Science Fair Research Plan

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

Ethics in Field Research Philip Verwimp 27 February, 2014.
Annual IRB Member Training October 2010 Research Participant Compensation John Stillman Director Institutional Review Board University of Utah.
TODAY’S TOPIC: Ethics – deconstructing consent and participation with “vulnerable” populations.
Chapter Four. Writing the Proposal  What does the intended reader/audience need to understand better about the topic?  What does the audience know little.
PPA 501 – Research Methods in Administration Lecture 2b - Ethics.
Ethical Guidelines for Research with Human Participants
PSYCO 105: Individual and Social Behaviour Lecture 1: The Ways and Means of Psychology.
Ethics People should be treated as ends not means.
8 Criteria for IRB Approval of Research 45 CFR (a)
Chapter 3 Preparing and Evaluating a Research Plan Gay and Airasian
FOUNDATIONS OF NURSING RESEARCH Sixth Edition CHAPTER Copyright ©2012 by Pearson Education, Inc. All rights reserved. Foundations of Nursing Research,
1 Psychology 2020 Unit 1 cont’d Ethics. 2 Evolution of ethics Historic Studies Tuskegee Syphilis Study ( ) Milgram’s Obedience Study (1960s)
How to Obtain Institutional Review Board (IRB) Approval Richard Wagner Associate Director UCSF Human Research Protection Program August 14, 2008.
Psychology 291 – Lab 4 Ethics October 9, 2012
Using the Internet to Conduct Research What Investigators and IRB Members Should Know -- January 29, Lisa Shickle, MS Analyst, VCU Massey Cancer.
Human Research Ethics and Obtaining Ethics Approval
Research Involving Human Subjects All research involving the participation of human subjects must be submitted for review by the IRB (Institutional Review.
University of Western Sydney Comments on your HREC Application.
DrugEpi 1-4 Counting HS Marijuana Use Module 1 Overview Context Content Area: Descriptive Epidemiology & Surveillance Essential Question (Generic): How.
Institutional Review Board (IRB) Human Subject Dr. John N. Austin, Director and Ms. Renee S. Jones, Associate Director Delaware State University Office.
Research Involving Human Subjects All research involving the participation of human subjects must be submitted for review by the IRB (Institutional Review.
Regulatory criteria for approval Bob Craig, July 2007.
The IRB Approval Process Michael Bingham, JD Assistant Director, University of Wisconsin-Madison Education IRB
Brief Introduction to Review of Human Subjects Research in the Health Sciences Presentation to Primary Care Faculty Development Program Nichelle Cobb,
Writing a Successful IRB Application Karen Adams Regulatory Specialist, ITHS May 17, 2013.
IRB Belmont Report Federally mandated Risks -> minimized & reasonable Informed consent rospective Approval Prospective Approval Monitoring for subject.
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.
Institutional Review Board (IRB) What is our Purpose and Role for Ethical Research.
SUNY Oswego Human Subjects Committee Last Revised 10/28/2011.
Classroom Project CAGS Workshop Alaska, Research/Education Needs to address –AIM, –CloudSat, –GLOBE –Education Standards –Your curriculum.
Writing Research Proposal ADS501 Research Method and Data Analysis.
Marian University is sponsored by the Sisters of St. Francis, Oldenburg. Human Subjects Research and the Marian University Institutional Review Board (IRB)
NAVIGATING THE IRB PROCESS University Institutional Review Board California State University, Stanislaus.
SCIENCE FAIR The Sweet Sound Of Science Fair Paperwork Rustling On My Desk! Link to Science Fair Paperwork Forms.
Science Fair Background Research Paper
Experimenting on Animals Harold Herzog – two arguments used by animal rights activists The utilitarian argument – equality Peter Singer - the capability.
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.
APPROVAL CRITERIA AN IRB INFOSHORT MAY CFR CRITERIA FOR IRB APPROVAL OF RESEARCH In order for an IRB to approve a research study, all.
Donna B. Konradi, DNS, RN, CNE GERO 586 Understanding the Ethics of Research.
Setting up Logbooks Working like a Scientist Bound All entries written in blue or black pen. If mistakes are made, strikethrough, initial and write correction.
Chapter 1 These notes are to be written in your composition book.
Chapter 5 Ethical Concerns in Research. Historical Perspective on Ethics Nazi Experimentation in WWII –“medical experiments” –Nuremberg War Crime Trials.
INTERNATIONAL SCIENCE AND ENGINEERING FAIR Rules and Guidelines 2016.
The Core of IRB Review William L. Freeman, MD, MPH, CIP [with material by Jeff Cohen & Moira Keane] FALCON Meeting, Las Vegas, NV December 6, 2008 Director.
 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.
 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.
Getting Started: Do’s and Don’ts Adapted from Indian River County Science Fair Website.
Investigator Initiated Research Best Practices for IRB: SBER Corey Zolondek, Ph.D. IRB Operations Manager Wayne State University.
Research Plan The Research Plan/Project Summary should include the following: a. RATIONALE: Include a brief synopsis of the background that supports your.
9 Procedure for Conducting an Experiment.
IRB Example Forms and Research Paperwork
Back to Basics – Approval Criteria
Chapter 3: Ethical guidelines for psychological research.
I’ve Chosen a Project… Now What?!
Broward County Regional Science and Engineering Fair (BCRSEF)
1. Must fill in all information on page 1 and 2 for individual projects. 2. Team projects must fill out pages Dates will be whenever you.
Jeffrey M. Cohen, Ph.D. CIP President HRP Associates, Inc.
ST3004: Research Methods Ethics and Writing your Proposal
© 2016 The McGraw-Hill Companies, Inc.
ETHICAL CONSIDERATIONS IN THE CONDUCT OF HEALTH SCIENCES RESEARCH
Link to Science Fair Paperwork Forms
Onslow County Schools Science Fair and Engineering Fair
Intro to Projects – Research with Human Subjects
Greg Nezat CRNA, PhD CDR/NC/USN Chairman, IRB II
The Need for Ethical Principles
BWHS Science Research Project Guidelines for
Presentation transcript:

Science Fair Research Plan How do I complete my research plan for my science fair project?

Research Plan The Research Plan/Project Summary is a succinct detailing of the rationale, research question(s), methodology, and risk assessment of your research project and should be completed before the start of your experimentation. Any changes you make to your project should be added to the final document.

What should my research plan have? The research plan for ALL projects should include the following: a. What is the RATIONALE for your project? Include a brief synopsis of the background that supports your research problem and explain why this research is important scientifically and if applicable, explain any societal impact of your research. b. State your HYPOTHESIS(ES), RESEARCH QUESTION(S), ENGINEERING GOAL(S), EXPECTED OUTCOMES. How is this based on the rationale described above?

What should my research plan have? c. Describe in detail your RESEARCH METHODS AND CONCLUSIONS. Procedures: Detail all procedures and experimental design including methods for data collection. Describe only your project. Do not include work done by mentor or others. Risk and Safety: Identify any potential risks and safety precautions needed. Data Analysis: Describe the procedures you will use to analyze the data/results that answer research questions or hypotheses.

What should my research plan have? d. Bibliography: List at least five (5) major references (e.g. science journal articles, books, internet sites) from your literature review. If you plan to use vertebrate animals, one of these references must be an animal care reference.

If you have human participants, you will need to include: Participants: Describe who will participate in your study (age range, gender, racial/ethnic composition). Identify any vulnerable Populations: (minors, pregnant women, prisoners, mentally disabled or economically disadvantaged). Recruitment: Where will you find your participants? How will they be invited to participate?

Methods What will participants be asked to do? Will you use any surveys, questionnaires or tests? What is the frequency and length of time involved for each subject?

Risk Assessment Risks. What are the risks or potential discomforts (physical, psychological, time involved, social, legal, etc.) to participants? How will you minimize the risks? Benefits List any benefit to society or each participant.

Protection of Privacy Will any identifiable information (e.g., names, telephone numbers, birth dates, email addresses) be collected? Will data be confidential or anonymous? If anonymous, describe how the data will be collected anonymously. If not anonymous, what procedures are in place for safeguarding confidentiality? Where will the data be stored? Who will have access to the data? What will you do with the data at the end of the study?

Informed Consent Process Describe how you will inform participants about the purpose of the study, what they will be asked to do, that their participation is voluntary and they have the right to stop at any time

If you are using any hazardous material or methods in your project, you will need to include: Hazardous chemicals, activities & devices: • Describe Risk Assessment process and results • Detail chemical concentrations and drug dosages • Describe safety precautions and procedures to minimize risk • Discuss methods of disposal