cardiovascular Diseases Research 93.847 Diabetes, Digestive, and Kidney Diseases Extramural Research 93.867 Vision Research.
- This funding opportunity was created on Sep 5, 2014 and posted on Sep 4, 2014.
- Applicants must submit their applications by Jan 7, 2018. (Agency may still review applications by suitable applicants for the remaining/unused allocated funding in 2026.)
- Eligible applicants include: Special district governments Small businesses Independent school districts City or township governments Nonprofits that do not have a 501(c)(3) status with the IRS, other than institutions of higher education For profit organizations other than small businesses State governments Private institutions of higher education Public and State controlled institutions of higher education Public housing authorities/Indian housing authorities Others (see text field entitled Additional Information on Eligibility for clarification) County governments Native American tribal governments (Federally recognized) Nonprofits having a 501(c)(3) status with the IRS, other than institutions of higher education Native American tribal organizations (other than Federally recognized tribal governments).
- Other Eligible Applicants include the following Alaska Native and Native Hawaiian Serving Institutions Asian American Native American Pacific Islander Serving Institutions (AANAPISISs) Eligible Agencies of the Federal Government Faith based or Community based Organizations Hispanic serving Institutions Historically Black Colleges and Universities (HBCUs) Indian/Native American Tribal Governments (Other than Federally Recognized) Non domestic (non U.S.) Entities (Foreign Organizations) Regional Organizations Tribally Controlled Colleges and Universities (TCCUs) U.S. Territory or Possession Non domestic (non U.S.) Entities (Foreign Institutions) are not eligible to apply. Non domestic (non U.S.) components of U.S. Organizations are not eligible to apply. Foreign components, as defined in the NIH Grants Policy Statement, are not allowed.
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Opportunity Summary:
The NIH funding opportunity titled "Advancing Interventions to Improve Medication Adherence (R01)" (Funding Opportunity Number PA-14-334) supports Research Project Grant (R01) applications focused on designing and testing interventions that can meaningfully increase how well people take their prescribed medications. The program is coordinated through the NIH Adherence Network and led by the Office of Behavioral and Social Sciences Research (OBSSR), with participation from multiple NIH Institutes and Centers. The central emphasis is on intervention research with a clear plan to move the needle on adherence in real people, rather than purely descriptive work on why nonadherence happens.
Projects may focus on adherence for a single disease or chronic condition, such as hypertension, where consistent medication use is critical for controlling blood pressure and preventing downstream complications. They may also address adherence intended to prevent recurrence or progression, such as long-term therapies in cancer survivorship. The FOA also explicitly allows and encourages applications targeting people managing multiple comorbid conditions, recognizing that polypharmacy, competing health demands, and overlapping behavioral and social barriers can make adherence especially challenging in populations dealing with combinations such as hypertension, diabetes, alcohol use disorders, and HIV/AIDS. In other words, applicants are not limited to one therapeutic area; the unifying requirement is that the proposed work centers on improving medication-taking behavior in a way that is likely to produce measurable health benefits.
A strong, well-articulated theoretical or conceptual framework is presented as a key expectation for responsive applications. This means proposals should do more than list intervention components; they should explain why those components should work, grounded in an established behavioral, social, clinical, or implementation-oriented model. Reviewers are being signaled to look for a coherent logic model connecting determinants of adherence (for example, beliefs about medication, habits, side effects, access barriers, regimen complexity, mental health, substance use, health literacy, clinician-patient communication, or structural constraints) to specific intervention strategies and to anticipated improvements in adherence and health outcomes.
On measurement, the FOA makes it clear that self-report alone is not sufficient. While patient-reported adherence can be included as a primary outcome, each study must also incorporate at least one non-self-report measure of adherence. Examples provided include pharmacy refill records and electronic monitoring, but the intent is broader: the research design should include an objective or externally verifiable adherence indicator that strengthens confidence in the findings. Beyond adherence metrics, applicants are encouraged to include a relevant health outcome or biomarker expected to change if adherence improves. The FOA lists examples such as blood pressure for antihypertensive therapy, HIV viral load for antiretroviral adherence, cholesterol levels for lipid-lowering medications, and HbA1c for diabetes management. For conditions without a well-established biomarker, the announcement notes that a clinical assessment can fill this role, such as medication blood levels, structured diagnostic interviews, or independent clinician ratings of symptoms and behaviors. The through-line here is that NIH wants adherence outcomes linked to clinically meaningful endpoints, not adherence measured in isolation.
Administratively, this is a discretionary grant opportunity using the NIH R01 mechanism. It was posted in September 2014, with the final listed closing date in January 2018 and an archive date in February 2018, indicating the specific announcement is no longer active, though similar NIH adherence-focused opportunities may exist under newer FOAs. No cost sharing or matching is required. The activity category is listed broadly under education, food and nutrition, and health, and the opportunity is connected to multiple CFDA program areas spanning communication disorders, complementary and integrative health, mental health, alcohol research, nursing research, cancer prevention and treatment, cardiovascular disease, diabetes and kidney diseases, and vision research. This cross-cutting footprint reflects that medication adherence is a common bottleneck across many diseases and care settings.
Eligibility is broad and includes many types of domestic organizations and governments, such as public and private institutions of higher education, nonprofit organizations (including 501(c)(3) and certain non-501(c)(3) entities), for-profit organizations (including small businesses and other for-profits), independent school districts, and a range of state, county, city/township, special district, and tribal governments. The FOA also calls out additional eligible applicants such as Historically Black Colleges and Universities (HBCUs), Hispanic-serving institutions, tribally controlled colleges and universities, Alaska Native and Native Hawaiian serving institutions, and faith-based or community-based organizations, among others. At the same time, it restricts foreign involvement: non-U.S. entities and foreign institutions are not eligible to apply, non-domestic components of U.S. organizations are not eligible, and foreign components as defined by NIH policy are not allowed. This means applicants need to plan for a fully domestic project footprint under NIH definitions.
In practical terms, the opportunity is aimed at teams that can design a theoretically grounded adherence intervention, implement it with rigorous methods, and evaluate it using both objective adherence measures and clinically relevant outcomes. Successful proposals under this FOA would typically be expected to show a tight alignment among the targeted population and condition(s), the barriers the intervention is meant to address, the mechanism by which the intervention will change adherence behavior, and a measurement plan that can demonstrate not only improved adherence but also downstream improvements in health indicators that matter to patients and clinicians.
Frequently Asked Questions (FAQs)
What is the name of this NIH funding opportunity?
The funding opportunity is titled "Advancing Interventions to Improve Medication Adherence (R01)" and carries Funding Opportunity Number (FON) PA-14-334.
What type of grant mechanism does this opportunity use?
It uses the NIH Research Project Grant (R01) mechanism.
What is the main purpose of PA-14-334?
The opportunity supports R01 research projects that design and test interventions intended to meaningfully improve how well people take prescribed medications (medication adherence), with an emphasis on measurable improvements in real-world adherence behavior.
Is the focus on understanding why nonadherence happens, or on changing adherence?
The central emphasis is on intervention research that aims to improve adherence, not purely descriptive research focused only on explaining reasons for nonadherence.
Who coordinates and leads this program at NIH?
The program is coordinated through the NIH Adherence Network and led by the Office of Behavioral and Social Sciences Research (OBSSR), with participation from multiple NIH Institutes and Centers.
What kinds of diseases or conditions can be addressed?
Projects may focus on medication adherence in a single disease or chronic condition (for example, hypertension) or in settings where adherence helps prevent recurrence or progression (for example, long-term therapies in cancer survivorship). The opportunity is not limited to one therapeutic area as long as the work centers on improving medication-taking behavior and is likely to yield measurable health benefits.
Are projects focused on people with multiple chronic conditions allowed?
Yes. The FOA explicitly allows and encourages applications that target individuals managing multiple comorbid conditions, acknowledging challenges such as polypharmacy, competing health demands, and overlapping behavioral and social barriers.
Does the FOA provide examples of comorbid combinations that may be relevant?
Yes. It notes combinations such as hypertension, diabetes, alcohol use disorders, and HIV/AIDS as examples of overlapping conditions where adherence can be especially challenging.
What does NIH expect regarding theory or conceptual framework?
Responsive applications are expected to present a strong, well-articulated theoretical or conceptual framework. The proposal should clearly explain why the intervention components should work, grounded in an established behavioral, social, clinical, or implementation-oriented model.
What is meant by a "logic model" in the context of this FOA?
The FOA signals that reviewers will look for a coherent logic model that links determinants of adherence to specific intervention strategies and then to expected improvements in adherence and health outcomes.
What kinds of adherence determinants or barriers are considered relevant?
The FOA provides examples such as beliefs about medication, habits, side effects, access barriers, regimen complexity, mental health, substance use, health literacy, clinician-patient communication, and structural constraints.
What are the measurement requirements for adherence outcomes?
Self-report alone is not sufficient. While patient-reported adherence can be included (including as a primary outcome), each study must also include at least one non-self-report (objective or externally verifiable) measure of adherence.
What are examples of non-self-report adherence measures mentioned in the FOA?
Examples provided include pharmacy refill records and electronic monitoring.
Does the FOA require measuring health outcomes in addition to adherence?
Applicants are encouraged to include a relevant health outcome or biomarker that would be expected to change if adherence improves, linking adherence changes to clinically meaningful endpoints.
What are examples of health outcomes or biomarkers linked to adherence that are mentioned?
The FOA lists examples such as blood pressure (for antihypertensive therapy), HIV viral load (for antiretroviral adherence), cholesterol levels (for lipid-lowering medications), and HbA1c (for diabetes management).
What if a condition does not have a well-established biomarker?
The FOA notes that a clinical assessment can fill this role, such as medication blood levels, structured diagnostic interviews, or independent clinician ratings of symptoms and behaviors.
Is cost sharing or matching required?
No. The opportunity states that no cost sharing or matching is required.
Is PA-14-334 still an active funding opportunity?
No. It was posted in September 2014, with a final listed closing date in January 2018 and an archive date in February 2018, indicating that this specific announcement is no longer active (though similar NIH opportunities may exist under newer FOAs).
What is the broad activity category associated with this opportunity?
The activity category is listed broadly under education, food and nutrition, and health.
Which NIH/CFDA-related program areas are associated with this FOA?
The opportunity is connected to multiple program areas spanning communication disorders, complementary and integrative health, mental health, alcohol research, nursing research, cancer prevention and treatment, cardiovascular disease, diabetes and kidney diseases, and vision research.
What types of organizations are eligible to apply?
Eligibility is broad and includes many types of domestic organizations and governments, such as public and private institutions of higher education, nonprofit organizations (including 501(c)(3) and certain non-501(c)(3) entities), for-profit organizations (including small businesses and other for-profits), independent school districts, and various state, county, city/township, special district, and tribal governments.
Are minority-serving and community-based institutions explicitly included as eligible applicants?
Yes. The FOA calls out additional eligible applicants such as Historically Black Colleges and Universities (HBCUs), Hispanic-serving institutions, tribally controlled colleges and universities, Alaska Native and Native Hawaiian serving institutions, and faith-based or community-based organizations, among others.
Are foreign organizations eligible to apply?
No. Non-U.S. entities and foreign institutions are not eligible to apply.
Can a U.S. organization include a non-U.S. (non-domestic) component under this FOA?
No. Non-domestic components of U.S. organizations are not eligible.
Are foreign components allowed in any form?
No. Foreign components as defined by NIH policy are not allowed under this FOA.
What does a "fully domestic project footprint" mean in practical terms for this FOA?
Based on the stated restrictions, applicants must plan for the project to be carried out entirely within the United States under NIH definitions, without foreign institutions, non-domestic organizational components, or NIH-defined foreign components.
What would a strong proposal look like, based on the FOA's emphasis?
A strong application would typically show tight alignment among (1) the targeted population and condition(s), (2) the specific barriers to adherence being addressed, (3) a theory-driven mechanism explaining how the intervention will change medication-taking behavior, and (4) a rigorous measurement plan that includes at least one objective adherence measure and ties adherence improvements to clinically meaningful health indicators.
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