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The U.S. Agency for International Development (USAID) invites interested Nigerian entities to participate in a pre-application conference for integrated Delivery of TB Services (iDOTS) Activity to be held on July 30, 2024 in Abuja. The purpose of the USAID/Nigeria integrated Delivery of TB Services (iDOTS) Activity is to reach every person with TB, cure those in need of treatment, prevent new infections and progression to active disease, while scaling-up innovations in detection, care, and treatment, and fostering local ownership to sustain TB programs that contribute to integrated primary health care services and pandemic preparedness in supported states.

The mission of the Arizona Department of Health Services (ADHS) Arizona Biomedical Research Centre (ABRC) is to identify and support innovative biomedical research to improve the health of all Arizonans. ABRC is focused on leveraging existing resources, maximizing partnerships, cultivating communication, and promoting innovation. ABRC manages multiple initiatives which are guided by input from leaders and professionals from Arizona’s universities, nonprofit research institutions, hospitals, medical centers, and patient advocacy groups. Financial Notes: Funding Source: The funding source for this Grant is the Health Research Fund (Tobacco Tax) as established by Arizona Revised Statute (ARS) §36-275 (https://www.azleg.gov/ars/36/00275.htm) and §36-773  (https://www.azleg.gov/ars/36/00773.htm). Up to $3,500,000 per year is available for Arizona Investigator Grant (AZ IG) and New Investigator Award (NIA) applications. The maximum award for AZ IG Applications is $225,000.00 annually with a maximum project duration of three (3) years from the award date. The maximum award for NIA Applications is $75,000.00 annually with a maximum project duration of three (3) years from the award date.

The USAID THRIVE activity aims to contribute to achieving sustained epidemic control by improving the health and wellbeing of children living with HIV and reducing the risk of HIV infection among vulnerable children, adolescents, and caregivers. The activity will provide a suite of comprehensive services to build resilience and mitigate the multiple, layered vulnerabilities faced by these sub-populations. The target population for THRIVE activity is children and adolescents living with HIV (CALHIV), children whose caregivers are living with HIV (CPLHIV), HIV exposed infants (HEI), children of key populations (CKP), survivors of sexual violence against children (SVAC), and high-risk adolescent boys and girls, including out of school children.

The FY24 PCRP Early Investigator Research Award supports prostate cancer-focused research opportunities for individuals in the early stages of their careers under the guidance of one or more designated mentors. This opportunity allows early-career investigators to develop a research project, investigate a problem or question in prostate cancer research, and further their intellectual development as prostate cancer researchers of the future. All application components for the FY24 PCRP Early Investigator Research Award are to be written by the Principal Investigator (PI), with appropriate direction from the mentor(s).Key elements of this award mechanism are as follows: Principal Investigator: The postdoctoral investigator is considered the PI of the application and must exhibit strong potential for and commitment to pursuing a career as an investigator at the forefront of prostate cancer research; however, the PI is not required to have previous prostate cancer research experience. The PI must have 3 years or less of postdoctoral research experience (excluding clinical residency or clinical fellowship training) as of March 31, 2025. The PCRP strongly encourages applications from PIs who demonstrate a commitment to pursuing a career focused on prostate cancer health disparity research. Mentor(s): Applications must include at least one mentor appropriate to the proposed research project who has experience in prostate cancer research and mentoring as demonstrated by a record of active funding, recent publications, and successful mentorship. The primary mentor can be a junior faculty member, in which case the PI is encouraged to include a secondary mentor with a more robust track record in prostate cancer research and mentorship. Applications that focus on prostate cancer health disparity should include at least one mentor with experience in prostate cancer health disparity research. The selected mentor(s) should also demonstrate a clear commitment to the development of the PI toward independence as a prostate cancer researcher. Research Approach: Proposed research ideas are required to address one or more of the FY24 PCRP Overarching Challenges. Projects that specifically address the FY24 PCRP Overarching Challenge to advance health equity and reduce disparities in prostate cancer are strongly encouraged. The scientific rationale and experimental methodology should demonstrate in-depth analysis of the research problem presented. The feasibility of the research design and methods should be well defined, and a clear plan should be articulated as to how the proposed goals of the project can be achieved. Inclusion of preliminary data relevant to prostate cancer and the proposed project is encouraged but not required. Any preliminary data provided should be from the PI, mentor(s), or member(s) of the collaborating team. Additionally, required resources should be identified and supported through documentation. Research involving human subjects and human anatomical substances is permitted; however, clinical trials are not allowed under this funding opportunity. Researcher Development Plan: The PI must outline an individualized, prostate cancer-focused researcher development plan, which should include a clearly articulated strategy for acquiring the necessary skills, competence, and expertise that will enable the PI to successfully complete the proposed research project and foster the PIs development as an independent prostate cancer researcher. An environment appropriate to the proposed mentoring and research project must be clearly described, although any deficiencies of resources and/or mentorship at the PIs institution can be mitigated through collaboration(s) with other institutions. If the PI will be utilizing resources at another institution to successfully complete the proposed project, then the PI is strongly encouraged to designate a co-mentor at the collaborating institution.Investigators are strongly encouraged to incorporate the following components into their study design, where appropriate, in order to maximize the potential impact of the proposed research project: authentication of proposed cell lines; statistical rigor of preclinical animal experiments; and incorporation of experiments to assess clinical relevance and translatability of findings. Studies utilizing data derived from large patient studies that include long-term health records, biospecimen repositories, and pre-existing research and apply state-of-the-art genomic and/or proteomic analysis, bioinformatics, and/or mathematical models to such data are also encouraged. Investigators are highly encouraged to provide a letter of support indicating access to and the availability of any resources required to support the study.A congressionally mandated Metastatic Cancer Task Force was formed with the purpose of identifying ways to help accelerate clinical and translational research aimed at extending the lives of advanced state and recurrent patients. As a member of the Metastatic Cancer Task Force, the CDMRP encourages applicants to review the recommendations (https://health.mil/Reference-Center/Congressional-Testimonies/2018/05/03/Metastatic-Cancer-Research) and submit research ideas to address these recommendations provided they are within the limitations of this funding opportunity and fit within the FY24 PCRP priorities.Innovative research involving nuclear medicine and related techniques to support early diagnosis, more-effective treatment, and improved health outcomes of active-duty Service Members and their Families is encouraged. Such research could improve diagnostic and targeted treatment capabilities through noninvasive techniques and may drive the development of precision imaging and advanced targeted therapies.Applications from investigators within the military services and applications involving multidisciplinary collaborations among academia, industry, the military services, the U.S. Department of Veterans Affairs (VA), and other federal government agencies are highly encouraged. These relationships can leverage knowledge, infrastructure, and access to unique clinical populations that the collaborators bring to the research effort, ultimately advancing research that is of significance to Service Members, Veterans, and/or their Families. If the proposed research relies on access to unique resources or databases, the application must describe the access at the time of submission and include a plan for maintaining access as needed throughout the proposed research.All projects should adhere to a core set of standards for rigorous study design and reporting to maximize the reproducibility and translational potential of clinical and preclinical research. The standards are described in SC Landis et al., 2012, A call for transparent reporting to optimize the predictive value of preclinical research, Nature 490:187-191 (http://www.nature.com/nature/journal/v490/n7419/full/nature11556.html). While these standards are written for preclinical studies, the basic principles of randomization, blinding, sample-size estimation, and data handling derive from well-established best practices in clinical studies.Clinical trials are not allowed. A clinical trial is defined in the Code of Federal Regulations, Title 45, Part 46.102 (45 CFR 46.102) as a research study in which one or more human subjects are prospectively assigned to one or more interventions (which may include a placebo or another control) to evaluate the effects of the interventions on biomedical or behavioral health-related outcomes.Studies that do not seek to measure safety, effectiveness, and/or efficacy outcome(s) of an intervention are not considered clinical trials.For the purposes of this funding opportunity, research that meets the definition of a clinical trial is distinct from clinical research. Clinical research encompasses research with human data, human specimens, and/or interaction with human subjects. Clinical research is observational in nature and includes:(1) Research conducted with human subjects and/or material of human origin such as data, specimens, and cognitive phenomena for which an investigator (or co-investigator) does not seek to assess the safety, effectiveness, and/or efficacy outcomes of an intervention. Research meeting this definition may include but is not limited to: (a) mechanisms of human disease, (b) diagnostic or detection studies (e.g., biomarker or imaging), (c) health disparity studies, and (d) development of new technologies.(2) Epidemiologic and behavioral studies that do not seek to assess the safety, effectiveness, and/or efficacy outcomes of an intervention.(3) Outcomes research and health services research that do not fit under the definition of clinical trial.Excluded from the definition of clinical research are in vitro studies that utilize human data or specimens that cannot be linked to a living individual and meet the requirements for exemption under 46.104(d)(4) of the Common Rule.The funding instrument for awards made under the program announcement will be grants (31 USC 6304).The anticipated direct costs budgeted for the entire period of performance for an FY24 PCRP Early Investigator Research Award should not exceed $300,000. Refer to Section II.D.5, Funding Restrictions, for detailed funding information.Awards supported with FY24 funds will be made no later than September 30, 2025.The CDMRP expects to allot approximately $6.24M to fund approximately 13 Early Investigator Research Award applications. Funding of applications received is contingent upon the availability of federal funds for this program, the number of applications received, the quality and merit of the applications as evaluated by peer and programmatic review, and the requirements of the government. Funds to be obligated on any award resulting from this funding opportunity will be available for use for a limited time period based on the fiscal year of the funds. It is anticipated that awards made from this FY24 funding opportunity will be funded with FY24 funds, which will expire for use on September 30, 2030.

The United States Government, represented by the United States Agency for International Development (USAID) at its Mission in Southern Africa through the Bilateral Health Office (BHO) is publishing this Request for Information to obtain information and input from all interested entities, U.S. and non-U.S. organizations, on a potential future HIV Prevention among Adolescent Girls and Young Women and Other Vulnerable Youth Populations (North) Activity (also referred to as DREAMS North) and or HIV Prevention among Adolescent Girls and Young Women and Other Vulnerable Youth Populations (South) Activity (also referred to as DREAMS South). The information will be used to help make planning decisions and may inform activity design to improve future development outcomes. This Request for Information (RFI) is issued solely for information gathering purposes and is published inaccordance with FAR Part 10 and FAR 15.201(e).

The Parks & Public Space Initiative, supported by the Oklahoma City Community Foundation, focuses on enhancing public lands within the Greater Oklahoma City area. This initiative stems from the Margaret Annis Boys Trust, established in 1991, with a mission to encourage landscaping and beautification projects in public spaces such as parks, medians, and other public lands. The foundation's strategic priority is to foster community engagement and improve the quality of public spaces for residents, aligning with a theory of change that posits improved public spaces lead to increased community well-being and utilization. The target beneficiaries of this grant program include neighborhood/community groups, 501(c)(3) nonprofit organizations, and local government agencies within Oklahoma County that are connected to parks, school parks, trails, and other public spaces. The program aims to achieve several impact goals: increasing the utilization of public spaces for recreation, cultural, and health improvement; engaging various community entities in improving these spaces and their programs; and enhancing community stewardship of parks, school parks, trails, and other public lands. The initiative prioritizes funding landscaping and beautification projects in public community spaces, including neighborhood/community parks, school parks, trails, public medians, and other public lands in central Oklahoma. Eligible items for funding include plant materials, soil amendments, mulch, irrigation, and landscape amenities like shade structures and benches. Master plans and tree canopy studies are also considered. While the majority of grants support infrastructure and related activities, neighborhood streetscapes are a lower priority. Projects must be completed within one year and be open and accessible to the public. Expected outcomes and measurable results include a demonstrable increase in the use of public spaces, improved aesthetic quality of parks and public lands, and stronger community involvement in the planning, implementation, and ongoing maintenance of these projects. A significant volunteer component is required for each proposal, underscoring the program's commitment to fostering community stewardship. Additionally, a realistic location, installation, and maintenance plan with identified responsibilities and budget must be submitted to ensure the project’s sustainability, with tree plantings specifically requiring a three-year maintenance plan for establishment.

Le maintien en vie des personnes vivant avec le VIH (PVVIH) sous traitement antirtroviral (ARV) reste un dfi pour atteindre les objectifs 95-95-95 de l'ONUSIDA.L'initiative de Suivi Communautaire/The Community-Led Monitoring (CLM) vise aider les programmes et les tablissements du Plan d'urgence du Prsident des tats-Unis d'Amrique pour la lutte contre le SIDA (U.S. President's Emergency Plan for AIDS Relief PEPFAR) s'assurer qu'ils fournissent des services de qualit que les bnficiaires souhaitent utiliser en collaboration avec les organisations communautaires et leurs pairs navigateurs. La collaboration avec les groupes communautaires, les organisations de la socit civile et les patients/bnficiaires peut aider les programmes de lutte contre le VIH et les institutions de sant identifier les obstacles et les leviers pour faciliter l'accs et l'utilisation des services de lutte contre le VIH et amliorer la rtention.

With this solicitation, OJJDP seeks applications for funding to support cross-system collaboration to improve responses and outcomes for youth under the age of 18 or youth under the jurisdiction of the juvenile justice system with mental health disorders (MHD) or co-occurring mental health and substance use disorders (MHSUDs) who come in contact with the juvenile justice system. This program supports public safety efforts through partnerships with youth justice, mental health, and substance use agencies to enhance responses to justice-involved youth with MHD and MHSUDs.

The U.S. Embassy Addis Ababa /PEPFAR Ethiopia Coordination Office the U.S. Department of State announces an open competition for organizations to submit applications to carry out PEPFAR Community Led Monitoring Program. The primary goal of the Community Led Monitoring (CLM) program is to assist healthcare institutions and providers in identifying and addressing emerging or persistent issues, challenges, and barriers related to the delivery, uptake, and accessibility of HIV services at community and facility levels. Through continuous monitoring and advocacy efforts, CLM aims to enhance the quality-of-service delivery and improve client outcomes by identifying data driven solutions that can overcome obstacles and ensure beneficiaries have access to and receive optimal client-centered HIV services. The CLM initiative plays a crucial role in ensuring the availability, accessibility, and delivery of high-quality HIV care and services. By empowering clients and communities to actively seek out information, enhancing their health literacy, promoting engagement with health service delivery, supporting demand creation, advocacy for necessary change and demanding accountability from the health system, CLM aims to improve the overall quality of these services. The CLM initiative is a vital component in the ongoing efforts to address HIV-related challenges and improve the delivery of client centered HIV services. By leveraging data-driven solutions and fostering community engagement, CLM aims to enhance the quality of care and support provided to individuals affected by HIV and sustain the response. Participants and Audiences: The PEPFAR Coordination Office is currently inviting proposals from registered local or national community-based organizations, civil society groups, networks of key populations (KP), networks and associations of people living with HIV (PLHIV), women-led civil society 1 organizations, youth-led civil society organizations, and other affected groups or community entities that work on health, HIV program, gather quantitative and qualitative data on HIV services and advocate for necessary policy and program changes. These organizations should have a clear mission and activities focused on HIV programming.

The NIGMS Postdoctoral Research Associate Training (PRAT) Programs overarching goal is to provide high quality postdoctoral research training in the basic biomedical sciences to a diverse group of postdoctoral fellows in NIH intramural research laboratories, and to prepare them for leadership positions in careers in the biomedical research workforce. Research projects proposed should fall within basic biomedical fields relevant to the NIGMS mission. In addition to the laboratory experience, the PRAT program provides a structured training environment with extensive career and professional development, mentoring, and networking opportunities planned and supported by the program.

The purpose of this project is to provide implementation support and technical assistance to the districts, health facilities, community-based providers, and communities, in planning, delivery, and monitoring of facility and community-based malaria services, including malaria case management, prevention of malaria in pregnancy, and social and behavior change (SBC).

To support outstanding graduate students from diverse backgrounds, including those from groups underrepresented in biomedical, clinical, behavioral and social sciences, over the transition from predoctoral to postdoctoral research training.. This phased award program will facilitate completion of graduate PhD or dual degree clinician scientist programs (F99) and progression to mentored postdoctoral positions in dental, oral and craniofacial research (K00).

The Rural Economic Development Loan and Grant program provides funding for rural projects through local utility organizations. USDA provides zero-interest loans to local utilities which they, in turn, pass through to local businesses (ultimate recipients) for projects that will create and retain employment in rural areas. The ultimate recipients repay the lending utility directly. The utility then is responsible for repayment to USDA. USDA provides grants to local utility organizations which use the funding to establish Revolving Loan Funds (RLF). Loans are made from the revolving loan funds to projects that will create or retain rural jobs. When the revolving loan fund is terminated, the grant is repaid to USDA.The Agency anticipates the following maximum amounts per award: Loans - $2,000,000; Grants - $300,000.

Designed to assist individuals with severe disabilities and their families to remain together in their homes and communities. Services are designed to be flexible and responsive to individual or family needs. Services can include but are not limited to: Respite care, day care services, home modifications, equipment, supplies, personal assistance, transportation, homemaker services, housing costs, health related needs, nursing and counseling.

This funding opportunity supports research training for students from underrepresented backgrounds in health disparities and minority health, enabling them to gain valuable experience through domestic and international research programs.

This funding opportunity provides financial support to public health departments already receiving CDC funding to enhance their environmental health capabilities through data-driven projects addressing COVID-19 mitigation and pediatric cancer monitoring.

This program provides financial assistance to small rural hospitals with 49 or fewer beds to help them improve healthcare quality and meet Medicare data system requirements, including implementing new coding systems and enhancing patient care reporting.

Amendment 1 to Notice of Funding Opportunity (NOFO) No. 72062024RFA00003The purpose of Amendment Number 01 to NOFO No. 72062024RFA00003 is to:1. Provide formal responses to the question received by the due date indicated in the NOFO;2. Extend the closing date for the submission of the concept slides from June 12, 2024, to June 14, 2024, and;3. Provide a gender analysis as referenced in the program description.Please note that the attached responses to the questions are hereby incorporated as part of NOFO Number 72062024RFA00003.All other terms and conditions of the NOFO, as amended, remain unchanged and in full force and effect.

The Sexual Assault Services Program provides intervention, advocacy, accompaniment (i.e., accompanying victims to court, medical facilities, police departments, etc.), support services, and related assistance for adult, youth, and child victims of sexual assault, family and household members of victims, and those collaterally affected by the sexual assault. SASP, created by the Violence Against Women and Department of Justice Reauthorization Act of 2005, 42 U.S.C. §14043g, is the first federal funding stream solely dedicated to the provision of direct intervention and related assistance for victims of sexual assault. SASP provides intervention, advocacy, accompaniment (i.e., accompanying victims to court, medical facilities, police departments, etc.), support services, and related assistance for adult, youth, and child victims of sexual assault, family and household members of victims, and those collaterally affected by the sexual assault. Rape crisis centers play a vital role in assisting sexual assault victims through the healing process, as well as assisting victims through the medical, criminal justice, and other social support systems. In order to provide comprehensive services to victims of sexual assault, SASP assists states in supporting rape crisis centers in the provision of direct intervention and related assistance.

Utilizing CMP funds from the federal CMS, an organization, agency, or entity would provide training to long-term care facility staff regarding ensuring proper resident hygiene, nutrition, and promoting social interation. In an effort to support the maintenance of cognitive and mobility skills, the Illinois Department of Public Health, Office of Healthcare Regulation (OHCR) announces an opportunity for certified facilities to submit applications to implementation changes to increase the quality of life within their facility. This grant seeks to provide facility staff training in the areas of; (1) showering and personal care, (2) nutrition, choking, and dietary issues, (3) social interaction / social isolation, and (4) showering and personal care. By addressing each topic individually for two hours bi-annually, the overall quality of life within Long Term Care facilities will increase.