Post on 29-Dec-2015
AfRE /AREC
IN PARTNERSHIP WITH HRA AND Manchester University
Making an Application to an NHS REC
25th November 2013
Professor Margaret Rees
Chair of Oxfordshire Research Ethics Committee B 2006-2013Member Open University REC 2013- presentSecretary of the Committee of Publication Ethics (COPE)Editor in Chief of MaturitasChair Elect of AfRE
What does an NHS REC look for?
• Is there a checklist?
• Do all RECs view things the same way?
• Why an application might be rejected?
• How to avoid common mistakes.
What is an ethics committee• Expert members• Lay members• Number maximum 18• Quorum 7• Aim is to protect participants• Members need to do regular training • and are audited
Preliminaries
• Reputational Issues: Work as closely as possible with Supervisor prior to sign-off
• University Review, R and D review, external peer review?
• Attendance at REC meetings – Student / Supervisor
• The Meeting
Do all RECs view things the same way?
A checklist:1.Key Ethical issues2.Relevance of the research and research design3.Suitability of applicant and supporting staff4.Quality of Facilities5.Evaluation of anticipated benefits and risks6.Care and protection of research participant
A checklist:
7. Hazards, discomforts and distress of participants
8. Consent of research participant (Including justification for research on persons lacking mental capacity)
9. Participant Information Sheet/ Consent form: Adequacy and completeness
10. Recruitment arrangements11. Confidentiality: Privacy and Protection of
Data12. Indemnity and Compensation
Risk
• Side effects of the intervention eg drugs/surgery
• How many people have received the drug so far
• Radiation: cancer induction no threshold dose of radiation but larger doses increase risk/ damage to a system eg skin burn where there is a threshold dose
• 40-year-old male who underwent coronary angiography, coronary angioplasty and a second angiography procedure due to complications, followed by a coronary artery by-pass graft.
Relevance of the Research and Research design
• Importance of justification – not over justification/ over sell
• Clarity of the science – Lay members
Advertising
• Concerns were raised with regard to the wording of the advertisement, as ‘.........................’ was felt to send a subliminal message and may suggest unreasonable expectations to participants.
Suitability of applicant and supporting staff
• Student / Supervisor
• Risk – Supportive Environment?
• Quality of Facilities ( R and D)
Evaluation of anticipated benefits and risks
• Key element in Risk Assessment
• Management of Risk
• Limits
Care and Protection of Research Participant
• Duty of Care• Supportive Environment – Relevant Permissions• Clarity and Sufficient detail – Participant Information
Sheet/ Consent form• Look at current guidance
Hazards, Discomforts and Distress of Participants
Consent of Research Participant (Including justification for research
on persons lacking mental capacity)
• Consent Form – Relevance / Clarity / Appropriate linkage
with PIS• Conformity with Mental Capacity Act 2005• A Continuing obligation?
Mental capacity • The research is connected with an impairing condition which can affect capacity.• The research cannot be carried out as effectively if it was confined to participants
able to give consent as they would not have the relevant clinical condition.• The research has the potential to benefit participants lacking capacity without
imposing a disproportionate burden on them.• Reasonable arrangements were in place for identifying personal consultees, and
for appointing nominated consultees independent of the project where no person can be identified to act as a personal consultee.
• Information is adequate to enable consultees to give informed advice about the participation of persons lacking capacity.
• Reasonable arrangements are in place for withdrawal from the project
Why an application might be rejected?
• Committee Options• Incomplete paperwork• Key Ethical Themes:• Omitted• Incomplete• Misunderstood / Ignored
• Unsatisfactory responses – commonly through no attendance
• Poor written presentation – particularly the PIS / Consent Form
• Flawed methodology – A Research Ethics issue?
Publication
• Fabrication and falsification
• Lack of ethical approval
• Authorship • Conflict of interest• Plagiarism• Duplicate/ salami slice
submission