2 will you tell participants that their participation

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2 Will you tell participants that their participation is voluntary? 3 Will you obtain written consent for participation? 4 If the research is observational, will you ask participants for their con- sent to being observed? 5 Will you tell participants that they may withdraw from the research at any time and for any reason? 6 With questionnaires, will you give participants the option of omitting questions they do not want to answer? © Cardiff University, Centre for Medical Education [First Created 2019] . All Rights Reserved.
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MSc Psychiatry Mock Ethics Application MET464 7 Will you tell participants that their data will be treated with full confiden- tiality and that, if published, it will not be identifiable as theirs? 8 Will you debrief participants at the end of their participation (i.e. give them time a brief explanation of the study)? 9 Will you store the study data (and any related audio recordings) for the appropriate length of time as stipulated by the University guidelines? (- procedures/record-management-policy-and-retention-schedules) If you have ticked No to any of Q1-9, please give an explanation on a separate sheet. (Note: N/A = not applicable) Yes No N/A 10 Will you project involve deliberately misleading participants in any way? 11 Is there any realistic risk of any participants experiencing either physical or psychological distress or comfort? If Yes , give details on a separate sheet and state what you will tell them to do if they should experience any problems (e.g. who they can contact for help). If you have ticked Yes to Q10 or 11 please give a full explanation. Yes No N/A 12 Do participants in your research fall into any of the following special groups? Please note that you may also need to obtain satisfac- tory DBS checks (or equiva- lent for overseas students). School children (under 18 years of age) People with learning or communica- tion difficulties, or vulnerable adults People in custody People engaged in illegal activities (e.g. drug-taking) Yes No 1 3 Is this project “unfunded” (i.e. supported by internal monies)? Please note that for all unfunded projects, it is the lead researcher’s responsibility to provide evi- dence of scientific review. If the answer to the above question is yes, please provide the name of the reviewer. Name: Yes No 1 4 Are there any research governance considerations? (e.g. does the study in- volve, for example: the use of a drug, randomisation/blinding, human tis- sue, implications regarding Data Protection) You will need to contact Re- search Governance before submission ( [email protected] ) Yes No 1 5 Does the study involve the collection or use of human tissue (including, but not limited to, blood, saliva and bodily waste fluids)? If yes, a copy of the submitted application form and any supporting documentation must be emailed to the Human Tissue Act Compliance Team ( [email protected] ). A decision will only be made once these documents have been received.
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