Notice of Intent to Publish a Funding Opportunity Announcement for HEAL Initiative: Sickle Cell Disease Pain Management Trials Utilizing the Pain Effectiveness Research Network Cooperative Agreement (UG3/UH3, Clinical Trial Required)
Notice Number:
NOT-AT-21-017

Key Dates

Release Date:
September 09, 2021
Estimated Publication Date of Funding Opportunity Announcement:
October 15, 2021
First Estimated Application Due Date:
December 15, 2021
Earliest Estimated Award Date:
September 01, 2022
Earliest Estimated Start Date:
September 01, 2022
Related Announcements

NOT-AT-21-018 - Notice of Intent to Publish a Funding Opportunity Announcement for HEAL Initiative: Pragmatic and Implementation Studies for the Management of Sickle Cell Disease Pain (UG3/UH3, Clinical Trials Optional)

Issued by

National Center for Complementary and Integrative Health (NCCIH)

National Heart, Lung, and Blood Institute (NHLBI)

National Institute on Drug Abuse (NIDA)

National Institute of Nursing Research (NINR)

National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)

National Institute on Minority Health and Health Disparities (NIMHD)

All applications to this funding opportunity announcement should fall within the mission of the Institutes/Centers. The following NIH Offices may co-fund applications assigned to those Institutes/Centers.

Office of Behavioral and Social Sciences Research (OBSSR)

Office of Research on Women's Health (ORWH)

Purpose

The National Institutes of Health (NIH) HEAL (Helping to End Addiction Long-termSM) Initiative intends to promote a new initiative by publishing a Funding Opportunity Announcement (FOA) soliciting applications to support multisite effectiveness clinical trials of multicomponent nonopioid pharmacologic and nonpharmacologic approaches for acute and/or chronic sickle cell disease (SCD) pain management. Trials supported under this initiative would also address the impact of these approaches on related psychological and functional outcomes to support improved overall well-being and quality of life. In addition, studies that address stigma, structural health care system, and social factors that may hinder quality comprehensive pain care for patients with SCD are also of interest. Investigators are encouraged to include the collection of well-justified biological markers or psychological processes that have demonstrated that they mediate pain outcomes. Trials should collect sufficient measures to phenotype participants including type of pain, variability of pain, co-occurring conditions, and social determinants of health. The studies must address questions within the mission and research interests of the NIH HEAL Initiative and evaluate preventive or treatment strategies or interventions including medications, biologics, procedures, medical and assistive devices and technologies, behavioral interventions, rehabilitation strategies, complementary interventions, integrated approaches, and delivery system strategies in well controlled trials in patients with SCD to manage acute and/or chronic pain. The overall goal is to inform clinicians about the effectiveness of coordinated, multidisciplinary management strategies that reduce acute and/or chronic SCD pain and that continue to provide access to opioid pain management when needed. Clinical trials will be conducted within the infrastructure of the HEAL Pain Effectiveness Research Network which has dedicated pain and clinical trial design expertise.

The purpose of this Notice is to allow potential applicants sufficient time to develop meaningful collaborations among investigators with expertise in SCD, pain, health disparities, psychosocial research, and clinicians. It will also allow potential applicants sufficient time to develop responsive projects.

The FOA is expected to be published in Fall 2021, with an expected application due date in Winter 2021.

This FOA will utilize the UG3/UH3 activity code, a bi-phasic, milestone-driven cooperative agreement. The UG3 phase will provide funding for a one-year planning phase. The second, UH3 phase will provide up to four years of funding for clinical trial implementation. Transition from the UG3 to the UH3 will depend on successful completion of milestones established for the UG3. Applications must address planned activities for both the UG3 and UH3 phases.

Details of the planned FOA are provided below.

Research Initiative Details

This effort is part of the NIH HEAL (Helping to End Addiction Long-termSM) Initiative to speed the development and implementation of scientific solutions to the national opioid public health crisis. The NIH HEAL InitiativeSMwill bolster research across NIH to (1) improve treatment and prevention of opioid misuse and opioid use disorder and (2) enhance pain management. More information and periodic updates about the Initiative are available at: https://heal.nih.gov/.

The most common complication of SCD is pain, including severe acute pain episodes primarily from vaso-occlusive crises, chronic persistent pain, and neuropathic pain. SCD pain symptoms span from childhood through adulthood and contribute to high rates of hospitalizations, emergency room visits, poor functional and psychosocial outcomes, and an increased rate of mortality. Management of acute and chronic pain among individuals with SCD is complex and often includes treatment such as opioid-based therapies which do not always address other co-occurring symptoms that may exacerbate pain, such as sleep disturbances, stress, anxiety, depression, and increased risk of opioid addiction. Even after curative SCD therapy, severe chronic pain continues for a significant proportion of individuals.

Further, the SCD population primarily comprises racial and ethnic minorities who experience disparities in receiving quality comprehensive care for SCD, including pain management. These disparities have been linked to the stigma associated with this disease as well as social factors such as racism and socioeconomic status. In turn this stigma associated with SCD impacts health outcomes, health seeking behavior, and patient-provider interactions. Indeed, recent reports from the National Academy of Sciences and the Pain Management Best Practices Inter-Agency Task Force highlight the need for a paradigm shift to provide comprehensive care delivery models for managing pain and improving the overall well-being and quality of life of individuals with SCD associated pain. To address these combined challenges, a biopsychosocial approach to pain management that includes a multidisciplinary approach that addresses biological, psychological, and social influences on pain provides an opportunity to treat the whole person, improve overall health status, and possibly mitigate some of the factors leading to the stigma associated with SCD.

While opioid therapy remains vital for the current management of acute SCD pain, non-opioid pharmacologic and nonpharmacologic approaches for pain management have been deemed feasible and of interest to individuals with SCD. Research is needed to enhance the evidence base regarding the effectiveness of multicomponent non-opioid pharmacologic and nonpharmacologic approaches for acute and chronic SCD pain management approaches to reduce different SCD pain types, improve related psychological and functional outcomes, and reduce reliance on opioid-based treatments.

This initiative will encourage UG3/UH3 phased cooperative research applications to support multisite clinical trials to test the effectiveness of multicomponent nonopioid pharmacologic and nonpharmacologic approaches for acute and/or chronic SCD pain management. Effectiveness trials may include or allow continuation of opioid medication use if appropriate, however opioid medication use alone should not be the only intervention studied. Trials supported in this initiative also should address the impact of these approaches on related psychological and functional outcomes to support improved overall well-being and quality of life. Trials may also address stigma, structural health care system, and social factors that may hinder quality comprehensive care. Applicants are encouraged to include participants across the lifespan including children, emerging adults, and adult populations, as appropriate. Clinical trials will be conducted within the infrastructure of the HEAL Pain Effectiveness Research Network which has dedicated pain and clinical trial design expertise. Multi-site trials will require participation of two or more clinical sites for completion of the study (e.g., in order to increase sample size, accelerate recruitment, or increase sample diversity and representation).

See companion Notice (NOT-AT-21-018) for details on a planned HEAL Initiative to support embedded pragmatic trials or implementation studies to evaluate the impact of health care system changes to improve adherence to evidence-based non-opioid pharmacologic and nonpharmacologic approaches for acute and chronic SCD pain management.

Funding Information
Estimated Total Funding

Up to $1,500,000 direct costs

Expected Number of Awards

Minimum of 3 awards pending availability of funds and receipt of meritorious applications

Estimated Award Ceiling

The application budget for the one-year UG3 phase is limited to $500,000 in direct costs. Costs for each year of the UH3 phase are limited to $1 million in direct costs. The maximum period of funding for the UG3 phase is one year and the maximum period of funding of the UH3 phase is four years, for a total of five years for the entire UG3/UH3 award.

Primary Assistance Listing Number(s)

93.213

Anticipated Eligible Organizations
Public/State Controlled Institution of Higher Education
Private Institution of Higher Education
Nonprofit with 501(c)(3) IRS Status (Other than Institution of Higher Education)
Small Business
For-Profit Organization (Other than Small Business)
State Government
Indian/Native American Tribal Government (Federally Recognized)
County governments
Independent school districts
Public housing authorities/Indian housing authorities
Indian/Native American Tribally Designated Organization (Native American tribal organizations (other than Federally recognized tribal governments)
U.S. Territory or Possession
Indian/Native American Tribal Government (Other than Federally Recognized)
Regional Organization
Eligible Agencies of the Federal Government

Applications are not being solicited at this time.

Inquiries

Please direct all inquiries to:

Della White, Ph.D.

National Center for Complementary and Integrative Health (NCCIH)

301-827-6358

della.white@nih.gov


Weekly TOC for this Announcement
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