Phase 1 Preliminary Results – Survey of Publicly Available Research Ethics Resources at State and Territorial Departments of Health Michelle Conklin, B.S.

Slides:



Advertisements
Similar presentations
Managing Compliance Related to Human Subjects Research Review Joseph Sherwin, Ph.D. Office of Regulatory Affairs University of Pennsylvania Fourth Annual.
Advertisements

Western Balkan Countries INCO.NET WP 4 - Building Capacities Nikos Sidiropoulos, General Secretariat of Research And Technology (GSRT), Ministry of Development,
Yvonne Lau, MD, PhD, MBHL NIH Extramural Research Integrity Officer OD/OER/OEP National Institutes of Health OER Regional, June 2013.
Arkansas MSP Grants: Statewide Evaluation Plan Judy Trowell Arkansas Department of Education Charles Stegman Calli Holaway-Johnson University of Arkansas.
Measuring Ethical Goals of Research Oversight Holly Taylor, PhD, MPH Department of Health Policy and Management Bloomberg School of Public Health Berman.
Multisite Human Subjects Research CUNY HRPP Coordinator Training October 19, 2012.
Recently Issued OHRP Documents: Guidance on Subject Withdrawal and Draft Revised FWA Secretary’s Advisory Committee on Human Research Protections October.
1 Involvement of Non-VCU Institutions in VCU Human Subjects Research Prepared for the 5 th Thursday for Human Subjects Protection Program 3/07.
OREGON PUBLIC HEALTH DIVISION Office of Environmental Public Health Radiation Emergency Preparedness and Response Capabilities in State Health Departments.
Introduction & Background Laurene Christensen National Center on Educational Outcomes National Center on Educational Outcomes (NCEO)
Institutional Review Boards (IRB) for Indian Health Research.
Human Subjects Research Dr. John S. Irvine Chairperson, NMSU Institutional Review Board for Human Subjects Research
IRB-Investigator/ Research Coordinator Mtg. Conducting Research at Non-Columbia Sites Including International Research September 14, 2004 George Gasparis.
CUMC IRB Investigator Meeting IRB Frequently Asked Questions October 11, 2005.
Ethical Issues in Research
Be a Public Health Nurse
Federalwide Assurance Presentation for IRB Members.
Lisa Denney, MPH HRPP Assistant Director Melanie Mace, MA HRPP Education and Training Coordinator Bill Woods, PhD CAPS Policy and Ethics Core November.
NLM Database Central: The First Place to Look for Your PHSR Research Data F. Douglas Scutchfield 1, M.D., Michelyn W. Bhandari 2, DrPH, and Allison Amrhein,
Responsible Conduct of Research (RCR) Farida Lada October 16, 2013
FRAMING THE DISCUSSION MAY 16, 2014 Protecting People through Tribal Public Health Codes: Legal Technical Assistance and Resources for Tribes and Tribal.
Institutional Research Compliance Juliann Tenney, JD Research Compliance and Privacy Officer Director, Institutional Research Compliance Program.
DrugEpi 1-4 Counting HS Marijuana Use Module 1 Overview Context Content Area: Descriptive Epidemiology & Surveillance Essential Question (Generic): How.
Help us Help you: IRB Policy Updates Susan Bankowski, MS, JD IRB Chair.
ORAL HISTORIES AND HUMAN SUBJECTS RESEARCH PROTECTION REQUIREMENTS April 18, 2012.
Responsible Conduct of Research (RCR) What is RCR? New Requirements for RCR Who Does it Affect? When? Data Management What is the Institutional Plan? What.
Office of Sponsored Programs All rights reserved GTRC Finding Funding.
How Did Information Technology Boost the Dissemination of Community-wide Antibiogram to Healthcare Providers? Lei Chen, PhD, Sr. Epidemiologist Steve B.
1 General Structure of a System Dealing with Research Misconduct - General Remarks on its diversity - Makoto Misono National Institute of Technology and.
CCAS Annual Conference: New Orleans, LA November 11, 2010 The Role of Deans: Regulatory & Administrative Responsibilities Michelle Feige, MSW Public Health.
Institutional Review Board Procedures and Implications After the applied dissertation committee has approved the proposal and the IRB package, the student.
11/12/20151 IRBs from Both Sides Now Bennett I. Bertenthal Indiana University.
Environmental Health Specialist Network: Drinking Water Program By: Joyce Tuttle, REHS, PHM.
Yadvindera (Bobby) Bains MD Director of Radiation Oncology, Laredo Medical Center Adjunct Associate Professor, Dept of Radiation Oncology, University of.
AAHRPP ACCREDITATION (Association for the Accreditation of Human Protection Programs)
SACHRP PANEL: HOLDING EXTERNAL IRBS ACCOUNTABLE David L. Wynes, Ph.D. Vice President for Research Administration Emory University July 21, 2009.
Post-Approval Monitoring (PAM) Program November 17, 2015.
BioSense 2.0  BioSense is a nationwide collaborative system for protecting and improving population health by providing timely information for better.
Paul Kelly Facility Research Compliance Officer for the Ralph H. Johnson VA Medical Center.
Brian Smith Associate Vice Chancellor, Research Infrastructure and Operations Academic Senate Committee on Research December 15, 2014.
 Successful surveillance includes appropriate partnerships, sampling, IRB authorizations and an effective system for documentation.  Once a surveillance.
 The development of the perinatal assessment tool was a vital precursor leading to the addition of data collection of the perinatal population. Data collected.
Institutional Review Board Procedures and Implications After the applied dissertation committee has approved the proposal and the IRB package, the student.
Introduction to the HRPP and IRB Human Research Protection Program (HRPP) Office.
Does My Project Require HRPP/IRB Review? Research Human Subject Engagement HUMAN RESEARCH PROTECTION PROGRAM (HRPP) OFFICE.
 Federal Governmental Agencies  National Nursing Organizations  Specialty Nursing Organizations  Private Foundations.
Increased # of AI/AN receiving in- home environmental assessment and trigger reduction education and asthma self-management education Increased # of tribal.
| Contact CDC at: CDC-INFO or The findings and conclusions in this report are those of the authors and do not necessarily.
Chapter 4: Nursing Resources for Epidemiology. Introduction Data collection and analysis is a core area of epidemiology. Epidemiologists gather data from.
Lisa Hoebelheinrich, JD, CHRC Associate Vice Chancellor, Compliance
The Essentia Institute of Rural Health (EIRH) is
Patricia M. Alt, Ph.D. Dept. of Health Science Towson University
Public Health Practice vs Research: Implications for Preparedness and Disaster Research Review by State Health Department IRBs David Perlman, Ph.D. Former.
Overview: IRBshare  IRBchoice
Faculty Orientation- Research
Brown Bag Series First Tuesday of each month (except July)
AAHRPP Accreditation Welcome to the University of Georgia’s presentation for accreditation of the human research protection program (HRPP). This presentation.
Sponsored Programs at Penn
Multisite Human Subjects Research
Human Subjects Office & Institutional Review Board
Does My Project Require HRPP/IRB Review?
Learn the Signs. Act Early.
2/1/2019 3:33 PM Tennessee State University Institutional Review Board
GSBM Presentation Updated
Exploring 45 CFR , Criteria for IRB Approval of Research
National Institutes of Health, USA Office of Extramural Research
Everything You Wanted to Know about UOPX IRB
GPS IRB SIX STEPS Updated
IRB Harmonization 2016 Review
IRB submissions for researchers
Presentation transcript:

Phase 1 Preliminary Results – Survey of Publicly Available Research Ethics Resources at State and Territorial Departments of Health Michelle Conklin, B.S. 1 Jenna Mullet 1 David Perlman, Ph.D. 1,2 1 University of Pennsylvania 2 University of the Sciences, Philadelphia

What is Project Phobos? Phobos is one of the moons of Mars. But it also stands for: – Public health (the Ph) – Behavioral (the B) – Social (the S) Project Phobos will concentrate on research on these three areas of science and health.

Phases of Project Phobos PhaseDescriptionType of Project 1A preliminary analysis of publicly available information about the research ethics infrastructure and processes at State Departments of Health (DOHs). Research 2A survey of DOHs regarding their knowledge, use, and dissemination of guidance documents and processes for distinguishing public health practice from research. Research 3Educational and decision tools to be produced by Dr. Perlman's small business, E4 - Eclipse Ethics Education Enterprises, LLC and hopefully funded by small business grants and contracts from appropriate federal agencies. Research and Development 4A national, independent Institutional Review Board (IRB) for public health research and a human research protection program (HRPP) that will assist agencies and DOHs in properly distinguishing public health research and practice. Research and Development

Introduction Parsing public health activities into human subjects research (which requires Institutional Review Board (IRB) oversight) and practice (which does not) can be vexing (Perlman, 2008).

Guidance Can Help The Center for Disease Control (CDC) and the Council of State and Territorial Epidemiologists (CSTE) have guidance to help.

Much Is Unknown Much is unknown about how states and territories distinguish research from practice, including: 1.who makes the determination; 2.the extent of awareness and use of CDC and CSTE guidance; and 3.what infrastructure, policies, and procedures exist.

Methods Using public information, we determined how many states and territories operate an IRB and have federalwide assurances (FWAs). We also searched state and territory Departments of Health websites for mention of research versus practice information.

Findings StateTerritories IRBs391 Active FWA443 Inactive FWA50 Website mentions CSTE Report 40 Website mentions CDC Guidance 10 Website mentions both CSTE and CDC 40 Website mentions other information 130

Conclusions This data might indicate lack of awareness of this public health issue. This preliminary analysis helps to answer some of our research questions; however, conducting quantitative and qualitative surveys will help confirm these preliminary results and provide more detail.

Data Available Online Our results and data are publicly available at

Questions and Contact Information David Perlman, Ph.D. Visiting Professor, University of the Sciences, Philadelphia Senior Lecturer, Penn Nursing Associate, Penn Center for Bioethics Interested in collaborations and ideas on funding Phase 2 of this project