Ethics in Evaluation Research & IRB. Ethical Considerations in Research 1. Voluntary Participation 2. Informed Consent 3. Risk of Harm 4. Confidentiality.

Slides:



Advertisements
Similar presentations
Making Sense of the Social World 4th Edition
Advertisements

Informed Consent Waivers IRB Health Sciences & Behavioral Sciences University of Michigan /26/20091.
Institutional Review Board Guidance.  Independent Ethics Committee  Ethical Review Board  Research Ethics Committee 2.
 Daylene Meuschke, Ed.D Barry Gribbons, Ph.D RP Conference: April 2, 2013.
Institutional Review Board (IRB) Process Tim Noe Coordinating Center.
IRB 101: Informed Consent Columbia University Medical Center IRB September 22, 2005.
Ethics in Research. Historical Context l Past –German Experimentation –Tuskegee Syphilis Study l Present –Cancer Research –AIDS (AZT) Research.
Ethical Guidelines for Research with Human Participants
Ethics in Research.
Ethics in Research.
Ethics in Research The Ethical Standards of the American Psychological Association (2002 Ethics code, to be effective June 1,
THE ETHICAL CONDUCT OF RESEARCH Chapter 4. HISTORY OF ETHICAL PROTECTIONS The Nuremberg Code The Office for Human Research Protections (OHRP), United.
Human Subject Protection Judith Birk IRB Health / Behavioral Sciences.
Ethical Issues in Research
How to Avoid Problems in the Informed Consent Process Shannon Ontiveros, MS, CIP, CIM Institutional Review Board.
Quick Facts about Exempt Research No continuing review required IRB Reviewer makes Exempt determination 6 OHRP & 4 FDA categories(1 category overlaps)
Human Subject Research by Students at William Paterson University May 2011.
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.
The Institutional Review Board: A Community College Toolkit Dr. Geri J Anderson.
Human Subjects Research at ASU An Overview. Overview Definitions Historical Framework Federal Guidelines Human Subjects Research at ASU.
E VALUATION A SSISTANT (EA) A UGUST S ESSION STARS Alliance 2012 Tuesday Cohort C1 - Aug. 21 Wednesday Cohort C2 - Aug. 22 Noon - 1:30 pm.
R ESEARCH : A N I NTRODUCTION Compiled and Prepared by DR. BRICCIO M. MERCED, JR. Professor, Library and Information Science.
EA Project Types Formative Assessment  Looking at what works, what doesn’t, what improvements can be made to the SLC  Utilize meeting notes, experiences,
Institutional Review Board Issues for Classroom Research Sharon McWhorter IRB Administrator, The University of Akron (With assistance from Phil Allen,
RHEUMATOID ARTHRITIS PROJECT: ETHICAL REQUIREMENTS May 30, 2012.
Is IRB Review or an OHSRP Determination Required?.
Unless otherwise noted, the content of this course material is licensed under a Creative Commons 3.0 License.
What Institutional Researchers Should Know about the IRB Susan Thompson Senior Research Analyst Office of Institutional Research Presented at the Texas.
Objective 9/23/15 Today we will be completing our research methods unit & begin reviewing for the upcoming unit assessment 9/25. Agenda: -Turn in all homework.
Human Research Ethics: Issues and Procedures Dr. Constance Jones Chair, Committee for the Protection of Human Subjects.
Evaluation Assistant (EA) August Session STARS Alliance 2011 Tuesday Cohort C1 - Aug. 23 Wednesday Cohort C2 - Aug. 24 Noon - 1:30 pm.
Chapter 5 Ethical Concerns in Research. Historical Perspective on Ethics Nazi Experimentation in WWII –“medical experiments” –Nuremberg War Crime Trials.
THE TUSKEGEE SYPHILIS STUDY EFFECT ON CURRENT RESEARCH.
Session 1.05 Social and Behavioral Research Ivor Pritchard, Ph.D. Institute of Education Sciences U.S. Department of Education
Chapter 3 The Ethics and Politics of Social Research.
SoTL Research and the IRB Process Kathleen McKinney, Cross Chair in SoTL Nancy Latham, Campus IRB Executive Committee Phyllis McCluskey-Titus, SoTL Scholar.
Institutional Review Board (IRB) for Human Subjects.
The Ethics of Communication Research. Conducting Research Ethically Participation must be voluntary Participation must be voluntary Participants must.
 The purpose of IRB is to ensure the rights of research subjects are protected  In accordance with the ethical standards of the U.S. Department of Health.
Protecting Human Subjects Overview of the Issues Applications to Educational Research The IRB Process.
ETHICS & SOCIAL SCIENCE RESEARCH QUESTIONABLE PRACTICES.
GCP (GOOD CLINICAL PRACTISE)
ASH EDU 675 Week 1 Assignment Action Research Consent NEW Check this A+ tutorial guideline at
Good Clinical Practice (GCP) and Monitoring Practices
Susan Sonne, PharmD, BCPP Chair, MUSC IRB II
Class 9 Jeff Driskell, MSW, PhD
IRB BASICS Ethics and Human Subject Protections Summer 2016
Introduction to IRB (Institutional Review Board)
Jamie Reddish, MPH Research Compliance Administrator
Research with human participants at Carnegie Mellon University
Ethics in Research.
SOU Institutional Review Board
Politics/Ethics Ethics Smethics—The Laud Humphreys Approach
University of Central Florida Office of Research & Commercialization
© 2016 The McGraw-Hill Companies, Inc.
Introduction to the USC Human Subjects Protection Program
Data Ethics BPS 7e Chapter 10 © 2015 W. H. Freeman and Company.
SOU Institutional Review Board
Spaghetti & Marshmallows Experiment
Ethics lecture To publish research in psychology must first be approved be a board or committee at the institution you are working at. Institutional Review.
Basic Practice of Statistics - 3rd Edition Lecture PowerPoint Slides
Research Ethics.
What types of research are exempt and ohrp guidance on exemptions
Ethics in Evaluation Research & IRB
Online Data Collection: Ethics
Human Participants Research
SoTL Research and the IRB Process
Office of Research Integrity and Protections
Introduction to the USC Human Subjects Protection Program
Presentation transcript:

Ethics in Evaluation Research & IRB

Ethical Considerations in Research 1. Voluntary Participation 2. Informed Consent 3. Risk of Harm 4. Confidentiality 5. Anonymity

What is IRB? Institutional Review Board compliance with research ethics; government regulated for any research done Typically we think of medical studies People have the right to be informed when in an experiment The same is true in social behavioral studies People must be informed of what they are participating in and why IRB is not needed for formative evaluation

IRB: Step 1 for Research 1. Determine what you plan to study ◦ E.g. 5th graders’ attitudes about computing before your robot program and after your robot program  FYI: this is quasi-experimental, repeated measures design 2. Contact your IRB office: take the Human Subjects ethics test, fill out the IRB application 3. Begin your study AFTER obtaining IRB approval TIP- view a sample IRB application on the EA Google site :)

IRB: Step 1 for ALL Research What makes IRB complex: Obtaining consent from your participants minors require parental consent Tracking collected data accurately, consistently, over time document what you do- you will forget! Jump in and get started We’ll refine your research project throughout the semester as we discuss research design, and can amend IRB as needed