Cultural Competence Considerations [and other alliterations] in International Research IRB 2 Continuing Education March 10, 2015.

Slides:



Advertisements
Similar presentations
The Role of the IRB An Institutional Review Board (IRB) is a review committee established to help protect the rights and welfare of human research subjects.
Advertisements

1 © 2009 University of Wisconsin-Extension, Cooperative Extension, Program Development and Evaluation Human Subjects Protection (HSP)
Ethical regulations for health research involving human subjects in Cambodia By Chap Seak Chhay, MD, MPH, MHPEd Public Health and Health Professions Educator.
Fundamentals of IRB Review. Regulatory Role of the IRB Authority to approve, require modifications in (to secure approval), or disapprove all research.
Ethical Considerations when Developing Human Research Protocols A discipline “born in scandal and reared in protectionism” Carol Levine, 1988.
IRB Determinations 1. AAHRPP Site Visit Results Site visitors observed a real commitment to human subject protections Investigator and research staff.
Evaluating Risk 1 IRB CELT Presentation Colleen Donaldson – IRB Administrator Julie Wilkens – IRB Coordinator.
1 Developed by: U-MIC To start the presentation, click on this button in the lower right corner of your screen. The presentation will begin after the.
 Daylene Meuschke, Ed.D Barry Gribbons, Ph.D RP Conference: April 2, 2013.
IRB 101: Introduction to Human Subject Research
Ethical Guidelines for Research with Human Participants
© HRP Associates, Inc. Ethics & Regulation of Human Subjects Research Jeffrey M. Cohen, Ph.D., CIP President, HRP Associates, Inc.
8 Criteria for IRB Approval of Research 45 CFR (a)
Institutional Review Boards (IRB) for Indian Health Research.
THE ETHICAL CONDUCT OF RESEARCH Chapter 4. HISTORY OF ETHICAL PROTECTIONS The Nuremberg Code The Office for Human Research Protections (OHRP), United.
Scientific Data Management for the Protection of Human Subjects Robert R. Downs NASA Socioeconomic Data and Applications Center (SEDAC) Center for International.
Ethics in research involving human subjects
Who’s the Boss? Faculty Advisor or Principal Investigator Supervision versus Student Investigator or Study Coordinator Responsibilities Gwenn Snow, MS,
Cornell Evaluation Network The Use of Human Participants in Research Office of Research Integrity and Assurance ~ May 14, 2007.
International Research & Research Involving Children K. Lynn Cates, MD Assistant Chief Research & Development Officer Office of Research & Development.
1 OPHS FOUNDATIONAL STANDARD BOH Section Meeting February 11, 2011.
Human Research Protection Program Institutional Review Board Requirements and Expectations of Researchers and Research Staff Moira A Keane, MA, CIP Executive.
ORO Reviews: Frequent Findings Related to IRBs Bob Brooks Associate Director Research Compliance Education and Policy VHA Office of Research Oversight.
What makes Clinical Research Ethical? Dr Enoka Corea Co-secretary, ERC Faculty of Medicine, Colombo.
Transnational Studies IRB’s evaluation of a researcher’s plan for complying with local laws and customs when conducting transnational research.
INSTITUTIONAL REVIEW BOARD HISTORY AND ETHICS. 2 Ethical History : Holocaust : Nuremburg Trials 1964: Declaration of Helsinki :
Is Your Research Ethical? The application of Research Ethics Guidelines to Regional Health Authority Research Dr Alan Katz Need to Know: June 9, 2003.
The Role of IRBs and Ethics Susan Kornetsky, MPH Children’s Hospital, Boston.
Institutional Review Board for Human Subject Research: Does Your Research Need One? Merle Rosenzweig Michael Unsworth.
1 Protection of Vulnerable Subjects in Research Melody Lin, Ph.D. December 2012.
SUNY Oswego Human Subjects Committee Last Revised 10/28/2011.
The Institutional Review Board: A Community College Toolkit Dr. Geri J Anderson.
How to Successfully Apply to the IRB Richard Gordin, IRB Chair True Rubal, Administrator / Director For the Protection of Human Participants in Research.
IRB BASICS: Issues in Ethics and Human Subject Protections Prepared by Ed Merrill Department of Psychology November 12, 2009.
Ethical Challenge & Solution in Social Behavioral Research Melody Lin December 2012.
Institutional Review Board (IRB) What is our Purpose and Role for Ethical Research.
Human Subject Research View from the IRB Anthony J. Filipovitch Minnesota State University Mankato.
Institutional Review Board Procedures and Implications After the applied dissertation committee has approved the proposal and the IRB package, the student.
NAVIGATING THE IRB PROCESS University Institutional Review Board California State University, Stanislaus.
Carole Wells Kutztown University Andrea Chapdelaine Albright College Ana Ruiz Judy Warchal Alvernia University 11 th Annual International Association for.
AAHRPP ACCREDITATION (Association for the Accreditation of Human Protection Programs)
TUN IRB: The Basics February 26, IRB Function Review human-subject research Ensure the rights & welfare of human subjects are adequately protected.
What Institutional Researchers Should Know about the IRB Susan Thompson Senior Research Analyst Office of Institutional Research Presented at the Texas.
CUNY Human Research Protection Program (HRPP) School of Professional Studies April 18, 2013
$100 $200 $400 $500 $300 $100 $200 $400 $500 $300 $100 $200 $400 $500 $300 $100 $200 $400 $500 $300 $100 $200 $400 $500 $300 Terms Clinical Trial Facts.
APPROVAL CRITERIA AN IRB INFOSHORT MAY CFR CRITERIA FOR IRB APPROVAL OF RESEARCH In order for an IRB to approve a research study, all.
WELCOME to the TULANE UNIVERSITY HUMAN RESEARCH PROTECTION OFFICE WORKSHOP for SOCIAL/BEHAVIORAL RESEARCH (March 2, 2010) Tulane University HRPO Uptown.
ETHICAL ISSUES AND INFORMED CONSENT Juan M. Lozano, MD, MSc Department of Paediatrics and Clinical Epidemiology Unit School of Medicine, Javeriana University.
M6728 Ethics in Research Informed Consent/IRBs Reporting Research Results.
Chapter 5 Ethical Concerns in Research. Historical Perspective on Ethics Nazi Experimentation in WWII –“medical experiments” –Nuremberg War Crime Trials.
Medical Research in Times of Bioterrorism - OHRP’s Perspective Michael A. Carome, M.D. Associate Director for Regulatory Affairs Office for Human Research.
 What is an IRB and why do we need one at Western?  Who needs to submit proposals to the IRB?  If approved, how long is your proposal good for?  Is.
Chapter 2: Ethical Issues in Program Evaluation. Institutional Review Boards (IRBs) Federal mandate for IRBs –Concern during 1970s about unethical research.
Doing IRB Right … Together JOHN POTTER, OD, MA Chair, Institutional Review Board.
1 Usability Analysis n Why Analyze n Types of Usability Analysis n Human Subjects Research n Project 3: Heuristic Evaluation.
Investigator Initiated Research Best Practices for IRB: SBER Corey Zolondek, Ph.D. IRB Operations Manager Wayne State University.
Christine Yalda, J.D., Ph.D. Chair, Human Research Review Committee Grand Valley State University.
Scientific and Scholarly Validity
Back to Basics – Approval Criteria
© 2010 Jones and Bartlett Publishers, LLC
Investigator Responsibilities in Human Subjects Research
Jeffrey M. Cohen, Ph.D. CIP President HRP Associates, Inc.
Dr Veena Pillai Dhi Consulting & Training
Research Ethics Matthew Billington
© 2016 The McGraw-Hill Companies, Inc.
Greg Nezat CRNA, PhD CDR/NC/USN Chairman, IRB II
CUNY Human Research Protection Program (HRPP)
Ethics in Practice: Guidelines and Regulations
Office of Research Integrity and Protections
Research with Human Subjects
Presentation transcript:

Cultural Competence Considerations [and other alliterations] in International Research IRB 2 Continuing Education March 10, 2015

Outcomes Consider utility of cultural competence frameworks in the assessment of graduate student’s international research Address the IRB’s purview in assessing risk related to socio-cultural and political contexts in international research If there’s time, further distinguish the larger scope and role of the IRB in the evaluation of international research

Intercultural Knowledge & Competence AACU Intercultural Knowledge & Competence Value Rubric: Knowledge:Cultural Self-Awareness Knowledge:Knowledge of Cultural Worldview Frameworks Skills: Empathy Skills: Verbal and Nonverbal Communication Attitudes: Curiosity Attitudes: Openness

What is International Research Research studies are considered to have an international component when investigators travel abroad to collect data or investigators use or collect data from participants who are outside of the U.S. Examples include: 1.A researcher traveling to Brazil to conduct a survey with a Brazilian population 2.A researcher analyzing identifiable biological specimens that were collected in India 3.Researchers in the United States conducting an online survey in which subjects who live in other countries may respond.

International Research & Federal Regulations Federal regulations for oversight of international research, together with the Association for Accreditation of Human Research Protection Programs (AAHRPP) make the following stipulations: – The researcher must provide the same or equivalent protections to human subjects in research conducted in other countries. The protections need not be identical to those provided in the U.S. but must be equal in function or effect. Subject autonomy and dignity should be respected. Protections should encompass the ethical principles of respect for person, beneficence, and justice.

International Research & Federal Regulations Federal regulations for oversight of international research, together with the Association for Accreditation of Human Research Protection Programs (AAHRPP) make the following stipulations: – The researcher must be familiar with and comply with local laws, regulations, political and socio-economic factors, and cultural context in all locations where the research is conducted. – The researcher must have sufficient knowledge of the local context, which may impact all aspects of the research design, and in particular, the protection of the rights and welfare of subjects.

Local Context Seattle University IRB: “The level of knowledge about the local context and local law required for approval is based on the degree of risk to potential research participants. Higher risk studies require more thorough considerations of local context and inclusion of strategies to mitigate harm than do minimal risk studies. In such cases, the IRB may request consultation with experts in the particular international setting.”

Local Context OSU IRB Asserts that relevant local context information should be included in the IRB protocol. This includes, but it not limited to, the following: – A description of the research team’s knowledge of or experience in the host country as well as any relevant qualifications for conducting the proposed research within the international setting should be included in the Investigator Qualifications and/or Training and Oversight sections of the IRB protocol. – Cities, regions countries where research will be conducted – Scientific/ethical justification for conducting the research in an international setting – Economic status of the country/community – Current events or socio-political environment in the country that may impact research conduct or alter the risks or benefits to subjects – Societal and cultural beliefs in the country that may impact research conduct or alter the risks or benefits to subjects – If women and children are part of the subject population, their role in the society, including their autonomy and legal capacity to make decisions.

Local Context OSU IRB Asserts that relevant local context information should be included in the IRB protocol. This includes, but it not limited to, the following: – If there are circumstances in which women or community members do not have the autonomy to make decisions for themselves, the plan for obtaining informed consent from both the study subject and any additional authority figures should be included in the Consent Process section of the IRB protocol. – Literacy rate of the potential subject population – Languages and dialects of the potential subject population – Involvement of organizations, community leaders, or experts in engaging the subject population or conducting the research – Relevance of the research to the area’s health, economic, educational, or other needs – Distribution of risks and current and future benefits (Tufts University, 2014). – A description of how the plan for recruitment and subject selection will avoid undue influence or favoritism within the subject population.

Considerations: Research Methods What recruitment methods will be used? – Do those methods violate cultural norms of confidentiality? Does the collection data or specimens involve sensitive, identifiable information? How experienced is the PI in doing research in that country? Panageas, H. & Diccianni, K. (2009). IRB refresher 2009: International research. Presented at the NYU School of Medicine Institutional Review Board Meeting, New York City, NY.

Considerations: Informed Consent Are there important historical or cultural considerations? Who will be doing the actual consent process? Consent documentation: – Translation – not just words, but culturally-appropriate concepts e.g., explaining randomization in terms of a lottery – Is a written form appropriate? – Signature requirements Panageas, H. & Diccianni, K. (2009). IRB refresher 2009: International research. Presented at the NYU School of Medicine Institutional Review Board Meeting, New York City, NY.

Discussion In what ways can the OSU IRB obtain knowledge of local research context? Panageas, H. & Diccianni, K. (2009). IRB refresher 2009: International research. Presented at the NYU School of Medicine Institutional Review Board Meeting, New York City, NY.

Discussion In what ways can the OSU IRB obtain knowledge of local research context? – Consultant Interface or Consultant Documentation: United States Faculty International Faculty International IRB member Other Networks – Knowledgeable IRB Member or Administrator – Site Visits Panageas, H. & Diccianni, K. (2009). IRB refresher 2009: International research. Presented at the NYU School of Medicine Institutional Review Board Meeting, New York City, NY.

Discussion When investigators are indigenous to the international research site, does that origination sufficiently qualify them or does the IRB need additional consultation?

Discussion If the research plan is not culturally sensitive or appropriate but the research poses no risk, does the IRB require changes to ensure that the subjects are not insulted or irritated?

Discussion What is the IRB’s purview, if any, regarding the cultural competence of graduate student investigators?