Opportunity Information: Apply for HRSA 15 079

  • The Health Resources and Services Administration in the health sector is offering a public funding opportunity titled "Cooperative Agreements to Support Comprehensive Medical Care for Thalassemia" and is now available to receive applicants.
  • Interested and eligible applicants and submit their applications by referencing the CFDA number(s): 93.110 Maternal and Child Health Federal Consolidated Programs.
  • This funding opportunity was created on Dec 23, 2014 and posted on Dec 23, 2014.
  • Applicants must submit their applications by Feb 23, 2015. (Agency may still review applications by suitable applicants for the remaining/unused allocated funding in 2026.)
  • The funding agency has allocated a total of $615,000.00 to eligible and selected applicants.
  • The number of recipients for this funding is limited to 4 candidate(s).
  • Eligible applicants include: Others (see text field entitled Additional Information on Eligibility for clarification) Native American tribal organizations (other than Federally recognized tribal governments).
  • As cited in 42 CFR Part 51 a.3(a), any public or private entity, including an Indian Tribe or Tribal organization (as those terms are defined in 25 U.S.C. 450b), is eligible to apply for this Federal funding opportunity. Applicants are not allowed to apply for both Projects.
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Opportunity Summary:

The Health Resources and Services Administration (HRSA), through the Maternal and Child Health Bureau (MCHB), offered a discretionary cooperative agreement opportunity (HRSA-15-079) to strengthen comprehensive medical care for people with thalassemia under the National Hereditary Blood Disorders Programs authority in section 501(a)(2) of the Social Security Act (42 U.S.C. 701(a)(2)). The central purpose was a time-limited demonstration project aimed at two practical outcomes: improving how individuals with thalassemia are identified and improving their access to high-quality medical services, especially for those who require ongoing treatment such as transfusion management and related complication monitoring.

The program was built around coordinated work between regionally focused awardees and one national-level partner. Together, awardees were expected to develop and sustain a national approach to understanding who is affected by thalassemia and what services they need, with the broader intent of assuring access to comprehensive care. A major deliverable was collaboration with stakeholders to propose a model protocol for improving thalassemia care delivery, including guidance on transfusion therapy, disease-specific screening practices, and consistent monitoring and treatment of therapy-related side effects, particularly iron overload. Beyond clinical protocols, the opportunity emphasized access: expanding specialty provider availability for thalassemia patients through strategies such as thalassemia treatment center networks, telehealth, and other coordinated referral and network models. It also highlighted the importance of primary care access so that patients can receive routine, non-disease-specific care (general health needs) alongside specialty hematology services.

Applicants had to choose one of two distinct projects and could not apply to both. Project 1, the Thalassemia Regionalized Collaborative Approach, was designed to fund up to three organizations to lead regional collaborative efforts that improve thalassemia care. HRSA expected to make roughly $540,000 available per year for Project 1 in total, with an application ceiling of up to $180,000 per awardee per year. Project 2, the National Level Partner, was intended to fund a single organization to support national coordination and partnership functions, with about $75,000 available per year and a ceiling of up to $75,000 per year. Both Project 1 and Project 2 were cooperative agreements, meaning HRSA anticipated substantial federal involvement and ongoing collaboration with recipients rather than a purely hands-off grant structure. Each project had a two-year project period.

Eligibility was broad: under 42 CFR Part 51a.3(a), any public or private entity could apply, including Indian Tribes or Tribal organizations as defined in 25 U.S.C. 450b, and other eligible applicants as described in the funding notice. There was no cost sharing or matching requirement. The opportunity was posted on December 23, 2014, with an original and current closing date of February 23, 2015, and it was later archived on April 24, 2015. HRSA anticipated making four total awards across both projects, with an estimated total funding amount of $615,000.

For administrative reference, the opportunity fell under CFDA 93.110 (Maternal and Child Health Federal Consolidated Programs) and used the cooperative agreement funding instrument within the health activity category. The funding announcement listed HRSA Grants Application Center support and provided a program contact, Edward Donnell Ivy, M.D., M.P.H., for questions about the announcement and access to materials.

Frequently Asked Questions (FAQs)

What is this funding opportunity?

This opportunity was a discretionary cooperative agreement from the Health Resources and Services Administration (HRSA), through the Maternal and Child Health Bureau (MCHB), under the National Hereditary Blood Disorders Programs authority (section 501(a)(2) of the Social Security Act, 42 U.S.C. 701(a)(2)). It was identified as HRSA-15-079 and focused on strengthening comprehensive medical care for people with thalassemia.

What was the main purpose of HRSA-15-079?

The central purpose was a time-limited demonstration project aimed at two practical outcomes: (1) improving how individuals with thalassemia are identified, and (2) improving access to high-quality medical services, especially for people who require ongoing treatment such as transfusion management and monitoring for complications.

What outcomes did HRSA want the program to achieve?

The program emphasized improving identification of individuals with thalassemia and improving access to comprehensive, high-quality medical care. It particularly highlighted ongoing treatment needs (for example, transfusion therapy) and related complication monitoring (for example, therapy-related side effects such as iron overload).

What is meant by a "time-limited demonstration project" in this announcement?

In this context, it refers to a project designed to operate for a defined period (a two-year project period) to demonstrate practical improvements in thalassemia identification and access to comprehensive care, rather than an open-ended, indefinite program.

How was the program structured (regional and national roles)?

The program was built around coordinated work between regionally focused awardees and one national-level partner. Together, awardees were expected to develop and sustain a national approach to understanding who is affected by thalassemia and what services they need, with the broader intent of assuring access to comprehensive care.

What was a major deliverable expected from awardees?

A major deliverable was collaboration with stakeholders to propose a model protocol for improving thalassemia care delivery. This included guidance on transfusion therapy, disease-specific screening practices, and consistent monitoring and treatment of therapy-related side effects, particularly iron overload.

Did the opportunity address both specialty and primary care access?

Yes. In addition to strengthening specialty thalassemia services (such as hematology and transfusion management), the opportunity also highlighted the importance of primary care access so that patients can receive routine, non-disease-specific care alongside specialty services.

What strategies were encouraged to expand access to thalassemia specialty care?

The announcement emphasized expanding specialty provider availability through strategies such as thalassemia treatment center networks, telehealth, and other coordinated referral and network models.

What were the two project options applicants could choose from?

Applicants had to choose one of two distinct projects:

  • Project 1: Thalassemia Regionalized Collaborative Approach (regional collaborative efforts to improve thalassemia care)
  • Project 2: National Level Partner (national coordination and partnership functions)

Could an organization apply for both Project 1 and Project 2?

No. Applicants had to choose one of the two projects and could not apply to both.

How many awards were expected under Project 1?

Project 1 was designed to fund up to three organizations to lead regional collaborative efforts that improve thalassemia care.

How much funding was available for Project 1?

HRSA expected to make roughly $540,000 available per year for Project 1 in total, with an application ceiling of up to $180,000 per awardee per year.

How many awards were expected under Project 2?

Project 2 was intended to fund a single organization to serve as the National Level Partner.

How much funding was available for Project 2?

About $75,000 per year was available for Project 2, with a ceiling of up to $75,000 per year.

What is the total estimated funding and number of awards for the entire opportunity?

HRSA anticipated making four total awards across both projects, with an estimated total funding amount of $615,000.

What type of funding instrument was used?

Both Project 1 and Project 2 used a cooperative agreement funding instrument.

What does it mean that these awards were "cooperative agreements"?

It means HRSA anticipated substantial federal involvement and ongoing collaboration with recipients, rather than a purely hands-off grant structure.

How long was the project period?

Each project had a two-year project period.

Who was eligible to apply?

Eligibility was broad. Under 42 CFR Part 51a.3(a), any public or private entity could apply, including Indian Tribes or Tribal organizations as defined in 25 U.S.C. 450b, and other eligible applicants as described in the funding notice.

Was cost sharing or matching required?

No. There was no cost sharing or matching requirement.

When was the opportunity posted and when did it close?

The opportunity was posted on December 23, 2014. The original and current closing date was February 23, 2015.

Is this funding opportunity still open?

No. It was later archived on April 24, 2015.

What is the CFDA number associated with this opportunity?

The opportunity fell under CFDA 93.110 (Maternal and Child Health Federal Consolidated Programs).

What federal agency and bureau administered this opportunity?

The opportunity was administered by HRSA, through the Maternal and Child Health Bureau (MCHB).

What activity category did this opportunity fall under?

The funding instrument was a cooperative agreement within the health activity category.

Who could applicants contact with questions about the announcement?

The announcement listed a program contact for questions about the announcement and access to materials: Edward Donnell Ivy, M.D., M.P.H.

Was there application support mentioned?

Yes. The funding announcement listed HRSA Grants Application Center support.

What kinds of clinical issues were specifically highlighted for thalassemia care improvement?

The opportunity specifically highlighted guidance on transfusion therapy, disease-specific screening practices, and consistent monitoring and treatment of therapy-related side effects, particularly iron overload.

What was the broader intent beyond developing clinical protocols?

Beyond clinical protocols, the opportunity emphasized access to care: developing approaches that assure access to comprehensive services and improving availability of specialty providers and coordinated care models for thalassemia patients.

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