Human Studies Program Office of Research Compliance Vice Chancellor for Research and Graduate Education CTE DCS IRB Series – Event 3 December 1,2014 Denise.

Slides:



Advertisements
Similar presentations
IRB SUBMISSION PROCESS FOR SHB STUDIES Version 9/18/2013.
Advertisements

Digital Assets Presented by Sharon Rivenson Mark, Esq. and Shirley B. Whitenack, Esq. Adapted from Presentation by Catherine A. Seal, Esq.
1 The HIPAA Privacy Rule and Research This presentation will probably involve audience discussion, which will create action items. Use PowerPoint to keep.
HIPAA – Privacy Rule and Research USCRF Research Educational Series March 19, 2003.
Informed Consent.
Research Involving Human Subjects All research involving the participation of human subjects must be submitted for review by the IRB (Institutional Review.
© HRP Associates, Inc. Informed Consent, Parental Permission & Assent Jeffrey M. Cohen, Ph.D., CIP President, HRP Associates, Inc.
Human Studies Program Office of Research Compliance Vice Chancellor for Research and Graduate Education Denise Lin-DeShetler, M.P.H., M.A. Director, Human.
1 Laura Odwazny Senior Attorney Office of the General Counsel U.S. Department of Health and Human Services Research Using Data Mined from the Internet.
CIPA Update. FOR SCHOOLS – By July 1, 2012, amend your existing Internet safety policy (if you have not already done so) to provide for the education.
Evaluating Risk 1 IRB CELT Presentation Colleen Donaldson – IRB Administrator Julie Wilkens – IRB Coordinator.
Exempt Research Mary Banks BS, BSN IRB Director CRC IRB and BUMC IRB.
Riverside Community School District
Protecting Human Participants in Research syr
IRB 101: Informed Consent Columbia University Medical Center IRB September 22, 2005.
Cooperative Research IRB Brownbag, 3/4/08. ISU Policy Cooperative research projects are those projects which involve more than one institution. The official.
CUMC IRB Investigator Meeting November 9, 2004 Research Use of Stored Data and Tissues.
8 Criteria for IRB Approval of Research 45 CFR (a)
Informed Consent and HIPAA Tim Noe Coordinating Center.
IRB Monthly Investigator Meeting Columbia University Medical Center IRB October 11, 2005.
FAMILY EDUCATIONAL RIGHTS AND PRIVACY ACT Electronic Signatures This work is the intellectual property of the author. Permission is granted for this material.
Human Investigation Committee  Is it research?  If yes, does it involve human subjects?  If yes, can it be exempt?  If no, will a Request for.
Quiz 2 - Review. Identity Theft and Fraud Identity theft and fraud are: – Characterized by criminal use of the victim's personal information such as a.
Is this Research? Exempt? Expedited?
Copyright ©: SAMSUNG & Samsung Hope for Youth. All rights reserved Tutorials The internet: Social networks and communities Suitable for: Improver.
How to Obtain Institutional Review Board (IRB) Approval Richard Wagner Associate Director UCSF Human Research Protection Program August 14, 2008.
Cornell Evaluation Network The Use of Human Participants in Research Office of Research Integrity and Assurance ~ May 14, 2007.
Avoiding the Pitfalls of an IRB Submission Chris Ayres Chair, Institutional Review Board Social & Behavioral Science & Chair, Department of Kinesiology,
International Research & Research Involving Children K. Lynn Cates, MD Assistant Chief Research & Development Officer Office of Research & Development.
Using the Internet to Conduct Research What Investigators and IRB Members Should Know -- January 29, Lisa Shickle, MS Analyst, VCU Massey Cancer.
HRPP Training – Session Two Human Research Protection Program Manager
What is your Acronym IQ? ASC DOC DOS FYS SACS NEH NIH OSHA IRB TGIF.
Help us Help you: IRB Policy Updates Susan Bankowski, MS, JD IRB Chair.
IRB Board Education Session 6 How Consent Regulations are Implemented in INSPIR Mary Banks Director, Office of the IRB June -July 2005.
Teaching Research Methods (Classroom Protocols) Boston University Charles River Campus Boston University Medical Center Mary A. Banks BS, BSN IRB Director.
1 Ethics of Working with Human Subjects (BIOL/CHEM 397 ) Header image designed by Michelle Jordan, UMBC Creative Services, 2009.
RESPONSIBLE CONDUCT IN HUMAN SUBJECTS RESEARCH MARGARITA M. CARDONA DIRECTOR OF SPONSORED RESEARCH Institutional Review Board.
Privacy and Confidentiality. Definitions n Privacy - having control over the extent, timing, and circumstances of sharing oneself (physically, behaviorally,
Office of Research Integrity and Compliance March 2011.
HUMAN SUBJECTS PROTECTION PROGRAM Office Location: 1350 N. Vine Ave. (one block west of Cherry Ave. & three blocks north of Speedway) PO Box Phone:
Privacy vs. Confidentiality.  IRB review of privacy and confidentiality protections is required under the Common Rule and the FDA regulations, as well.
Institutional Review Board Procedures and Implications After the applied dissertation committee has approved the proposal and the IRB package, the student.
Marian University is sponsored by the Sisters of St. Francis, Oldenburg. Human Subjects Research and the Marian University Institutional Review Board (IRB)
Education Research and Social & Behavioral Science IRB.
Institutional Review Board Issues for Classroom Research Sharon McWhorter IRB Administrator, The University of Akron (With assistance from Phil Allen,
Virtual Business Virtual Communication Copyright © Texas Education Agency, All rights reserved.
CUNY Human Research Protection Program (HRPP) School of Professional Studies April 18, 2013
Case Studies: Puzzles in Human Research Kevin L. Nellis, M.S., M.T. (A.S.C.P.) Program Analyst, Program for Research Integrity Development and Education.
Privacy & Confidentiality in Internet Research Jeffrey M. Cohen, Ph.D. Associate Dean, Responsible Conduct of Research Weill Medical College of Cornell.
SACHRP Recommendations on Internet Research Edward E. Bartlett, PhD Office for Human Research Protections October 7, 2015.
 Empowered by the University to insure we are in compliance with Federal regulations  Guided by the standards in the Belmont Report and regulations.
Social Media, Internet-based Research, and Ethics: Challenges and Strategies Stanley Estime, MSCI, CIP Senior QA/QI Specialist Tel:
Protecting Human Subjects Overview of the Issues Applications to Educational Research The IRB Process.
Informed Consent Presented by Marian Serge, RN. Goals Informed consent process and form Title 38 CFR , Common Rule required elements and additional.
Certificates of Confidentiality:
Investigator of Record – Definition
© 2016 The McGraw-Hill Companies, Inc.
Common Rule Changes to Consent and Template
The HIPAA Privacy Rule and Research
This takes approximately 5 minutes or less from start to finish
Investigator of Record – Definition
Practical Guidance on the Use of Social Media for Recruitment
Jeffrey M. Cohen, Ph.D. Associate Dean,
Informed Consent (SBER)
Common Rule Update: Exempt categories UT IRB
What are the Major Changes to the IRB under the Final Common Rule?
IRB Educational Session - IRB Regulations on Expedited Review
Office of Research Integrity and Protections
Research with Human Subjects
Office of the Vice President for Research Human Subjects Protection Program IRB Submission Process Module 4 - Health Insurance Portability and Accountability.
Presentation transcript:

Human Studies Program Office of Research Compliance Vice Chancellor for Research and Graduate Education CTE DCS IRB Series – Event 3 December 1,2014 Denise Lin-DeShetler

Human Studies Program Office of Research Compliance  Why do we need to discuss internet research? ◦ Research about internet and using internet is increasingly popular and important ◦ Federal regulations were written before internet became universal  They are currently silent about the use of internet for research involving human participants  Some guidance available, but they are ever-evolving; based on FAQs

Human Studies Program Office of Research Compliance “Internet Research” as a tool for research and as a locale or venue of research: ◦ Research involving study of information already available on the Internet ◦ Using Internet as a medium for recruiting or interacting with subjects ◦ Research about the Internet itself and its effects (e.g., popularity of social media types) ◦ Research about Internet users ◦ Internet used as an experimental intervention

As a tool…As a locale…. Research involving:  Survey instruments, databases, search engines, databanks  May not involve direct interaction with human participants, but PII may still be collected Research (qualitative and quantitative) that utilizes Internet “spaces” such as: Chat rooms, gaming world, other other simulated locales But…. Research methods using Internet phoning, video conferencing or online chat (i.e., Facetime, Skype) can be both use as a tool and a locale.

Human Studies Program Office of Research Compliance Stages in a Research Project 1. Recruitment 2. Data Collection As a tool…. Observations Data Mining 3. Publication of Results Possible re-recruitment

Human Studies Program Office of Research Compliance Advertising Consent Process Enrolling Participants

Human Studies Program Office of Research Compliance  The recruitment material placed on the internet should follow similar rules of any other recruitment material: ◦ Are not unduly coercive ◦ Do not promise or imply favorable outcomes or other benefits apart from what is written in the protocol ◦ Do not communicate that the study product (or intervention) is safe or effective for the purposes under investigation ◦ Do not make claims that the product or intervention is known to be equivalent or better to any other product or intervention ◦ Do not use language that regulatory authorities, such as the IRB, have approved the research ◦ Do not emphasize payment

IRB Should Review IRB Do Not Need to Review  Paid advertisements  In-text advertisements  Advertisements on social networks  Social network page to promote study  Any study-specific direct advertisements via blog, blog post, tweet, or text  Advertisement of study- specific information limited to basic trial information (title, purpose, and study locations)  Communication that are education or provide generation information (i.e., podcast describing symptoms of HIV)  Study-specific publicity intended for general audience (i.e., news stories )

Human Studies Program Office of Research Compliance  Types of internet-based recruitment methods: ◦ ◦ Online Advertising ◦ Chatroom Postings  All recruitment materials need to be reviewed and approved before use.  General listings of research studies on websites that provides limited information do not need prior approval from IRB (e.g., SONA, Clinicaltrials.gov) 1.Study Title 2.Purpose 3.Protocol Summary 4.Contact information

Human Studies Program Office of Research Compliance  Sending promotional messages (ads) about a study without using the medium in ways typical of a common user. ◦ Is this appropriate use of the website? ◦ Intrusive to potential participants?  Advertising in social network sites or Twitter groups, such as a cancer support group, may seem intrusive and inappropriate to members of that group

Human Studies Program Office of Research Compliance Appropriate methods for documenting consent should reflect the risk and complexity of the research ◦ For minimal risk: waiver of consent whereby participants click on the “I agree” statement on consent form to proceed to research activities  Must meet the regulatory criteria for a waiver of informed consent ◦ For more than minimal risk:  Traditional signed consent, returned to PI who will then give consenting participants password to access research material  E-signatures  Consent process through chat, , or other online venue

Human Studies Program Office of Research Compliance  Child participants: ◦ Authentication of age with use of age verification systems ◦ When research involves participation of minors, both child assent and parental consent still applies, unless research meets appropriate criteria for waiver of parental permission  Readability ◦ It is more difficult for investigators to discern whether or not their participants understand the consent because process can be done asynchronous, and the opportunity to ask the researcher questions about the research is usually slim.

Human Studies Program Office of Research Compliance  When obtaining consent over the internet, we assume that potential participants at least 18 years old ◦ Age verification systems ◦ Questions that are more easily answerable to one who is at least 18 (i.e., identifying images of old items)  To authenticate identity when research involves more than one interaction: ◦ Provide study participants PIN to be used for subsequent computer and internet-based data collection.

Human Studies Program Office of Research Compliance Public vs. Private Domains

Human Studies Program Office of Research Compliance Data Mining Informational Risks

Human Studies Program Office of Research Compliance Case 2: A researcher wants to collect data from an HIV support group website on Facebook to examine how much perceived support participants are receiving from participating in different types of support (chat groups vs. support group sessions vs. blogs) they learn from subscribing to the website. The website allows users to make suggestions about the usability of the different resources the website provides. Does this study require IRB approval if no names or other identifiers are collected? Can this study be done without PII?

Human Studies Program Office of Research Compliance Per 45 CFR (b), research using only secondary data that is publicly available or de-identified do not need IRB approval However: Research that utilizes data from blogs, newspaper responses, and social media networks should not have the same rules for IRB approval because the expectations of privacy by participants varies depending on the venue

Human Studies Program Office of Research Compliance Is there unauthorized disclosure of illegal behavior, substance abuse, or chronic illness?  Legality/ Criminal acts  Stigmatization  Financial  Reputation We look at identifiable information that is being collected:  User posting on study-specific website in which user may be sharing PII  De-identified quotes gathered from blogs that can inadvertently be traced back to individual  Repurposed photograph of individuals or group posted on website without permission

Human Studies Program Office of Research Compliance  Publicly available means: ◦ Available at no charge to anybody with a computer ◦ Available to anybody willing to pay the requisite fee ◦ Available to anybody who meets the terms of a use agreement  Data that is publicly available qualifies for exemption

Human Studies Program Office of Research Compliance  Privacy: refers to individuals’ right to have control over access to themselves and their information  Confidentiality: refers to how information that is obtained from individuals is protected.

Human Studies Program Office of Research Compliance Private information (in research) is “information about behavior that occurs in a context in which an individual can reasonably expect that no observation or recording is taking place, and information which has been provided for specific purposes by an individual and which the individual can reasonable expect will not be made public (e.g., medical records).  If the individual intentionally posts information on the internet, then this is public information, UNLESS the policies and/or terms of service of the entity hosting the information indicates this is “private.”  Some may assume their post is “private” but are in fact, not.  If in doubt, always go conservative. That is, consider it private information.