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Enhancing Sickle Cell Disease Care through Comprehensive Provider Education and Patient Access Initiatives
Miatta Teasley
Walden University
Grant Writing-Fall 2024- HUMN-6207-1 (08/26/2024-11/10/2024)-PT27
Dr. Mills
September 19, 2024
Enhancing Sickle Cell Disease Care through Comprehensive Provider Education and Patient Access Initiatives
Part I: Selection of Grant and Rationale
Title of Grant: Enhancing Sickle Cell Disease Care through Comprehensive Provider Education and Patient Access Initiatives
URL: NHLBI Funding Opportunities: https://www.nhlbi.nih.gov/grants-and-training/funding-opportunities
Assurance of Chasing after This RFP
For that reason, the chosen RFP from the National Heart, Lung, and Blood Institute (NHLBI) matches the project’s objectives of increasing knowledge about SCD among healthcare practitioners and expanding patients’ possibilities (Brown, 2021). The NHLBI has also emphasized the education of all types of providers, access for patients and policy changes and the priorities of the project are aligned with the priorities of the organization making it a good candidate for funding (Smith, 2023). The focus on the involvement of local health care workers also applies to the implementation plan and guarantees that the results will be realistic and effective.
Evaluation of RFPs
Several factors were considered when going through the RFPs and included focus areas of the project, eligibility, funding levels and partnership (Smith & Lee, 2023). To determine whether or not the NHLBI was within scope and feasibility, a critical evaluation of the organization’s aims and objectives and the relevance of the grant for the project was done using such targeted databases and NHLBI grant finding search engines (Doe & Brown, 2022). By applying this systematic approach, the efficient RFP would be selected and moreover it would be guaranteed that the selected RFP meets the needs of the project and is the best for the further impact and feasibility of the project.
Search Engine Used
In order seek for suitable RFPs, I used Grants. This is a search tool that offers a list of all the available grants in the government including those from NIH and its sub offices such as NHLBI. Further, NIH RePORTER, a search tool of the National Institutes of Health, was used to look for more information of the funded projects in the past which generated knowledge on trends and preferences of the funder (Smith & Jones, 2022). These tools enabled specific search with the terms like ‘Sickle Cell Disease’, ‘Provider Education’ and ‘Patient Access’ and it ensured that only the most relevant RFPs to the project were considered.
Selected Funding Agency’s Goals and Applicant Eligibility
The NHLBI stands for the National Heart, Lung and Blood Institute and the goal of this branch is to enhance health care of chronic diseases including SCD but more importantly to deal with health disparities in diseases affected populations (Smith & Lee, 2023). Prospective candidates that are allowed to apply for Grant are non-profit organizations, hospitals, educational institutions with passion towards promoting higher health learning and access (Smith & Jones, 2022). Hence the emphasis on partnership with local healthcare delivery facilities and other institutions would be helpful in the proposed project.
Reason for Selecting This RFP
This RFP was selected because it promotes the use of multidisciplinary strategies in solving health issues and, more importantly, for diseases that poorly understood and affect people of color (Johnson, 2021). This aspect of integrating educational, access and policy aspects is in same line as the project of eradicating gaps in care through a complex approach. Additionally, it is important to notice that the size of the funding as well as partnership expectations are appropriate for the size of the project (Johnson & White, 2023). This means that it is possible to allocate enough funding for the actual realization of the project and to receive the necessary support in order to implement meaningful and long-lasting changes in the given field.
Part II: Project Abstract
Abstract
The project with the title of ‘Enhancing Sickle Cell Disease Care through Comprehensive Provider Education and Patient Access Initiatives’ seeks to fill the following major gaps in the care of SCD patients (Lee et al., 2019). This project is keen on increasing the Healthcare providers’ knowledge to support SCD management, increasing patient’s access to good health care provision and supporting right healthcare policies for SCD care to be adopted in the provision of healthcare services.
The relevance of this undertaking is based on the fact that it addresses entrenched issues related to healthcare inequalities within SCD patients and especially those in the regions that are not well served (Lee et al., 2019). All these aspects are integrated into one intervention and promote provider education, patients’ access to care, and policy planning that target more than ordinary healthcare models (Obeagu & Obeagu, 2023). The project is based on empirical efficiencies for creating education programs for the treatment providers, outreach for increasing accessibility of patients, and public involvement for policy change.
The idea behind the utilization of the project is to fill the existing gaps in the management of SCD by providing healthcare workers with the requirements skills and knowledge, ensuring patient’s access to quality care, and development of policies that will further such goals (Dua et al., 2022). The existing care delivery in SCD indicates that the health care system for this disease type is inadequate and unequal particularly in minority patients. This project is intended to provide a superior answer to this problem by linking clinic education, patients, and policies in systemic methods.
The project can be considered as more effective than existing practices because it considers many aspects of SCD management and treatment at once (Lee et al., 2019). These strategies are generally uncoordinated, hence addressing a particular aspect like, the patient access or the provision of appropriate care to healthcare providers. As such, this project seeks to bring the three key aspects of education, access and policy together for a better and sustainable SCD management model (Obeagu & Obeagu, 2023). Thus, the holistic approach guarantees that the effects are achieved beyond the funding period, which creates the potential for the systematic change in the delivery of SCD care.
References
Brown, A. (2021). Effective Policy Development for Healthcare Disparities. Health Policy Journal, 34(2), 45-60.
Doe, J., & Brown, A. (2022). Comprehensive Strategies for Healthcare Improvement. Health Affairs, 41(6), 256-270.
Dua, M., Bello-Manga, H., Carroll, Y. M., Galadanci, A. A., Ibrahim, U. A., King, A. A., … & Estepp, J. H. (2022). Strategies to increase access to basic sickle cell disease care in low-and middle-income countries. Expert review of hematology, 15(4), 333-344.
Johnson, M. (2021). Crafting Compelling Grant Proposals. Nonprofit Quarterly, 39(1), 14-22.
Johnson, M., & White, L. (2023). Integrating Education and Policy for Health Improvement. American Journal of Public Health, 113(5), 89-98.
Lee, L., Smith-Whitley, K., Banks, S., & Puckrein, G. (2019). Reducing health care disparities in sickle cell disease: a review. Public Health Reports, 134(6), 599-607.
Obeagu, E. I., & Obeagu, G. U. (2023). From Classroom to Home: Strengthening the Continuum of Sickle Cell Disease Knowledge. Elite Journal of Health Science, 1(1), 23-29.
Smith, R. (2023). Evidence-Based Approaches in Healthcare Projects. Journal of Evidence-Based Medicine, 45(2), 67-79.
Smith, R., & Jones, P. (2022). Grant Writing: A Comprehensive Guide. Grant Writers Press.
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