Application for Ethics Approval for MSocScP(SCS) Research Projects Tianyuan Li, Chairperson of the PS Departmental Ethics Committee (May 2015)

Slides:



Advertisements
Similar presentations
The School Research Ethics Committee Welsh School of Architecture.
Advertisements

A Guide. Why is writing an ethics application NOT a waste of time? It helps you to... clarify your research questions. limit your research questions.
Research Skills Participant Recruitment. The Recruitment Process. Before trying to recruit participants you should: Consider research from the point of.
University Research Ethics Committee Workshop on procedure and data protection issues 30th May 2008.
Research Involving Human Subjects All research involving the participation of human subjects must be submitted for review by the IRB (Institutional Review.
7 Tips for Quicker IRB Approval And one unavoidable truth.
Action research, grounded theory and the ethical approval of projects with evolving methods George Ellison Research and Graduate School
Ethical Issues Role of the Qualitative Researcher.
HUMAN RESEARCH ETHICS. TRI-COUNCIL POLICY The University has adopted the Tri-Council Policy Statement on the Ethical Conduct for Research Involving Humans.
Use of Children as Research Subjects What information should be provided for an FP7 ethical review?
Research Compliance Office Consent Form Workshop Kristin B. Frazier HRPP Education Specialist Research Compliance Office January 24, 2008.

The Research Project: ethical approval process
Data Protection Recruitment Process
Registration and Assessment There are 3 periodic assessments throughout the PhD: Assessment 1: the Research Plan (by 8 weeks) All students must complete.
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 March 2015.
Human Subject Research by Students at William Paterson University May 2011.
 About SP ERC  Role of SP ERC  SP ERC Members  ERC Operations  Definition of Research  Definition of Principal Investigator (PI), Co-PI, Collaborator.
Workshop on Health Examination Surveys (HES) Legal and ethical issues Susanna Conti, M. Kanieff, G. Rago Istituto Superiore di Sanità (ISS) (National Public.
Psychology 291 – Lab 4 Ethics October 9, 2012
Human Research Ethics and Obtaining Ethics Approval
NSW Department of Education & Training NSW Public Schools – Leading the Way SELECTION PANEL PROCEDURES FOR SCHOOL TEACHERS 2009 Procedural.
Introducing Research Ethics: Policy and Procedure
What you need to know about the Saint Leo IRB review process.
Institutional Review Board (IRB) Human Subject Dr. John N. Austin, Director and Ms. Renee S. Jones, Associate Director Delaware State University Office.
 The WP IRB is concerned with Social- Behavioral and Biomedical research that is: A systematic investigation Designed to develop or contribute to generalizable.
FAIRTRADE FOUNDATION OCR Nationals in ICT Unit 1 ICT Skills for Business AO2.
1. Proposal deadline 2. Timeline  A grant opportunity announcement will include a sponsor deadline for receipt of the proposal.  The instructions will.
The work of the Research Ethics Committee Dr Carol Chu.
Negotiating access, ethics and the problems of ‘inside’ research.
Information Session for Supervisors.
Teaching Research Methods (Classroom Protocols) Boston University Charles River Campus Boston University Medical Center Mary A. Banks BS, BSN IRB Director.
Canadian English LING 202, Fall 2007 Dr. Tony Pi Research Ethics.
Psychology Departmental Research Ethics Board (Psych-REB) October, 2007 Dr. Pascual-Leone, Chair.
Online ethics review system Peter A. Bath (Deputy Chair, UREC) Peggy Haughton (Minute Secretary, UREC)
Why Proposed TC Procedures? Define how TC reaches “completion” of what OASIS calls “Committee Specifications” TC procedures lead up to the OASIS process:
SUNY Oswego Human Subjects Committee Last Revised 10/28/2011.
Ethical Standards for Conducting Research at Unitec
Fall  Please do not start screening children until they have had 2 weeks to adjust to being in Head Start/ Early Head Start  Screenings are to.
HUMAN SUBJECTS PROTECTION PROGRAM Office Location: 1350 N. Vine Ave. (one block west of Cherry Ave. & three blocks north of Speedway) PO Box Phone:
Human Subjects Protections Research Ethics. Basic Assumptions about How Research Should be Conducted Subjects should be protected from harm. Subjects.
SUNY Oswego Human Subjects Committee Last Revised 10/28/2011.
Institutional Review Board Procedures and Implications After the applied dissertation committee has approved the proposal and the IRB package, the student.
Getting Your Research Through IRB (UCHS) Review Elaine Wethington, Chair Cornell University Committee on Human Subjects (Ithaca)
IRB Applications Ten Common Mistakes. 1. Failing to attach documents properly.
PhD Registration and Assessment procedures There are 3 stages of internal assessment during the PhD: Research Plan 8 weeks after registration date Early.
The IRB Process Southern New Hampshire University.
LEO: LSHTM Ethics Online Patricia Henley Quality & Governance Manager Research Governance & Integrity Office London School of Hygiene & Tropical Medicine.
Created by Steve Martin, PA-C IRB Application Received Exempt Complete Yes No Mississippi College IRB Application Process Determine Review Category Expedited.
Application for Ethics Approval for BEd/BSSc Honours Projects Tianyuan Li, Chairperson of the PS Departmental Ethics Committee (June 2015)
 Empowered by the University to insure we are in compliance with Federal regulations  Guided by the standards in the Belmont Report and regulations.
Lifespan 1 Submission Process to the IRB part 2 Revisions to Protocol.
The research ethics review process Hazel Abbott, Chair University Research Ethics Committee.
Slide 1 Standard Operating Procedures. Slide 2 Goal To review the standard operating procedures Creating the informed consent document Obtaining informed.
SEBE Ethics Information Rod Gameson & Richard Hall.
The Departmental Performance Review Committee
Research Ethics: a short guide for Staff 2017/18
Research Ethics: a short guide for PhD students 2017/18
Registration and Assessment
Duck, Duck, Goose Keeping your IRB Ducks in a Row
Research Ethics Matthew Billington
Top Ten eIRB Application Mistakes
Dr. Niamh Lenahan November 2016
Dr. Sarah Quinton, UREC Chair,
Consent Form Workshop Kristin B. Frazier HRPP Education Specialist
THE FACULTY HIRING PROCESS
UL Research Ethics & Research Integrity
Human Participants Research
PhD Registration and Assessment procedures
Presentation transcript:

Application for Ethics Approval for MSocScP(SCS) Research Projects Tianyuan Li, Chairperson of the PS Departmental Ethics Committee (May 2015)

Review by the Departmental Ethics Committee (DEC), PS DEC Membership: Chairperson and members are appointed by Head. DEC is delegated by Head - to review ethics applications endorsed by supervisors; and - to recommend applications to the Faculty Research and Higher Degrees Committee (FRHDC, FEHD) for approval Enquiries: Miss Helena Tsang, DEC (PS) Secretary,

Student Ethics Application Where to begin? ◦ Departmental ethics application webpage ◦ 37&secid= &secid=2474

Student Ethics Application Documents needed ◦ Application form ◦ Appropriate consent forms and information sheets (e.g., school, parent, participants)  Chinese version also needed if it is the language that will be presented to the participants ◦ (Draft) Questionnaire and/or interview scripts ◦ Research proposal

Procedure Step 1Supervisor to remind student that: - processing time can take 3-4 weeks. For Taught Postgraduate research ethics applications, approval from the Faculty Research and Higher Degrees Committee (FRHDC, FEHD) is required after review by the Departmental Ethics Committee (DEC). - students should NOT start collecting data or asking for participants ’ consent before obtaining approval from the Faculty, and - documents should be downloaded from the Department’s website at Student should read the advice and notes in the application document and reference documents on the web, and consult supervisor in preparing their ethics applications. Step 2Supervisor to review the ethics documents and research proposal prepared by student. Step 3Supervisor to pass the signed application documents to Secretary of the Departmental Ethics Committee (Helena, Soft copy with e-signature is

Procedure Step 4DEC to review and pass feedback comments to student and supervisor for revision. Student is required to use track changes in making changes and pass the revised documents to supervisor. Supervisor to review and forward the documents to DEC for review again. Step 5DEC to review revised application documents. If no further revision is required, DEC Secretary to pass documents to FRHDC (FEHD) for approval. Step 6DEC Secretary to send comments to student and supervisor if FRHDC (FEHD) requests for revision / response / clarification before giving approval. Supervisor to review revised documents first, pass to DEC Secretary for review by DEC, and forward to FRHDC (FEHD) for reconsideration. Approval will be sent to student with a copy to supervisor by: - Faculty Research and Higher Degrees Committee (FRHDC, FEHD) (for Taught Postgraduate research ethics applications)

Time: A major issue! Allow about one month for the ethics application To save time Raise the students’ awareness and help them prepare the documents carefully Only make necessary changes to the templates Draft questionnaire and interview scripts are acceptable as long as experimental procedures will not change in ethically important ways, e.g.: Doesn’t newly ask any potentially sensitive information of the participants (e.g. drug use; sexual activity; etc.), Doesn’t newly recruit children (below age of 18) as participants, Doesn’t introduce new recruitment procedures that could pressure potential participants to participate Doesn’t change anonymity or confidentiality of data (e.g. newly deciding to take videotapes or other recordings)

Common mistakes Information being vague / missing, especially about participants and methodology Number of participants, age range of participants, the way to recruit participants and conduct the study, tasks for the participants, duration of each task, audio/videotape or not, confidentiality/anonymity of the data, etc. Where to store the data? Who can get access to the data? How long the data will be kept for. Information* being inconsistent (initial submission or revision) Consistency between documents: proposal, application form, information sheet, etc Consistency between Chinese and English version of consent form and information sheet * number of participants, duration of task (time commitment), etc. Consent forms and Information Sheets - Mistakes when doing copy and paste. For example, used “your child” in school consent form, used “your student” in parent consent form. - Wrongly placed the names (supervised by [name of student] and conducted by [name of supervisor]) in the forms. - On consent forms, giving information about the purpose of the study, but not giving information about the procedures

Common mistakes Parent consent School consent If there is some kind of potential risk / discomfort or eliciting negative emotion, how to eliminate or minimize More information from the Guideline and FAQs (i) For children aged below 9, only signature of their parents/guardians on consent form is required; completion of the task, after verbal explanation of its nature by the researcher, provides implied consent by the child; (ii) For children aged 9 to 15, signature of both the children and their parents/guardians on consent form is required; and (iii) For adolescents aged 16 to 17, signature of the adolescents on consent form would be required while consent from their parents/guardians is optional for studies involving minimal risk.

Common mistakes Others Application form - PART III, question p “Will the research participant's identity be disclosed if archived tissue samples or personal / medical / social records are used? and PART III, question t “If the study is a medical/clinical research, does the protocol state compliance to declaration of Helsinki ( Normally, the answer to the questions should be “NA”. Some students do not understand the meanings between NA and No. - Part IV, 3a “You will publish this research in the form of … Students should check “Thesis”.

QUESTIONS?