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Joe Selby MD, MPH
PCORI Executive Director
8th Annual Weitzman Symposium
Community Health Center, Inc
May 16, 2013
Transforming Health Care
Source: Affordable Care Act. Subtitle D—Patient-Centered Outcomes Research.
PUBLIC LAW 111–148—MAR. 23, 2010.
“The purpose of the Institute is to assist
patients, clinicians, purchasers, and policy-
makers in making informed health
decisions by advancing the quality and
relevance of evidence concerning the manner
in which diseases, disorders, and other health
conditions can effectively and appropriately be
prevented, diagnosed, treated, monitored, and
managed through research and evidence
synthesis that considers variations in patient
subpopulations and the dissemination of
research findings with respect to the relative
health outcomes, clinical effectiveness, and
appropriateness of medical treatments,
services.
Purpose
Of
PCORI
PCORI’s Broad Mandate
3
PCORI’s Board of Governors
P3
PCORI Board of Governors, March 2012 in Baltimore, MD
4
What Does PCORI Mean By Patient-
Centeredness?
Does the proposed research compare
treatment options that matter to patients; are
these realistic choices faced by patients or
other decision-makers?
Does the research focus on outcomes of
interest to patients and their caregivers,
including health, health-related quality of life,
function, symptoms, safety from medical
harm, survival and satisfaction with care?
5
PCORI’s Mission – Through Engagement
Mission
The Patient-Centered Outcomes Research Institute
(PCORI) helps people make informed health care
decisions, and improves health care delivery and
outcomes, by producing and promoting high integrity,
evidence-based information that comes from research
guided by patients, caregivers and the broader health
care community.
5www.pcori.org
6
PCORI’s Rationale for Engagement
Advise Us on what PCORI
Should Study:
Tell Us How We Are Doing
Review Proposals and
Partner in Research
Help Us Share the Findings
Patients
and
Stakeholders
• Topic generation
• Research prioritization
 Merit Review
 Participate in research
How can we improve on what we
are doing and how we are doing
it?
 Dissemination
7
PCORI Review Criteria
1.
Impact of the condition on the health of
individuals and populations –
burden in terms of prevalence, suffering, costs
2.
Potential for the study to improve healthcare and
outcomes –
likelihood that this study’s findings could change current practice
3. Technical merit –
research plan, analytic methods, research team, environment
4.
Patient-Centeredness -
relevance of the study question and the outcomes to patients
5.
Patient and stakeholder engagement –
inclusion of relevant patients and stakeholders on research team
8
PCORI Funding – Approximate
2012
2013
2014
2015
....
2019
$150,000,000*
$300,000,000
$500,000,000
$500,000,000
$500,000,000
* 20% each year goes to AHRQ/HHS 8
9
PCORI’s National Priorities and Research
Agenda
9
Assessment of Prevention, Diagnosis, Treatment Options
• Comparisons of alternative clinical options; identifying patient differences in response to
therapy; studies of patient preferences for various outcomes
Improving Healthcare Systems
• Improving system support of patient self-management, coordination of care for complex
conditions, access to care; comparing alternative strategies for workforce deployment.
Communication & Dissemination Research
• Understanding and enhancing shared decision-making; alternative strategies for
dissemination of evidence; exploring opportunities to improve patient health literacy
Addressing Disparities
• Understanding differences in effectiveness across groups; understanding differences in
preferences across groups; reducing disparities through use of findings from PCOR
Accelerating PCOR and Methodological Research
• Improving study designs and analytic methods of PCOR; building and improving clinical
data networks
10
Improving Healthcare Systems –
from PCORI’s Funding Announcement
10
Research that compares alternative system-level approaches to improving:
- patients’ access to care;
- receipt of appropriate evidence-based care;
- quality of care;
- decision-making based on personal values;
- coordination of care across healthcare settings,
the efficiency of healthcare delivery.
Strategies of interest include, but are not limited to:
novel applications of health information systems,
incentives directed at clinicians, patients and systems;
payment reforms, such as value-based purchasing, bundled
payments and accountable care organizations;
reconfigurations (redesign) of care, such as the patient-centered
medical home;
new and extended roles for allied health professionals
11
Addressing Health Disparities –
from PCORI’s Funding Announcement
11
Research that compares:
Interventions to reduce or eliminate disparities in patient-centered outcomes,
including health, healthcare, and patient-reported outcomes.
practices that address contextual factors such as socioeconomic, demographic,
or community factors and their impact on patient-centered health outcomes.
benefits and risks of treatment, diagnostic, prevention, or service
options across different patient populations.
strategies to overcome patient, provider, or systems level barriers (e.g.,
language, culture, transportation, homelessness, unemployment, lack of
family/caregiver support)
best practices within various patient populations for information sharing and
shared decision-making.
 Addresses practical questions – especially those of interest
to patients and providers – usually head-to-head
comparisons
 Conducted in ―typical‖ patients and ―typical‖ care delivery
settings
 Considers the full range of outcomes of interest to patients
and clinicians
 Considers possible differences in treatment effectiveness in
patient subgroups – what works for whom?
 May be RCTs or observational studies
 But NOT cost-effectiveness or cost comparison studies
Comparative Clinical Effectiveness Research
– PCORI Style
13
PCORI’s Broad Solicitations for Research Funding
13
#1: Investigator-Generated Pathway – ―BROAD‖
Diverse portfolio addressing
high-priority questions
PCORI Projects Involving CHC’s
14
• Pilot Project: Tucson, Arizona
Integrating and Comparing Community-Based
Participatory and Conjoint Analysis
• Pilot Project: Los Angeles, California
A Modified Delphi Approach to Defining a Patient-
Centered Community Health Center
• Pilot Project: Boston, Massachusetts
Developing an Analytic Tool to Assess Patient
Responses
• Addressing Disparities Cycle I: Tuscaloosa, Alabama
Reducing Disparities with Literacy-Adapted
Psychosocial Treatments for Chronic Pain
A Modified Delphi Approach to Defining a Patient-
Centered Community Health Center (Pilot Project)
15
Primary Investigator and Institution: Robin Clarke, MD
University of California, Los Angeles
Award Amount: $307,985
Description: Evaluates the theories, evidence, and practices of enabling services, such
as providing transportation to appointments, conducting case management
assessments, or performing community outreach. Goals of the study are to:
 Define a specific standard of care for each category of enabling service that will
facilitate active investigation of how these patient-centered services affect the
health care delivered to underserved patients.
 Improve the implementation, diffusion, and reimbursement of enabling services.
 Reshape how the existing patient-centered medical home paradigm applies to
practices caring for low-income patients.
Featured Project Strength:
 Creates a new research method that incorporates community health
center providers and patients to define what the standards of care are for
these services.
 Addresses barriers to care that affect approximately 25 million
Americans.
Engaging Stakeholders to Improve Depression
Management in a Tribal Health System (Pilot Project)
16
Primary Investigator and Institution: Renee Robinson, PharmD,
Southcentral Foundation
Award Amount: $604,301
Description: Project will develop, test, and refine a tool to support decision making
within a tribally-owned health care organization, using depression as example condition.
There are three specific aims:
 Identify stakeholder preferences and needs that influence depression treatment
decisions in Alaska Native and American Indian people.
 Develop a tool to help translate and integrate evidence-based guidelines, and
stakeholder preferences and needs into depression management decisions.
 Determine impact of the stakeholder-centered tool on health, service utilization, and
outcomes.
Featured Project Strengths:
 Studies an issue with high prevalence in an underserved community.
 The results will be applicable to other chronic health concerns, and other
racially and ethnically diverse populations with persistent health
disparities.
17
Cycle I Awards
17
• Assessment of Prevention, Diagnosis and Treatment Options: Ann Arbor, Michigan
Selection of Peritoneal Dialysis or Hemodialysis for Kidney
Failure: Gaining Meaningful Information for Patients and
Caregivers
• Communication and Dissemination Research: Jacksonville, Florida
Shared Medical Decision Making in Pediatric Diabetes
• Communications and Dissemination Research: University Heights, Iowa
Extension Connection: Advancing Dementia Care for
Rural and Hispanic Populations
• Assessment of Prevention, Diagnosis and Treatment Options: Rochester, Minnesota
Shared Decision Making in the Emergency Department:
The Chest Pain Choice Trial
18
Reducing Health Disparities in Appalachians with
Multiple Cardiovascular Disease Risk Factors
18
Primary Investigator and Institution: Debra Moser, DNSc, RN, FAAN
Kentucky University
Award Amount: $2,092,473.60
Description: Compares the effects of two approaches in reducing risk of
cardiovascular disease. Comparison is between the current standard of care
and the standard of care supplemented by culturally appropriate self-care tools.
 Examines four-month and one year impact of various measures, including tobacco
use, blood pressure, BMI, and the number of recruited people who stay with the
program.
 Study involves 300 individuals from Appalachian Kentucky who do not have a
primary care provider, and otherwise are not able to receive the standard of care
without intercession, and are at risk by having two or more modifiable risk factors.
factors.
Featured Project Strengths:
 This study will have a substantial impact on cardiovascular health
because it will provide needed patient-centered risk reduction to a major
at-risk population living in an environment where risk reduction is difficult.
 The potential for application to other environments and high-risk
populations is high.
Debra Moser
19
Creating a Clinic-Community Liaison Role in Primary
Care: Engaging Patients and Community in Health Care
Innovation
19
Primary Investigator and Institution: Clarissa Hsu, PhD
Group Health Cooperative
Award Amount: $1,564,384
Projected Completion Date: December 31, 2015
Description: Works with patients to design role for a clinic-community
liaison to link healthcare clinics with community. Strategy aims to increase
patients’ ability get what they need from both their community and their healthcare. The
specific goals are to:
 Create new ways to involve patients in designing their own healthcare by
developing processes and tools to help patients contribute ideas for how care
should be designed.
 Design and test a new clinic-community liaison role for primary care teams by
focusing on the prevention and treatment of chronic conditions.
Featured Project Strengths:
 This project follows up on an extremely promising intervention, drawing
upon existing data and methodologies.
 It is highly patient centered and focused on "real-world" perspective.
Clarissa Hsu
20
Location of PCORI’s First 104 Awards
20
Total: 124
2121
PCORI Engagement Awards
22
Purpose
Build community
Form or strengthen reciprocal relationships between
researchers and non-research communities
Support capacity building, co- learning, and the development of
a sustainable infrastructure to facilitate ―research done
differently‖
Accelerate proposal submission (or re-submission)
22
23
PCORI Engagement Awards – coming July
2013
Proposed by participants at October 2012 Transforming
Patient-Centered Research patient engagement workshop
Intended to provide resources to non–research entities for
community development, capacity building, or for
infrastructure development for engagement in research as
partners.
23
24
Design
24
25
Pre-Engagement/Community-Building Projects
(Up to $15,000 for 6 months)
Available to individuals,
consumer/patient organizations,
clinician(s) or researcher(s) or a
combination of the above to
support:
 Community building
 Creation of structure and
communication strategies
 Develop an understanding of
PCORI, and ―research done
differently‖
25
26
Partnership and Infrastructure Development
Projects (Up to $30,000 for 1 year)
Available to emerging
research/non-research
partnerships to support:
 Data network development
 Development of infrastructure
 Generation of research
questions through community
events, town hall meetings, etc.
 Minimum 50% of funds go to
non research partner(s)
26
27
Proposal Development Projects
(Up to $50,000 for 1 year)
Available to advanced
research/non-research
partnerships- including those who
submitted PCORI proposals and
were not funded - to support:
 PCORI research proposal
(re)submission
 Research partnership skill
development
 Minimum 50% of funds go to non
research partner(s)
27
28
Connect with PCORI
www.pcori.org
28

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PCORI's Broad Mandate and Patient-Centered Approach

  • 1. Joe Selby MD, MPH PCORI Executive Director 8th Annual Weitzman Symposium Community Health Center, Inc May 16, 2013 Transforming Health Care
  • 2. Source: Affordable Care Act. Subtitle D—Patient-Centered Outcomes Research. PUBLIC LAW 111–148—MAR. 23, 2010. “The purpose of the Institute is to assist patients, clinicians, purchasers, and policy- makers in making informed health decisions by advancing the quality and relevance of evidence concerning the manner in which diseases, disorders, and other health conditions can effectively and appropriately be prevented, diagnosed, treated, monitored, and managed through research and evidence synthesis that considers variations in patient subpopulations and the dissemination of research findings with respect to the relative health outcomes, clinical effectiveness, and appropriateness of medical treatments, services. Purpose Of PCORI PCORI’s Broad Mandate
  • 3. 3 PCORI’s Board of Governors P3 PCORI Board of Governors, March 2012 in Baltimore, MD
  • 4. 4 What Does PCORI Mean By Patient- Centeredness? Does the proposed research compare treatment options that matter to patients; are these realistic choices faced by patients or other decision-makers? Does the research focus on outcomes of interest to patients and their caregivers, including health, health-related quality of life, function, symptoms, safety from medical harm, survival and satisfaction with care?
  • 5. 5 PCORI’s Mission – Through Engagement Mission The Patient-Centered Outcomes Research Institute (PCORI) helps people make informed health care decisions, and improves health care delivery and outcomes, by producing and promoting high integrity, evidence-based information that comes from research guided by patients, caregivers and the broader health care community. 5www.pcori.org
  • 6. 6 PCORI’s Rationale for Engagement Advise Us on what PCORI Should Study: Tell Us How We Are Doing Review Proposals and Partner in Research Help Us Share the Findings Patients and Stakeholders • Topic generation • Research prioritization  Merit Review  Participate in research How can we improve on what we are doing and how we are doing it?  Dissemination
  • 7. 7 PCORI Review Criteria 1. Impact of the condition on the health of individuals and populations – burden in terms of prevalence, suffering, costs 2. Potential for the study to improve healthcare and outcomes – likelihood that this study’s findings could change current practice 3. Technical merit – research plan, analytic methods, research team, environment 4. Patient-Centeredness - relevance of the study question and the outcomes to patients 5. Patient and stakeholder engagement – inclusion of relevant patients and stakeholders on research team
  • 8. 8 PCORI Funding – Approximate 2012 2013 2014 2015 .... 2019 $150,000,000* $300,000,000 $500,000,000 $500,000,000 $500,000,000 * 20% each year goes to AHRQ/HHS 8
  • 9. 9 PCORI’s National Priorities and Research Agenda 9 Assessment of Prevention, Diagnosis, Treatment Options • Comparisons of alternative clinical options; identifying patient differences in response to therapy; studies of patient preferences for various outcomes Improving Healthcare Systems • Improving system support of patient self-management, coordination of care for complex conditions, access to care; comparing alternative strategies for workforce deployment. Communication & Dissemination Research • Understanding and enhancing shared decision-making; alternative strategies for dissemination of evidence; exploring opportunities to improve patient health literacy Addressing Disparities • Understanding differences in effectiveness across groups; understanding differences in preferences across groups; reducing disparities through use of findings from PCOR Accelerating PCOR and Methodological Research • Improving study designs and analytic methods of PCOR; building and improving clinical data networks
  • 10. 10 Improving Healthcare Systems – from PCORI’s Funding Announcement 10 Research that compares alternative system-level approaches to improving: - patients’ access to care; - receipt of appropriate evidence-based care; - quality of care; - decision-making based on personal values; - coordination of care across healthcare settings, the efficiency of healthcare delivery. Strategies of interest include, but are not limited to: novel applications of health information systems, incentives directed at clinicians, patients and systems; payment reforms, such as value-based purchasing, bundled payments and accountable care organizations; reconfigurations (redesign) of care, such as the patient-centered medical home; new and extended roles for allied health professionals
  • 11. 11 Addressing Health Disparities – from PCORI’s Funding Announcement 11 Research that compares: Interventions to reduce or eliminate disparities in patient-centered outcomes, including health, healthcare, and patient-reported outcomes. practices that address contextual factors such as socioeconomic, demographic, or community factors and their impact on patient-centered health outcomes. benefits and risks of treatment, diagnostic, prevention, or service options across different patient populations. strategies to overcome patient, provider, or systems level barriers (e.g., language, culture, transportation, homelessness, unemployment, lack of family/caregiver support) best practices within various patient populations for information sharing and shared decision-making.
  • 12.  Addresses practical questions – especially those of interest to patients and providers – usually head-to-head comparisons  Conducted in ―typical‖ patients and ―typical‖ care delivery settings  Considers the full range of outcomes of interest to patients and clinicians  Considers possible differences in treatment effectiveness in patient subgroups – what works for whom?  May be RCTs or observational studies  But NOT cost-effectiveness or cost comparison studies Comparative Clinical Effectiveness Research – PCORI Style
  • 13. 13 PCORI’s Broad Solicitations for Research Funding 13 #1: Investigator-Generated Pathway – ―BROAD‖ Diverse portfolio addressing high-priority questions
  • 14. PCORI Projects Involving CHC’s 14 • Pilot Project: Tucson, Arizona Integrating and Comparing Community-Based Participatory and Conjoint Analysis • Pilot Project: Los Angeles, California A Modified Delphi Approach to Defining a Patient- Centered Community Health Center • Pilot Project: Boston, Massachusetts Developing an Analytic Tool to Assess Patient Responses • Addressing Disparities Cycle I: Tuscaloosa, Alabama Reducing Disparities with Literacy-Adapted Psychosocial Treatments for Chronic Pain
  • 15. A Modified Delphi Approach to Defining a Patient- Centered Community Health Center (Pilot Project) 15 Primary Investigator and Institution: Robin Clarke, MD University of California, Los Angeles Award Amount: $307,985 Description: Evaluates the theories, evidence, and practices of enabling services, such as providing transportation to appointments, conducting case management assessments, or performing community outreach. Goals of the study are to:  Define a specific standard of care for each category of enabling service that will facilitate active investigation of how these patient-centered services affect the health care delivered to underserved patients.  Improve the implementation, diffusion, and reimbursement of enabling services.  Reshape how the existing patient-centered medical home paradigm applies to practices caring for low-income patients. Featured Project Strength:  Creates a new research method that incorporates community health center providers and patients to define what the standards of care are for these services.  Addresses barriers to care that affect approximately 25 million Americans.
  • 16. Engaging Stakeholders to Improve Depression Management in a Tribal Health System (Pilot Project) 16 Primary Investigator and Institution: Renee Robinson, PharmD, Southcentral Foundation Award Amount: $604,301 Description: Project will develop, test, and refine a tool to support decision making within a tribally-owned health care organization, using depression as example condition. There are three specific aims:  Identify stakeholder preferences and needs that influence depression treatment decisions in Alaska Native and American Indian people.  Develop a tool to help translate and integrate evidence-based guidelines, and stakeholder preferences and needs into depression management decisions.  Determine impact of the stakeholder-centered tool on health, service utilization, and outcomes. Featured Project Strengths:  Studies an issue with high prevalence in an underserved community.  The results will be applicable to other chronic health concerns, and other racially and ethnically diverse populations with persistent health disparities.
  • 17. 17 Cycle I Awards 17 • Assessment of Prevention, Diagnosis and Treatment Options: Ann Arbor, Michigan Selection of Peritoneal Dialysis or Hemodialysis for Kidney Failure: Gaining Meaningful Information for Patients and Caregivers • Communication and Dissemination Research: Jacksonville, Florida Shared Medical Decision Making in Pediatric Diabetes • Communications and Dissemination Research: University Heights, Iowa Extension Connection: Advancing Dementia Care for Rural and Hispanic Populations • Assessment of Prevention, Diagnosis and Treatment Options: Rochester, Minnesota Shared Decision Making in the Emergency Department: The Chest Pain Choice Trial
  • 18. 18 Reducing Health Disparities in Appalachians with Multiple Cardiovascular Disease Risk Factors 18 Primary Investigator and Institution: Debra Moser, DNSc, RN, FAAN Kentucky University Award Amount: $2,092,473.60 Description: Compares the effects of two approaches in reducing risk of cardiovascular disease. Comparison is between the current standard of care and the standard of care supplemented by culturally appropriate self-care tools.  Examines four-month and one year impact of various measures, including tobacco use, blood pressure, BMI, and the number of recruited people who stay with the program.  Study involves 300 individuals from Appalachian Kentucky who do not have a primary care provider, and otherwise are not able to receive the standard of care without intercession, and are at risk by having two or more modifiable risk factors. factors. Featured Project Strengths:  This study will have a substantial impact on cardiovascular health because it will provide needed patient-centered risk reduction to a major at-risk population living in an environment where risk reduction is difficult.  The potential for application to other environments and high-risk populations is high. Debra Moser
  • 19. 19 Creating a Clinic-Community Liaison Role in Primary Care: Engaging Patients and Community in Health Care Innovation 19 Primary Investigator and Institution: Clarissa Hsu, PhD Group Health Cooperative Award Amount: $1,564,384 Projected Completion Date: December 31, 2015 Description: Works with patients to design role for a clinic-community liaison to link healthcare clinics with community. Strategy aims to increase patients’ ability get what they need from both their community and their healthcare. The specific goals are to:  Create new ways to involve patients in designing their own healthcare by developing processes and tools to help patients contribute ideas for how care should be designed.  Design and test a new clinic-community liaison role for primary care teams by focusing on the prevention and treatment of chronic conditions. Featured Project Strengths:  This project follows up on an extremely promising intervention, drawing upon existing data and methodologies.  It is highly patient centered and focused on "real-world" perspective. Clarissa Hsu
  • 20. 20 Location of PCORI’s First 104 Awards 20 Total: 124
  • 22. 22 Purpose Build community Form or strengthen reciprocal relationships between researchers and non-research communities Support capacity building, co- learning, and the development of a sustainable infrastructure to facilitate ―research done differently‖ Accelerate proposal submission (or re-submission) 22
  • 23. 23 PCORI Engagement Awards – coming July 2013 Proposed by participants at October 2012 Transforming Patient-Centered Research patient engagement workshop Intended to provide resources to non–research entities for community development, capacity building, or for infrastructure development for engagement in research as partners. 23
  • 25. 25 Pre-Engagement/Community-Building Projects (Up to $15,000 for 6 months) Available to individuals, consumer/patient organizations, clinician(s) or researcher(s) or a combination of the above to support:  Community building  Creation of structure and communication strategies  Develop an understanding of PCORI, and ―research done differently‖ 25
  • 26. 26 Partnership and Infrastructure Development Projects (Up to $30,000 for 1 year) Available to emerging research/non-research partnerships to support:  Data network development  Development of infrastructure  Generation of research questions through community events, town hall meetings, etc.  Minimum 50% of funds go to non research partner(s) 26
  • 27. 27 Proposal Development Projects (Up to $50,000 for 1 year) Available to advanced research/non-research partnerships- including those who submitted PCORI proposals and were not funded - to support:  PCORI research proposal (re)submission  Research partnership skill development  Minimum 50% of funds go to non research partner(s) 27

Hinweis der Redaktion

  1. Appreciate the opportunity to visit and address you.Always forces me to stop and assess where PCORI has gotten toI find that the thinking I do in preparation gives me a new path forward for next several weeks.Just wish I could figure out how to do thinking earlier than the weekend before the talk!Several assumptions: I’m speaking to a smart and thoughtful group You’ve thought about and care about health care efficiency, getting value for the vast amounts of money we spend You won’t mind thinking with me on a set of questions.
  2. Who are the individuals responsible for carrying out PCORI’s mission?PCORI is governed by a 21-member board that represents everyone in the health care community – patients, caregivers, doctors, nurses, researchers, public health officials, payers and industry.By law, PCORI’s Board is required to include:3 members representing patients and health care consumers5 members representing physicians and providers, including at least 1 surgeon, nurse, state-licensed integrative health care practitioner, and representative of a hospital3 members representing private payers, of whom at least 1 member shall represent health insurance issuers and at least 1 member shall represent employers who self-insure employee benefits3 members representing pharmaceutical, device, and diagnostic manufacturers or developers1 member representing quality improvement or independent health service researchers2 members representing the Federal Government or the States, including at least 1 member representing a Federal health program or agencyThe directors of the National Institutes of Health and the Agency for Healthcare Research and Quality (or their designees)PCORI has established three committees: Program Development Communication, Outreach and Engagement Finance, Audit and AdministrationPCORI also has a 17-member Methodology Committee to help PCORI develop and update methodological standards and guidance for comparative clinical effectiveness and outcomes research.
  3. I want to say a few words about what we mean and why we say that we will engage, intensely and continuously. with patients and other key stakeholders in the research process. First, we want patients to help us decide what to study. This means raising the research questions and then joining with other stakeholders to prioritize those questions. We’ll fund the high priority questions. Then, after we decide what we want to fund, we invite researchers to apply. When we review their applications, there are patients and other stakeholders ON THE REVIEW PANELS.They help identify the highest quality applications, looking especially at whether the resaerch got the questions right. But beyond the review, we will have patients participating on the research teams. In fact, you don’t get funded if you don’t have relevant patients and other relevant stakeholders involved in the entireproject. Why?? Beucase we think that will increase the chances that the research is actually relevant and sticks to its purpose ofanswering patient-driven questions. And why do we do all of that?? Because we bFinally, our Advisory Panels will have….
  4. What is the purpose of the Research Agenda?The Research Agenda describes the types of research questions that can be addressed under each of the five priorities. The agenda also outlines nine criteria, taken from PCORI’s establishing legislation, which will be used to evaluate research proposals. Studies that meet most or all of these criteria will be those most likely to be funded.Why doesn’t the Research Agenda name specific conditions or treatments that PCORI is interested in funding or studying?PCORI believes there are important comparative clinical effectiveness research questions to be answered across a wide range of conditions. Focusing on a narrower set of diseases or conditions at the start of PCORI’s research funding would mean that some patients and health care issues might have no chance of benefitting from PCORI’s existence. Also, there are issues that affect patients across a variety of conditions. For example, we have heard from the patient focus groups about challenges with communication and interaction with their providers. These are problems that are not specific to one condition, but have been identified by a variety of patients as being important to them. Involving patients and other stakeholders in a meaningful process of considering which conditions or questions deserve more PCORI funding is important and will begin immediately and continue throughout PCORI’s lifetime. However, it will take time to hear all views on these issues, to weigh the input, and to begin making these choices. This must be done in a transparent manner so that all can understand how we reached the narrower, targeted set of research questions we focus on. Over time, PCORI’s research portfolio will become more focused, but PCORI will continue to reserve a portion of its funding for addressing the broader set of possible questions that patients, researchers and stakeholders may raise.
  5. Engagement: Bullet 1: collaborative relationship with the Center for Excellence in Rural Health-Hazard and HomePlace. The director and the vast majority of the staff are long-time residents of Appalachia and they have built up a firm foundation of trust and accountability with local residents. In particular, the staff at HomePlace, who are largely lay community health workers, have unparalleled success in identifying, recruiting and retaining those individuals most in need of assistance with healthcare
  6. Purpose is really two fold. To respond to the needs identified by workshop participants as well as to address PCORI’s need to accelerate funding of quality proposals and to “produce” Define community Define non research partner to include patients, caregivers, advocacy organizations, community members, clinicians and other stakeholders who will use the information generated by PCORI
  7. Workshop participants identified the need /gap for micro-contracts
  8. Design and Available Funding PCORI expects to award a total of $1.8 million dollars annually to fund projects in three different categories—Pre-engagement/Community Building Projects, Partnership and Infrastructure Development Projects, and Proposal Development Projects—that follow a logic model and progressive “framework for success” for engagement in research.
  9. Discuss the fiscal agent opportunityAwardees are expected to submit a proposal for a Partnership and Infrastructure Development Project.
  10. Awardees expected to submit a proposal for Proposal Development project