Lupus is a severe autoimmune disease, often misdiagnosed and disproportionately affecting women and specific ethnic groups, leading to significant health disparities and negative outcomes. This Public Health Department grant aims to reduce time to diagnosis, improve care access, enhance care coordination, and improve quality of life for individuals with lupus. It supports national organizations to implement two key strategies. The first focuses on increasing healthcare provider awareness, knowledge, and skills through training, technology integration, and care transition guidance. The second promotes the national uptake and use of effective lupus self-management tools and services among targeted populations and stakeholders, utilizing existing campaigns and electronic health records. This initiative seeks to improve self-management behaviors and overall health outcomes for people living with lupus.
Opportunity ID: 325995
General Information
| Document Type: | Grants Notice |
| Funding Opportunity Number: | CDC-RFA-DP20-2008 |
| Funding Opportunity Title: | Developing and Disseminating Strategies to Build Sustainable Lupus Awareness, Knowledge, Skills, and Partnerships |
| Opportunity Category: | Discretionary |
| Opportunity Category Explanation: | – |
| Funding Instrument Type: | Cooperative Agreement |
| Category of Funding Activity: | Health |
| Category Explanation: | – |
| Expected Number of Awards: | 2 |
| Assistance Listings: | 93.068 — Chronic Diseases: Research, Control, and Prevention |
| Cost Sharing or Matching Requirement: | No |
| Version: | Synopsis 2 |
| Posted Date: | May 01, 2020 |
| Last Updated Date: | May 04, 2020 |
| Original Closing Date for Applications: | Jun 26, 2020 Electronically submitted applications must be submitted no later than 11:59 p.m., ET, on the listed application due date. |
| Current Closing Date for Applications: | Jun 26, 2020 Electronically submitted applications must be submitted no later than 11:59 p.m., ET, on the listed application due date. |
| Archive Date: | Jul 26, 2020 |
| Estimated Total Program Funding: | $2,670,230 |
| Award Ceiling: | $1,500,000 |
| Award Floor: | $1,100,000 |
Eligibility
| Eligible Applicants: | State governments For profit organizations other than small businesses Nonprofits that do not have a 501(c)(3) status with the IRS, other than institutions of higher education Nonprofits having a 501(c)(3) status with the IRS, other than institutions of higher education Public and State controlled institutions of higher education Private institutions of higher education Special district governments Unrestricted (i.e., open to any type of entity above), subject to any clarification in text field entitled “Additional Information on Eligibility” |
| Additional Information on Eligibility: | CDC will not accept and review applications with budgets greater than the ceiling of the award range ($1.5 Million). Applications with budgets that exceed the ceiling of the award will be considered non-responsive and will not be entered into the review process. |
Additional Information
| Agency Name: | Centers for Disease Control – NCCDPHP |
| Description: | Lupus is a systemic autoimmune disease. It is estimated 161,000 to 322,000 Americans have the most common type of lupus, systemic lupus erythematosus (SLE). Although anyone can get lupus, 9 out of 10 diagnoses of lupus are in women ages 15 to 44. African American and Latino women are at greater risk for lupus than white women and usually get it at a younger age and have more severe symptoms. Lupus is also more common in Hispanic, Asian, and Native American and Alaskan Native women. The causes of lupus are unknown but are believed to be linked to genetic, environmental, and hormonal factors.Lupus is difficult to diagnose, hard to live with and challenging to treat. Lupus has a range of symptoms often confused with other conditions, making it difficult to recognize and diagnose. Its symptoms and outcomes can be severe or fatal, its onset can be sudden, its causes are unclear and there is no known cure.This NOFO addresses several persisting gaps and inequities related to lupus. Lupus can result in a range of negative outcomes including disability, social stigma, lost productivity, absence from the workforce, reduction in quality of life, organ damage or failure or early death. Undiagnosed or late diagnosis of lupus can increase the likelihood or worsen the severity of many of these outcomes. Even with a correct diagnosis, lupus is challenging to treat. Much is needed to improve the care and quality of life for people living with the disease. The public health sector can contribute a great deal to this end and help mitigate these gaps and inequities.The purpose of the NOFO is to support national organizations implementing national efforts to help reduce time to lupus diagnoses, increase number of people with lupus getting needed care and ongoing treatment, improve lupus care, care transition and care coordination, improve lupus patients’ self-management behaviors, and improve quality of life and health outcomes among people with lupus. This NOFO will focus on two key strategies and their associated activities:Strategy A: Increase awareness, knowledge and skills among healthcare providers to appropriately recognize the signs and symptoms of lupus, what to do if lupus is suspected, and provide quality, well-coordinated lupus care. Activities are to:Develop and promote healthcare provider lupus training and education.Increase the role of technology in the clinical setting.Collaborate with health professional associations to establish or increase sustainable educational opportunities.Develop and promote practice procedures for transition of lupus care from pediatric to adult care.Strategy B: In collaboration with key stakeholders promote the national uptake and use of effective lupus self-management tools and/or services. Activities are to:Raise awareness about lupus signs and symptoms and what to do if you have lupus among targeted populations using existing national lupus campaigns, websites, and tools.Support implementation and evaluation of lupus-specific self-management tools and/or services.Promote the national uptake and use of lupus self-management tools and/or services among women ages 15 to 44 and key stakeholders.Apply electronic health or medical record systems or other medical information technology to refer patients to appropriate lupus self-management tools/services, and track patient information.Identify and address lupus patients’ barriers to access effective lupus self-management tools and/or services.These strategies and activities are intended to result in the following outcomes:Increased number of healthcare providers recognizing the signs and symptoms of lupus and what to do if lupus is suspected.Increased number of healthcare providers using tele-health and/or electronic health records to identify lupus cases and treatment gaps.Increased number of settings receiving guidance on transition of pediatric lupus care to adult care.Increased number of people living with lupus engaged in the use of lupus self-management tools and/or services.Increased number of referrals to lupus self-management tools and/or services using electronic health or medical record systems or other medical information technology.Improved self-management behaviors among people with lupus.The NOFO will fund TWO awards, ONE award will be issued for each Strategy. Applicant can apply for one or both Strategies but must submit a separate application for each Strategy. A total of $2,670,230 is available for annual funding, a range of $1.1 Million to $1.5 Million will be awarded to each successful applicant. |
| Link to Additional Information: | https://www.cdc.gov/lupus/funded/nofo/cdc-rfa-dp20-2008.html |
| Grantor Contact Information: | If you have difficulty accessing the full announcement electronically, please contact:
Margaret Kaniewski
mgk6@cdc.gov Email:mgk6@cdc.gov |
Version History
| Version | Modification Description | Updated Date |
|---|---|---|
| Eligibility Categories were updated. | May 04, 2020 | |
| May 01, 2020 | ||
| The word "expected" was changed to "suspected" for expected outcome measures. | Apr 02, 2020 | |
| The word "expected" was changed to "suspected" for expected outcome measures. | Apr 02, 2020 | |
| Made changes to the activities listed above. | Apr 02, 2020 | |
| Made changes to the activities listed above. | Apr 02, 2020 | |
| Apr 02, 2020 |
DISPLAYING: Synopsis 2
General Information
| Document Type: | Grants Notice |
| Funding Opportunity Number: | CDC-RFA-DP20-2008 |
| Funding Opportunity Title: | Developing and Disseminating Strategies to Build Sustainable Lupus Awareness, Knowledge, Skills, and Partnerships |
| Opportunity Category: | Discretionary |
| Opportunity Category Explanation: | – |
| Funding Instrument Type: | Cooperative Agreement |
| Category of Funding Activity: | Health |
| Category Explanation: | – |
| Expected Number of Awards: | 2 |
| Assistance Listings: | 93.068 — Chronic Diseases: Research, Control, and Prevention |
| Cost Sharing or Matching Requirement: | No |
| Version: | Synopsis 2 |
| Posted Date: | May 01, 2020 |
| Last Updated Date: | May 04, 2020 |
| Original Closing Date for Applications: | Jun 26, 2020 Electronically submitted applications must be submitted no later than 11:59 p.m., ET, on the listed application due date. |
| Current Closing Date for Applications: | Jun 26, 2020 Electronically submitted applications must be submitted no later than 11:59 p.m., ET, on the listed application due date. |
| Archive Date: | Jul 26, 2020 |
| Estimated Total Program Funding: | $2,670,230 |
| Award Ceiling: | $1,500,000 |
| Award Floor: | $1,100,000 |
Eligibility
| Eligible Applicants: | State governments For profit organizations other than small businesses Nonprofits that do not have a 501(c)(3) status with the IRS, other than institutions of higher education Nonprofits having a 501(c)(3) status with the IRS, other than institutions of higher education Public and State controlled institutions of higher education Private institutions of higher education Special district governments Unrestricted (i.e., open to any type of entity above), subject to any clarification in text field entitled “Additional Information on Eligibility” |
| Additional Information on Eligibility: | CDC will not accept and review applications with budgets greater than the ceiling of the award range ($1.5 Million). Applications with budgets that exceed the ceiling of the award will be considered non-responsive and will not be entered into the review process. |
Additional Information
| Agency Name: | Centers for Disease Control – NCCDPHP |
| Description: | Lupus is a systemic autoimmune disease. It is estimated 161,000 to 322,000 Americans have the most common type of lupus, systemic lupus erythematosus (SLE). Although anyone can get lupus, 9 out of 10 diagnoses of lupus are in women ages 15 to 44. African American and Latino women are at greater risk for lupus than white women and usually get it at a younger age and have more severe symptoms. Lupus is also more common in Hispanic, Asian, and Native American and Alaskan Native women. The causes of lupus are unknown but are believed to be linked to genetic, environmental, and hormonal factors.Lupus is difficult to diagnose, hard to live with and challenging to treat. Lupus has a range of symptoms often confused with other conditions, making it difficult to recognize and diagnose. Its symptoms and outcomes can be severe or fatal, its onset can be sudden, its causes are unclear and there is no known cure.This NOFO addresses several persisting gaps and inequities related to lupus. Lupus can result in a range of negative outcomes including disability, social stigma, lost productivity, absence from the workforce, reduction in quality of life, organ damage or failure or early death. Undiagnosed or late diagnosis of lupus can increase the likelihood or worsen the severity of many of these outcomes. Even with a correct diagnosis, lupus is challenging to treat. Much is needed to improve the care and quality of life for people living with the disease. The public health sector can contribute a great deal to this end and help mitigate these gaps and inequities.The purpose of the NOFO is to support national organizations implementing national efforts to help reduce time to lupus diagnoses, increase number of people with lupus getting needed care and ongoing treatment, improve lupus care, care transition and care coordination, improve lupus patients’ self-management behaviors, and improve quality of life and health outcomes among people with lupus. This NOFO will focus on two key strategies and their associated activities:Strategy A: Increase awareness, knowledge and skills among healthcare providers to appropriately recognize the signs and symptoms of lupus, what to do if lupus is suspected, and provide quality, well-coordinated lupus care. Activities are to:Develop and promote healthcare provider lupus training and education.Increase the role of technology in the clinical setting.Collaborate with health professional associations to establish or increase sustainable educational opportunities.Develop and promote practice procedures for transition of lupus care from pediatric to adult care.Strategy B: In collaboration with key stakeholders promote the national uptake and use of effective lupus self-management tools and/or services. Activities are to:Raise awareness about lupus signs and symptoms and what to do if you have lupus among targeted populations using existing national lupus campaigns, websites, and tools.Support implementation and evaluation of lupus-specific self-management tools and/or services.Promote the national uptake and use of lupus self-management tools and/or services among women ages 15 to 44 and key stakeholders.Apply electronic health or medical record systems or other medical information technology to refer patients to appropriate lupus self-management tools/services, and track patient information.Identify and address lupus patients’ barriers to access effective lupus self-management tools and/or services.These strategies and activities are intended to result in the following outcomes:Increased number of healthcare providers recognizing the signs and symptoms of lupus and what to do if lupus is suspected.Increased number of healthcare providers using tele-health and/or electronic health records to identify lupus cases and treatment gaps.Increased number of settings receiving guidance on transition of pediatric lupus care to adult care.Increased number of people living with lupus engaged in the use of lupus self-management tools and/or services.Increased number of referrals to lupus self-management tools and/or services using electronic health or medical record systems or other medical information technology.Improved self-management behaviors among people with lupus.The NOFO will fund TWO awards, ONE award will be issued for each Strategy. Applicant can apply for one or both Strategies but must submit a separate application for each Strategy. A total of $2,670,230 is available for annual funding, a range of $1.1 Million to $1.5 Million will be awarded to each successful applicant. |
| Link to Additional Information: | https://www.cdc.gov/lupus/funded/nofo/cdc-rfa-dp20-2008.html |
| Grantor Contact Information: | If you have difficulty accessing the full announcement electronically, please contact:
Margaret Kaniewski
mgk6@cdc.gov Email:mgk6@cdc.gov |
DISPLAYING: Synopsis 1
General Information
| Document Type: | Grants Notice |
| Funding Opportunity Number: | CDC-RFA-DP20-2008 |
| Funding Opportunity Title: | Developing and Disseminating Strategies to Build Sustainable Lupus Awareness, Knowledge, Skills, and Partnerships |
| Opportunity Category: | Discretionary |
| Opportunity Category Explanation: | – |
| Funding Instrument Type: | Cooperative Agreement |
| Category of Funding Activity: | Health |
| Category Explanation: | – |
| Expected Number of Awards: | 2 |
| Assistance Listings: | 93.068 — Chronic Diseases: Research, Control, and Prevention |
| Cost Sharing or Matching Requirement: | No |
| Version: | Synopsis 1 |
| Posted Date: | May 01, 2020 |
| Last Updated Date: | May 01, 2020 |
| Original Closing Date for Applications: | – |
| Current Closing Date for Applications: | Jun 26, 2020 Electronically submitted applications must be submitted no later than 11:59 p.m., ET, on the listed application due date. |
| Archive Date: | Jul 26, 2020 |
| Estimated Total Program Funding: | $2,670,230 |
| Award Ceiling: | $1,500,000 |
| Award Floor: | $1,100,000 |
Eligibility
| Eligible Applicants: | Nonprofits having a 501(c)(3) status with the IRS, other than institutions of higher education Private institutions of higher education For profit organizations other than small businesses Unrestricted (i.e., open to any type of entity above), subject to any clarification in text field entitled “Additional Information on Eligibility” Nonprofits that do not have a 501(c)(3) status with the IRS, other than institutions of higher education State governments Special district governments Public and State controlled institutions of higher education |
| Additional Information on Eligibility: | CDC will not accept and review applications with budgets greater than the ceiling of the award range ($1.5 Million). Applications with budgets that exceed the ceiling of the award will be considered non-responsive and will not be entered into the review process. |
Additional Information
| Agency Name: | Centers for Disease Control – NCCDPHP |
| Description: | Lupus is a systemic autoimmune disease. It is estimated 161,000 to 322,000 Americans have the most common type of lupus, systemic lupus erythematosus (SLE). Although anyone can get lupus, 9 out of 10 diagnoses of lupus are in women ages 15 to 44. African American and Latino women are at greater risk for lupus than white women and usually get it at a younger age and have more severe symptoms. Lupus is also more common in Hispanic, Asian, and Native American and Alaskan Native women. The causes of lupus are unknown but are believed to be linked to genetic, environmental, and hormonal factors. Lupus is difficult to diagnose, hard to live with and challenging to treat. Lupus has a range of symptoms often confused with other conditions, making it difficult to recognize and diagnose. Its symptoms and outcomes can be severe or fatal, its onset can be sudden, its causes are unclear and there is no known cure. This NOFO addresses several persisting gaps and inequities related to lupus. Lupus can result in a range of negative outcomes including disability, social stigma, lost productivity, absence from the workforce, reduction in quality of life, organ damage or failure or early death. Undiagnosed or late diagnosis of lupus can increase the likelihood or worsen the severity of many of these outcomes. Even with a correct diagnosis, lupus is challenging to treat. Much is needed to improve the care and quality of life for people living with the disease. The public health sector can contribute a great deal to this end and help mitigate these gaps and inequities. The purpose of the NOFO is to support national organizations implementing national efforts to help reduce time to lupus diagnoses, increase number of people with lupus getting needed care and ongoing treatment, improve lupus care, care transition and care coordination, improve lupus patients’ self-management behaviors, and improve quality of life and health outcomes among people with lupus. This NOFO will focus on two key strategies and their associated activities: Strategy A: Increase awareness, knowledge and skills among healthcare providers to appropriately recognize the signs and symptoms of lupus, what to do if lupus is suspected, and provide quality, well-coordinated lupus care. Activities are to: Develop and promote healthcare provider lupus training and education. Strategy B: In collaboration with key stakeholders promote the national uptake and use of effective lupus self-management tools and/or services. Activities are to: Raise awareness about lupus signs and symptoms and what to do if you have lupus among targeted populations using existing national lupus campaigns, websites, and tools. These strategies and activities are intended to result in the following outcomes: Increased number of healthcare providers recognizing the signs and symptoms of lupus and what to do if lupus is suspected. The NOFO will fund TWO awards, ONE award will be issued for each Strategy. Applicant can apply for one or both Strategies but must submit a separate application for each Strategy. A total of $2,670,230 is available for annual funding, a range of $1.1 Million to $1.5 Million will be awarded to each successful applicant. |
| Link to Additional Information: | https://www.cdc.gov/lupus/funded/nofo/cdc-rfa-dp20-2008.html |
| Grantor Contact Information: | If you have difficulty accessing the full announcement electronically, please contact:
Margaret Kaniewski
mgk6@cdc.gov Email:mgk6@cdc.gov |
DISPLAYING: Forecast 5
General Information
| Document Type: | Grants Notice |
| Funding Opportunity Number: | CDC-RFA-DP20-2008 |
| Funding Opportunity Title: | Developing and Disseminating Strategies to Build Sustainable Lupus Awareness, Knowledge, Skills, and Partnerships |
| Opportunity Category: | Discretionary |
| Opportunity Category Explanation: | – |
| Funding Instrument Type: | Cooperative Agreement |
| Category of Funding Activity: | Health |
| Category Explanation: | – |
| Expected Number of Awards: | 2 |
| Assistance Listings: | 93.068 — Chronic Diseases: Research, Control, and Prevention |
| Cost Sharing or Matching Requirement: | No |
| Version: | Forecast 5 |
| Posted Date: | Apr 02, 2020 |
| Last Updated Date: | Apr 07, 2020 |
| Original Closing Date for Applications: | – |
| Current Closing Date for Applications: | – |
| Archive Date: | Jul 26, 2020 |
| Estimated Total Program Funding: | $2,670,230 |
| Award Ceiling: | $1,500,000 |
| Award Floor: | $1,100,000 |
Eligibility
| Eligible Applicants: | Unrestricted (i.e., open to any type of entity above), subject to any clarification in text field entitled “Additional Information on Eligibility” |
| Additional Information on Eligibility: |
Additional Information
| Agency Name: | Centers for Disease Control – NCCDPHP |
| Description: | Lupus is a systemic autoimmune disease. It is estimated 161,000 to 322,000 Americans have the most common type of lupus, systemic lupus erythematosus (SLE). Although anyone can get lupus, 9 out of 10 diagnoses of lupus are in women ages 15 to 44. African American and Latino women are at greater risk for lupus than white women and usually get it at a younger age and have more severe symptoms. Lupus is also more common in Hispanic, Asian, and Native American and Alaskan Native women. The causes of lupus are unknown but are believed to be linked to genetic, environmental, and hormonal factors. Lupus is difficult to diagnose, hard to live with and challenging to treat. Lupus has a range of symptoms often confused with other conditions, making it difficult to recognize and diagnose. Its symptoms and outcomes can be severe or fatal, its onset can be sudden, its causes are unclear and there is no known cure. This NOFO addresses several persisting gaps and inequities related to lupus. Lupus can result in a range of negative outcomes including disability, social stigma, lost productivity, absence from the workforce, reduction in quality of life, organ damage or failure or early death. Undiagnosed or late diagnosis of lupus can increase the likelihood or worsen the severity of many of these outcomes. Even with a correct diagnosis, lupus is challenging to treat. Much is needed to improve the care and quality of life for people living with the disease. The public health sector can contribute a great deal to this end and help mitigate these gaps and inequities. The purpose of the NOFO is to support national organizations implementing national efforts to help reduce time to lupus diagnoses, increase number of people with lupus getting needed care and ongoing treatment, improve lupus care, care transition and care coordination, improve lupus patients’ self-management behaviors, and improve quality of life and health outcomes among people with lupus. This NOFO will focus on two key strategies and their associated activities: Strategy: Increase awareness, knowledge and skills among healthcare providers to appropriately recognize the signs and symptoms of lupus, what to do if lupus is suspected, and provide quality, well-coordinated lupus care. Activities are to: Develop and promote healthcare provider lupus training and education. Strategy: In collaboration with key stakeholders promote the national uptake and use of effective lupus self-management tools and/or services. Activities are to: Support implementation and evaluation of lupus-specific self-management tools and/or services. These strategies and activities are intended to result in the following outcome measures: Increased number of healthcare providers recognizing the signs and symptoms of lupus and what to do if lupus is suspected. The NOFO will fund TWO awards, ONE award will be issued for each Strategy. Applicant can apply for one or both Strategies but must submit a separate application for each Strategy. A total of $2,670,230 is available for annual funding, a range of $1.1 Million to $1.5 Million will be awarded to each successful applicant. |
| Link to Additional Information: | – |
| Grantor Contact Information: | If you have difficulty accessing the full announcement electronically, please contact:
–
Email:mgk6@cdc.gov |
DISPLAYING: Forecast 4
General Information
| Document Type: | Grants Notice |
| Funding Opportunity Number: | CDC-RFA-DP20-2008 |
| Funding Opportunity Title: | Developing and Disseminating Strategies to Build Sustainable Lupus Awareness, Knowledge, Skills, and Partnerships |
| Opportunity Category: | Discretionary |
| Opportunity Category Explanation: | – |
| Funding Instrument Type: | Cooperative Agreement |
| Category of Funding Activity: | Health |
| Category Explanation: | – |
| Expected Number of Awards: | 2 |
| Assistance Listings: | 93.068 — Chronic Diseases: Research, Control, and Prevention |
| Cost Sharing or Matching Requirement: | No |
| Version: | Forecast 4 |
| Posted Date: | Apr 02, 2020 |
| Last Updated Date: | Apr 07, 2020 |
| Original Closing Date for Applications: | – |
| Current Closing Date for Applications: | – |
| Archive Date: | Jul 26, 2020 |
| Estimated Total Program Funding: | $2,670,230 |
| Award Ceiling: | $1,500,000 |
| Award Floor: | $1,100,000 |
Eligibility
| Eligible Applicants: | Unrestricted (i.e., open to any type of entity above), subject to any clarification in text field entitled “Additional Information on Eligibility” |
| Additional Information on Eligibility: |
Additional Information
| Agency Name: | Centers for Disease Control – NCCDPHP |
| Description: | Lupus is a systemic autoimmune disease. It is estimated 161,000 to 322,000 Americans have the most common type of lupus, systemic lupus erythematosus (SLE). Although anyone can get lupus, 9 out of 10 diagnoses of lupus are in women ages 15 to 44. African American and Latino women are at greater risk for lupus than white women and usually get it at a younger age and have more severe symptoms. Lupus is also more common in Hispanic, Asian, and Native American and Alaskan Native women. The causes of lupus are unknown but are believed to be linked to genetic, environmental, and hormonal factors.Lupus is difficult to diagnose, hard to live with and challenging to treat. Lupus has a range of symptoms often confused with other conditions, making it difficult to recognize and diagnose. Its symptoms and outcomes can be severe or fatal, its onset can be sudden, its causes are unclear and there is no known cure.This NOFO addresses several persisting gaps and inequities related to lupus. Lupus can result in a range of negative outcomes including disability, social stigma, lost productivity, absence from the workforce, reduction in quality of life, organ damage or failure or early death. Undiagnosed or late diagnosis of lupus can increase the likelihood or worsen the severity of many of these outcomes. Even with a correct diagnosis, lupus is challenging to treat. Much is needed to improve the care and quality of life for people living with the disease. The public health sector can contribute a great deal to this end and help mitigate these gaps and inequities.The purpose of the NOFO is to support national organizations implementing national efforts to help reduce time to lupus diagnoses, increase number of people with lupus getting needed care and ongoing treatment, improve lupus care, care transition and care coordination, improve lupus patients’ self-management behaviors, and improve quality of life and health outcomes among people with lupus. This NOFO will focus on two key strategies and their associated activities:Strategy: Increase awareness, knowledge and skills among healthcare providers to appropriately recognize the signs and symptoms of lupus, what to do if lupus is expected, and provide quality, well-coordinated lupus care. Activities are to:Develop and promote healthcare provider lupus training and education.Increase the role of technology in the clinical setting.Collaborate with health professional associations to establish or increase sustainable educational opportunities.Develop and promote practice procedures for transition of lupus care from pediatric to adult care.Strategy: In collaboration with key stakeholders promote the national uptake and use of effective lupus self-management tools and/or services. Activities are to:Support implementation and evaluation of lupus-specific self-management tools and/or services.Promote the national uptake and use of lupus self-management tools and/or services among women ages 15 to 44 and key stakeholders.Apply electronic health or medical record systems or other medical information technology to refer patients to appropriate lupus self-management tools/services, and track patient information.Identify and address lupus patients’ barriers to access effective lupus self-management tools and/or services.These strategies and activities are intended to result in the following outcome measures:Increased number of healthcare providers recognizing the signs and symptoms of lupus and what to do if lupus is expected.Increased number of healthcare providers using tele-health and/or electronic health records to identify lupus cases and treatment gaps.Increased number of settings receiving guidance on transition of pediatric lupus care to adult care.Increased number of people living with lupus engaged in the use of lupus self-management tools and/or services.Increased number of referrals to lupus self-management tools and/or services using electronic health or medical record systems or other medical information technology.Improved self-management behaviors among people with lupus.The NOFO will fund TWO awards, ONE award will be issued for each Strategy. Applicant can apply for one or both Strategies but must submit a separate application for each Strategy. A total of $2,670,230 is available for annual funding, a range of $1.1 Million to $1.5 Million will be awarded to each successful applicant. |
| Link to Additional Information: | – |
| Grantor Contact Information: | If you have difficulty accessing the full announcement electronically, please contact:
–
Email:mgk6@cdc.gov |
DISPLAYING: Forecast 3
General Information
| Document Type: | Grants Notice |
| Funding Opportunity Number: | CDC-RFA-DP20-2008 |
| Funding Opportunity Title: | Developing and Disseminating Strategies to Build Sustainable Lupus Awareness, Knowledge, Skills, and Partnerships |
| Opportunity Category: | Discretionary |
| Opportunity Category Explanation: | – |
| Funding Instrument Type: | Cooperative Agreement |
| Category of Funding Activity: | Health |
| Category Explanation: | – |
| Expected Number of Awards: | 2 |
| Assistance Listings: | 93.068 — Chronic Diseases: Research, Control, and Prevention |
| Cost Sharing or Matching Requirement: | No |
| Version: | Forecast 3 |
| Posted Date: | Apr 02, 2020 |
| Last Updated Date: | Apr 02, 2020 |
| Original Closing Date for Applications: | – |
| Current Closing Date for Applications: | – |
| Archive Date: | Jul 26, 2020 |
| Estimated Total Program Funding: | $2,670,230 |
| Award Ceiling: | $1,500,000 |
| Award Floor: | $1,100,000 |
Eligibility
| Eligible Applicants: | Unrestricted (i.e., open to any type of entity above), subject to any clarification in text field entitled “Additional Information on Eligibility” |
| Additional Information on Eligibility: |
Additional Information
| Agency Name: | Centers for Disease Control – NCCDPHP |
| Description: | Lupus is a systemic autoimmune disease. It is estimated 161,000 to 322,000 Americans have the most common type of lupus, systemic lupus erythematosus (SLE). Although anyone can get lupus, 9 out of 10 diagnoses of lupus are in women ages 15 to 44. African American and Latino women are at greater risk for lupus than white women and usually get it at a younger age and have more severe symptoms. Lupus is also more common in Hispanic, Asian, and Native American and Alaskan Native women. The causes of lupus are unknown but are believed to be linked to genetic, environmental, and hormonal factors. Lupus is difficult to diagnose, hard to live with and challenging to treat. Lupus has a range of symptoms often confused with other conditions, making it difficult to recognize and diagnose. Its symptoms and outcomes can be severe or fatal, its onset can be sudden, its causes are unclear and there is no known cure. This NOFO addresses several persisting gaps and inequities related to lupus. Lupus can result in a range of negative outcomes including disability, social stigma, lost productivity, absence from the workforce, reduction in quality of life, organ damage or failure or early death. Undiagnosed or late diagnosis of lupus can increase the likelihood or worsen the severity of many of these outcomes. Even with a correct diagnosis, lupus is challenging to treat. Much is needed to improve the care and quality of life for people living with the disease. The public health sector can contribute a great deal to this end and help mitigate these gaps and inequities. The purpose of the NOFO is to support national organizations implementing national efforts to help reduce time to lupus diagnoses, increase number of people with lupus getting needed care and ongoing treatment, improve lupus care, care transition and care coordination, improve lupus patients’ self-management behaviors, and improve quality of life and health outcomes among people with lupus. This NOFO will focus on two key strategies and their associated activities: Strategy: Increase awareness, knowledge and skills among healthcare providers to appropriately recognize the signs and symptoms of lupus, what to do if lupus is expected, and provide quality, well-coordinated lupus care. Activities are to: Develop and promote healthcare provider lupus training and education. Strategy: In collaboration with key stakeholders promote the national uptake and use of effective lupus self-management tools and/or services. Activities are to: Support implementation and evaluation of lupus-specific self-management tools and/or services. These strategies and activities are intended to result in the following outcome measures: Increased number of healthcare providers recognizing the signs and symptoms of lupus and what to do if lupus is expected. The NOFO will fund TWO awards, ONE award will be issued for each Strategy. Applicant can apply for one or both Strategies but must submit a separate application for each Strategy. A total of $2,670,230 is available for annual funding, a range of $1.1 Million to $1.5 Million will be awarded to each successful applicant. |
| Link to Additional Information: | – |
| Grantor Contact Information: | If you have difficulty accessing the full announcement electronically, please contact:
–
Email:mgk6@cdc.gov |
DISPLAYING: Forecast 2
General Information
| Document Type: | Grants Notice |
| Funding Opportunity Number: | CDC-RFA-DP20-2008 |
| Funding Opportunity Title: | Developing and Disseminating Strategies to Build Sustainable Lupus Awareness, Knowledge, Skills, and Partnerships |
| Opportunity Category: | Discretionary |
| Opportunity Category Explanation: | – |
| Funding Instrument Type: | Cooperative Agreement |
| Category of Funding Activity: | Health |
| Category Explanation: | – |
| Expected Number of Awards: | 2 |
| Assistance Listings: | 93.068 — Chronic Diseases: Research, Control, and Prevention |
| Cost Sharing or Matching Requirement: | No |
| Version: | Forecast 2 |
| Posted Date: | Apr 02, 2020 |
| Last Updated Date: | Apr 02, 2020 |
| Original Closing Date for Applications: | – |
| Current Closing Date for Applications: | – |
| Archive Date: | – |
| Estimated Total Program Funding: | $2,670,230 |
| Award Ceiling: | $1,500,000 |
| Award Floor: | $1,100,000 |
Eligibility
| Eligible Applicants: | Unrestricted (i.e., open to any type of entity above), subject to any clarification in text field entitled “Additional Information on Eligibility” |
| Additional Information on Eligibility: |
Additional Information
| Agency Name: | Centers for Disease Control – NCCDPHP |
| Description: | Lupus is a systemic autoimmune disease. It is estimated 161,000 to 322,000 Americans have the most common type of lupus, systemic lupus erythematosus (SLE). Although anyone can get lupus, 9 out of 10 diagnoses of lupus are in women ages 15 to 44. African American and Latino women are at greater risk for lupus than white women and usually get it at a younger age and have more severe symptoms. Lupus is also more common in Hispanic, Asian, and Native American and Alaskan Native women. The causes of lupus are unknown but are believed to be linked to genetic, environmental, and hormonal factors.Lupus is difficult to diagnose, hard to live with and challenging to treat. Lupus has a range of symptoms often confused with other conditions, making it difficult to recognize and diagnose. Its symptoms and outcomes can be severe or fatal, its onset can be sudden, its causes are unclear and there is no known cure.This NOFO addresses several persisting gaps and inequities related to lupus. Lupus can result in a range of negative outcomes including disability, social stigma, lost productivity, absence from the workforce, reduction in quality of life, organ damage or failure or early death. Undiagnosed or late diagnosis of lupus can increase the likelihood or worsen the severity of many of these outcomes. Even with a correct diagnosis, lupus is challenging to treat. Much is needed to improve the care and quality of life for people living with the disease. The public health sector can contribute a great deal to this end and help mitigate these gaps and inequities.The purpose of the NOFO is to support national organizations implementing national efforts to help reduce time to lupus diagnoses, increase number of people with lupus getting needed care and ongoing treatment, improve lupus care, care transition and care coordination, improve lupus patients’ self-management behaviors, and improve quality of life and health outcomes among people with lupus. This NOFO will focus on two key strategies and their associated activities:Strategy: Increase awareness, knowledge and skills among healthcare providers to appropriately recognize the signs and symptoms of lupus, what to do if lupus is expected, and provide quality, well-coordinated lupus care. Activities are to:Develop and promote healthcare provider lupus training and education.Increase the role of technology in the clinical setting.Collaborate with health professional associations to establish or increase sustainable educational opportunities.Develop and promote practice procedures for transition of lupus care from pediatric to adult care.Strategy: In collaboration with key stakeholders promote the national uptake and use of effective lupus self-management tools and/or services. Activities are to:Support implementation and evaluation of lupus-specific self-management tools and/or services.Promote the national uptake and use of lupus self-management tools and/or services among women ages 15 to 44 and key stakeholders.Apply electronic health or medical record systems or other medical information technology to help diagnose lupus, refer patients to appropriate clinical and lupus self-management tools/services, and track patient information and health outcomes.Identify and address lupus patients’ barriers to access effective lupus self-management tools and/or services.These strategies and activities are intended to result in the following outcome measures:Increased number of healthcare providers recognizing the signs and symptoms of lupus and what to do if lupus is expected.Increased number of healthcare providers using tele-health and/or electronic health records to identify lupus cases and treatment gaps.Increased number of settings receiving guidance on transition of pediatric lupus care to adult care.Increased number of people living with lupus engaged in the use of lupus self-management tools and/or services.Increased number of referrals to lupus self-management tools and/or services using electronic health or medical record systems or other medical information technology.Improved self-management behaviors among people with lupus.The NOFO will fund TWO awards, ONE award will be issued for each Strategy. Applicant can apply for one or both Strategies but must submit a separate application for each Strategy. A total of $2,670,230 is available for annual funding, a range of $1.1 Million to $1.5 Million will be awarded to each successful applicant. |
| Link to Additional Information: | – |
| Grantor Contact Information: | If you have difficulty accessing the full announcement electronically, please contact:
–
Email:mgk6@cdc.gov |
DISPLAYING: Forecast 1
General Information
| Document Type: | Grants Notice |
| Funding Opportunity Number: | CDC-RFA-DP20-2008 |
| Funding Opportunity Title: | Developing and Disseminating Strategies to Build Sustainable Lupus Awareness, Knowledge, Skills, and Partnerships |
| Opportunity Category: | Discretionary |
| Opportunity Category Explanation: | – |
| Funding Instrument Type: | Cooperative Agreement |
| Category of Funding Activity: | Health |
| Category Explanation: | – |
| Expected Number of Awards: | 2 |
| Assistance Listings: | 93.068 — Chronic Diseases: Research, Control, and Prevention |
| Cost Sharing or Matching Requirement: | No |
| Version: | Forecast 1 |
| Posted Date: | Apr 02, 2020 |
| Last Updated Date: | Apr 02, 2020 |
| Original Closing Date for Applications: | – |
| Current Closing Date for Applications: | – |
| Archive Date: | – |
| Estimated Total Program Funding: | $2,670,230 |
| Award Ceiling: | $1,500,000 |
| Award Floor: | $1,100,000 |
Eligibility
| Eligible Applicants: | Unrestricted (i.e., open to any type of entity above), subject to any clarification in text field entitled “Additional Information on Eligibility” |
| Additional Information on Eligibility: |
Additional Information
| Agency Name: | Centers for Disease Control – NCCDPHP |
| Description: | Lupus is a systemic autoimmune disease. It is estimated 161,000 to 322,000 Americans have the most common type of lupus, systemic lupus erythematosus (SLE). Although anyone can get lupus, 9 out of 10 diagnoses of lupus are in women ages 15 to 44. African American and Latino women are at greater risk for lupus than white women and usually get it at a younger age and have more severe symptoms. Lupus is also more common in Hispanic, Asian, and Native American and Alaskan Native women. The causes of lupus are unknown but are believed to be linked to genetic, environmental, and hormonal factors. Lupus is difficult to diagnose, hard to live with and challenging to treat. Lupus has a range of symptoms often confused with other conditions, making it difficult to recognize and diagnose. Its symptoms and outcomes can be severe or fatal, its onset can be sudden, its causes are unclear and there is no known cure. This NOFO addresses several persisting gaps and inequities related to lupus. Lupus can result in a range of negative outcomes including disability, social stigma, lost productivity, absence from the workforce, reduction in quality of life, organ damage or failure or early death. Undiagnosed or late diagnosis of lupus can increase the likelihood or worsen the severity of many of these outcomes. Even with a correct diagnosis, lupus is challenging to treat. Much is needed to improve the care and quality of life for people living with the disease. The public health sector can contribute a great deal to this end and help mitigate these gaps and inequities. The purpose of the NOFO is to support national organizations implementing national efforts to help reduce time to lupus diagnoses, increase number of people with lupus getting needed care and ongoing treatment, improve lupus care, care transition and care coordination, improve lupus patients’ self-management behaviors, and improve quality of life and health outcomes among people with lupus. This NOFO will focus on two key strategies and their associated activities: Strategy: Increase awareness, knowledge and skills among healthcare providers to appropriately recognize the signs and symptoms of lupus, what to do if lupus is expected, and provide quality, well-coordinated lupus care. Activities are to: Develop and promote healthcare provider lupus training and education. Strategy: In collaboration with key stakeholders promote the national uptake and use of effective lupus self-management tools and/or services. Activities are to: Support implementation and evaluation of lupus-specific self-management tools and/or services. These strategies and activities are intended to result in the following outcome measures: Increased number of healthcare providers recognizing the signs and symptoms of lupus and what to do if lupus is expected. The NOFO will fund TWO awards, ONE award will be issued for each Strategy. Applicant can apply for one or both Strategies but must submit a separate application for each Strategy. A total of $2,670,230 is available for annual funding, a range of $1.1 Million to $1.5 Million will be awarded to each successful applicant. |
| Link to Additional Information: | – |
| Grantor Contact Information: | If you have difficulty accessing the full announcement electronically, please contact:
–
Email:mgk6@cdc.gov |
Related Documents
Folder 325995 Full Announcement-FULL_ANNOUNCEMENT -> CDC-RFA-DP20-2008.pdf
Folder 325995 Full Announcement-FULL_ANNOUNCEMENT -> Full Announcement – CDC-RFA-DP20-2008 Developing and Disseminating Strategies to Build Sustainable Lupus Awareness, Knowledge, Skills, and Partnerships.pdf
Packages
| Agency Contact Information: | Margaret Kaniewski mgk6@cdc.gov Email: mgk6@cdc.gov |
| Who Can Apply: | Organization Applicants |
| Assistance Listing Number | Competition ID | Competition Title | Opportunity Package ID | Opening Date | Closing Date | Actions |
|---|---|---|---|---|---|---|
| 93.068 | CDC-RFA-DP20-2008 | Developing and Disseminating Strategies to Build Sustainable Lupus Awareness, Knowledge, Skills, and Partnerships | PKG00261349 | May 01, 2020 | Jun 26, 2020 | View |
Package 1
Mandatory forms
325995 SF424_2_1-2.1.pdf
325995 SFLLL_1_2-1.2.pdf
325995 SF424A-1.0.pdf
325995 BudgetNarrativeAttachments_1_2-1.2.pdf
325995 ProjectNarrativeAttachments_1_2-1.2.pdf
325995 HHS_CheckList_2_1-2.1.pdf
Optional forms
325995 OtherNarrativeAttachments_1_2-1.2.pdf
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