ࡱ>  Nbjbj ;Hp~_p~_l{d2 < HHH\\\8 #\h)949:99F;<|X=@$ҵɭ1H=F;F;==ɭHH99H2AAA=H9H9A=AA*CQg 9h>?,<h@H==A=====ɭɭ@===h=============X :    IASR Staff and Post Graduate Research Student: Ethics Application Form All IASR staff and Post Graduate Research (PGR) student projects involving people must receive ethical approval via the HYPERLINK "/research-ref/iasr/ethics"IASR Research Ethics Panel. Ethical approval must be obtained before commencing data collection and you must abide by the terms of the approved ethics statement for your research. If the material circumstances of your research changes and unforeseen ethical issues or challenges emerge, you should seek further approval via a  HYPERLINK "/iasr/ethics/forms/" F4 change of research design form. Please attach relevant supporting documentation including information sheets, privacy notice, consent forms and support and complaints sheets (final versions) and research materials (draft versions are acceptable). Ethics approval will not be given without review of this documentation. Ensure all supporting documentation are clearly referenced as appendices within your application. Please answer all relevant questions in terms that can be understood by a lay person and note that your form will be returned if incomplete. Research approved via the IASR Research Ethics Panel must comply with the Universitys  HYPERLINK "/media/84585/research-ethics-policy.pdf" Research Ethics Policy. Please read before completing this application. Fieldwork during Covid-19 Before starting in-person data collection, a ɫƵ (UoB)  HYPERLINK "https://in.beds.ac.uk/media/237759/uob-blank-risk-assessment-hsf-01-a.doc" generic risk assessment must be undertaken and approved before any in-person fieldwork can take place. It is expected that risk assessments comply with relevant Government guidance on social distancing, working arrangements, and travel (in the UK and where the fieldwork takes place, if overseas). The pandemic is on-going and steps can still be taken to reduce the risk of catching and spreading Covid-19. Further guidance and an example of an approved risk assessment is available  HYPERLINK "/iasr/ethics/guidance/" here. The  HYPERLINK "http://www.esrc.ac.uk/funding/guidance-for-applicants/research-ethics/" Framework for Research Ethics produced by the  HYPERLINK "http://esrc.org.uk/" Economic and Social Research Council (ESRC) provides comprehensive guidance on many potential ethical issues during the complete lifecycle of a project and includes information and guidelines on good research conduct and governance. PGR students should complete this form in consultation with their supervisors. Supervisors must sign the declaration at the end of the form. PGR applications will be not be reviewed unless signed by supervisors. Please complete this form and return to  HYPERLINK "mailto:Hemlata.Naranbhai@beds.ac.uk" Hemlata.Naranbhai@beds.ac.uk on the date specified in your advanced notification form to ensure timely review. Further information and accompanying IASR ethics guidelines can be accessed  HYPERLINK "/research-ref/iasr/ethics" here. Research Misconduct: Allegations of Research Misconduct against post graduate (non-taught) research students should be made to the Head of the Research Graduate School. Allegations against staff should be directed to the head of IASR. Office use onlyIASR reference number Section 1: Contact detailsName: FORMTEXT      Contact number/s: FORMTEXT      Email address: FORMTEXT       Section 2: Project detailsProject title: FORMTEXT      Project start date: FORMTEXT      Project end date: FORMTEXT      Data deletion data Specify which professional code of ethics will be adhered to for this research:  FORMTEXT       Is your research funded externally e.g. Department of Health FORMCHECKBOX  Yes  FORMCHECKBOX  NoIf yes, please name funder:  FORMTEXT       Is this application a continuation of a research project that has already received ethical approval? FORMCHECKBOX  Yes  FORMCHECKBOX  NoIf yes, provide details below including the ethics reference number:  FORMTEXT       Will your fieldwork be conducted overseas? Staff: If yes, please ensure that you have read and comply with  HYPERLINK "/about-us/our-university/foi/policies/travel" UoBs policy on conducting business abroad and have obtained insurance via UMAL (the Universitys insurers). Students: If yes, you must check your research is fully covered by the university and your employers or own professional indemnity insurance.  FORMCHECKBOX  Yes  FORMCHECKBOX  NoIf yes, provide details of countries where fieldwork will be undertaken:  FORMTEXT       Does your research require approval from an ethics or research governance committee external to the IASR Ethics Panel? In general, this should only be sought after internal IASR ethical approval has been given. FORMCHECKBOX  Yes  FORMCHECKBOX  No If yes, please list all relevant bodies: FORMTEXT        Do you think that your application requires additional approval by University Research Ethics Committee (UREC)? (see above guidance to determine if your proposal may be subject to UREC approval)  FORMCHECKBOX  Yes  FORMCHECKBOX  No  FORMCHECKBOX  UnsureIf yes, please explain why you think referral to UREC is required: FORMTEXT        Section 3: About youStaff: FORMCHECKBOX  Yes  FORMCHECKBOX  NoPrincipal investigator (PI): FORMTEXT      Co-Investigator/Partners/ Collaborators FORMTEXT      PGR student: FORMCHECKBOX  Yes  FORMCHECKBOX  No Staff details:Staff role: FORMTEXT      Research Centre e.g. Tilda Goldberg Centre (if applicable): FORMTEXT      Research group e.g. Forced migration (if applicable): FORMTEXT       Research degree:Professional Doctorate in Children and Young People's Services (PDCYPS): FORMCHECKBOX Professional Doctorate in Systemic Practice (PDSP): FORMCHECKBOX MPhil/Ph.D.: FORMCHECKBOX MSc by Research FORMCHECKBOX Supervisor name/s: FORMTEXT       Section 4: About your research 4a. Research methods summary (tick all that apply) FORMCHECKBOX  Interviews  FORMCHECKBOX  Focus groups  FORMCHECKBOX  Questionnaires  FORMCHECKBOX  Participatory research  FORMCHECKBOX  Action research  FORMCHECKBOX  Practitioner research  FORMCHECKBOX  Observation  FORMCHECKBOX  Ethnography FORMCHECKBOX  Covert research  FORMCHECKBOX  Case studies  FORMCHECKBOX  Controlled trial/other intervention  FORMCHECKBOX  Use of personal records e.g. case file review  FORMCHECKBOX  Secondary analysis of data  FORMCHECKBOX  Advisory/consultation  FORMCHECKBOX  Literature/systematic review  FORMCHECKBOX  Other, please give details:  FORMTEXT       Please describe the aims and objectives of your research (max. 200-300 words):  FORMTEXT       What are the key research questions?  FORMTEXT       What data collection methods will you use? (please summarise in bullets): FORMTEXT       4b. Research participants (tick all that apply) FORMCHECKBOX  Early years aged 0-4  FORMCHECKBOX  Children aged 5-13  FORMCHECKBOX  Young person aged 14-18 FORMCHECKBOX  Adults (please specific below):  FORMCHECKBOX  Unknown (please specific below):  FORMTEXT       Does your research require approval from gatekeepers to access participants? FORMCHECKBOX  Yes  FORMCHECKBOX  NoIf yes, please list relevant gatekeepers and explain how approval will be managed (for example, processes/applications required; service level agreements; etc.): FORMTEXT       How will participants be recruited (please summarise in bullet points):  FORMTEXT       4c. Disclosure and Barring Service checkIf you are planning to carry out research in schools, or if your research will bring you into contact with children and young people under the age of 18, you will need to have a Disclosure and Barring Service (DBS) check and/or equivalent abroad before you start data collection. If your research involves adults, you should contact the Disclosure and Barring Service to find out if a DBS check is applicable.Have/will the researchers require a DBS check? FORMCHECKBOX  Yes  FORMCHECKBOX  NoPlease record DBS number of each researcher and date of issue: Name: FORMTEXT      DBS no. FORMTEXT      Date of issue: FORMTEXT      Name: FORMTEXT      DBS no. FORMTEXT      Date of issue: FORMTEXT      Name: FORMTEXT      DBS no. FORMTEXT      Date of issue: FORMTEXT       4d. Secondary data analysis (please complete for all secondary analysis)Name of dataset/s FORMTEXT      Owner of dataset/s FORMTEXT       Are the data in the public domain? FORMCHECKBOX  Yes  FORMCHECKBOX  No If no, do you have the owners permission/license? FORMCHECKBOX  Yes  FORMCHECKBOX  No Are the data anonymised? FORMCHECKBOX  Yes  FORMCHECKBOX  NoIf applicable, do you plan to anonymise the data? FORMCHECKBOX  Yes  FORMCHECKBOX  NoDo you plan to use individual level data?  FORMCHECKBOX  Yes  FORMCHECKBOX  NoWill you be linking data to individuals? FORMCHECKBOX  Yes  FORMCHECKBOX  No Will you be conducting analysis within the remit it was originally collected for? FORMCHECKBOX  Yes  FORMCHECKBOX  NoIf yes, please explain original consent processes: FORMTEXT      If no, was consent gained from participants for subsequent/future analysis? FORMCHECKBOX  Yes  FORMCHECKBOX  NoIf yes, please explain consent processes: FORMTEXT      If no, was data collected prior to ethics approval process? FORMCHECKBOX  Yes  FORMCHECKBOX  No 4e. Security-sensitive materialSecurity sensitive research includes: commissioned by the military; commissioned under an EU security call; involves the acquisition of security clearances; concerns terrorist or extreme groups. NB: Research involving security-sensitive material will be subject to review by UREC. Will your project consider or encounter security-sensitive material? FORMCHECKBOX  Yes  FORMCHECKBOX  NoWill you be visiting websites associated with extreme or terrorist organisations? FORMCHECKBOX  Yes  FORMCHECKBOX  NoWill you be storing or transmitting any materials that could be interpreted as promoting or endorsing terrorist acts? FORMCHECKBOX  Yes  FORMCHECKBOX  No Section 5: Ethical issuesPlease state clearly the ethical issues which may arise in the course of this research and how will they be addressed. All issues that apply should be addressed. Some examples are given below. 5a. Participation and informed consentPlease state clearly the ethical issues which may arise in the course of this research and how will they be addressed. All issues that may apply should be addressed.Does the study involve children (anyone under 18 years), potentially vulnerable participants or those who are unable to give informed consent? FORMCHECKBOX  Yes  FORMCHECKBOX  No Are participants volunteering to participate in the research? FORMCHECKBOX  Yes  FORMCHECKBOX  NoIf yes, how will you inform participants about the research and gain their informed consent to participate? FORMTEXT      If you do not intend to gain informed consent, please explain why: FORMTEXT       Will any rewards such as vouchers to say  thank you be offered for participation? FORMCHECKBOX  Yes  FORMCHECKBOX  NoPlease provide details of any rewards for participation and why you think this appropriate.  FORMTEXT       Are participants able to withdraw consent during the life of the research? FORMCHECKBOX  Yes  FORMCHECKBOX  NoPlease provide details of how withdrawal of consent will be communicated to participants and details of any restrictions on withdrawal (e.g. timeframes):  FORMTEXT       Will participants be required to take part in the study without their consent or knowledge at the time (e.g. covert observation of people in non-public places), and / or will deception of any sort be used? FORMCHECKBOX  Yes  FORMCHECKBOX  No FORMTEXT       Will data be retained or archived for use by you or other researchers? FORMCHECKBOX  Yes  FORMCHECKBOX  NoIf yes, please state archive location and what safeguards and processes are in place to support long-term retention, including periodic monitoring and review? FORMTEXT       5b. Confidentiality and anonymity What are the boundaries of confidentiality and how will this be explained to participants? For example, how will safeguarding procedures be explained? FORMTEXT       Are data/will data be anonymised?  FORMCHECKBOX  Yes  FORMCHECKBOX  NoIf yes, how will this be explained to participants? FORMTEXT      If no, how will you ensure anonymisation participant data is ensured? FORMTEXT       Will lists of identity numbers or pseudonyms linked to names and/or addresses be stored securely and separately from the research data? FORMCHECKBOX  Yes  FORMCHECKBOX  NoIf yes, where and how will this be stored? FORMTEXT       5c. Safeguarding in the research contextHow will you respond to any safeguarding issues that arise through the research? Please explain your safeguarding procedure for the protection of children, young people or adults at risk of significant harm identified during research: FORMTEXT       5d. Researching sensitive topicsWill the study be exploring sensitive topics (e.g. sexual activity, drug use, ethnicity, political behaviour, potentially illegal activities)? FORMCHECKBOX  Yes  FORMCHECKBOX  NoPlease provide an outline describing the sensitive topics covered and what steps you will take to ensure to recognise, reduce and respond to the potential to cause distress to participants. FORMTEXT       Is there any risk to the physical safety of participants involved in this study? FORMCHECKBOX  Yes  FORMCHECKBOX  NoPlease outline any risks in how participants are contacted and what practical steps will be taken to minimise the risk? FORMTEXT       Are appropriate personal and confidential support services in place to support participants? FORMCHECKBOX  Yes  FORMCHECKBOX  NoPlease detail the support services available to participants. Please any outline immediate and longer-term support needs. FORMTEXT       5e. Involving people with lived experiences/service users Does your research focus explicitly on people with lived experiences/service users?  FORMCHECKBOX  Yes  FORMCHECKBOX  No If yes, please describe the way you have involved people with lived experiences/ service users in your research/ evaluation, including how you will involve them in the conduct of the study and in dissemination and implementation of findings: FORMTEXT      If your research/evaluation focuses on people with lived experiences/service users or practitioners and you are NOT directly involving them, please justify/explain your reasoning:  FORMTEXT        5f. Data protection and security (please refer to UoB general policies on  HYPERLINK "https://in.beds.ac.uk/media/256442/gdpr-staff-guidance.pdf" GDPR, HYPERLINK "https://in.beds.ac.uk/general-data-protection-regulation/guidance-for-researchers/"Guidance for Researchers,  HYPERLINK "https://in.beds.ac.uk/governance/legal/dp" Data Protection and Security and  HYPERLINK "https://in.beds.ac.uk/media/256441/guidance-on-storing-and-transferring-personal-datav2.pdf" Storing and Transferring Personal Data and ensure that you include all hard and electronic data when completing this section). Please note that research projects that process large amounts of personal data, any sensitive data or data of vulnerable individuals require a Data Protection Impact Assessment (DPIA). DPIAs are completed independently of the IASR ethics process and should be submitted to UoBs Data Protection Officer for review at  HYPERLINK "mailto:DPO@beds.ac.uk" DPO@beds.ac.uk. Please ensure you have consulted UoBs  HYPERLINK "https://in.beds.ac.uk/__data/assets/pdf_file/0006/589002/DPIA-Guidance.pdf" DPIA Guidance to check if your project triggers a DPIA.  Does your research require a DPIA?  FORMCHECKBOX  Yes  FORMCHECKBOX  No Please record DPIA number and date of issue:DPIA no. FORMTEXT      Date of issue: FORMTEXT       The IASR  HYPERLINK "https://www.beds.ac.uk/research-ref/institutes/iasr/ethics/guidance/" Privacy Notice should be provided to all research participants. This details how and why the University uses personal data for research, the Universitys lawful basis for processing data, participant rights and university contact for questions or concerns about the use of personal data. This should be provided in addition to information sheets and it is best practice to ask participants to sign via consent forms to say that they have received.  Do you plan to collect special category data (HYPERLINK "https://ico.org.uk/for-organisations/guide-to-the-general-data-protection-regulation-gdpr/key-definitions/"GDPR definition)? The GDPR definition of special category data includes: ethnic origin; political opinions; religious beliefs or philosophical beliefs; sex life or sexual orientation; health data (physical or mental health as well the provision of health care services; trade union membership; genetic or biometric information (where used for ID purposes). For this sort of data, researchers must have both a valid lawful basis, and a special condition to process this type of data.  FORMCHECKBOX  Yes  FORMCHECKBOX  No If yes, please list:  FORMTEXT       What steps have you taken to ensure that only  special category data which are essential to the research are collected? FORMTEXT       To prevent accidental disclosure of data, how and where will the data be stored both during and after the research e.g. by encryption of data on laptops and memory sticks, password protected documents and folders, not taking printed confidential materials out of premises, storing files in locked cabinets in locked rooms?  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Please use UoB s  HYPERLINK "https://in.beds.ac.uk/media/256444/data-breach-reporting-form.pdf" Data Breach Form and refer to UoB s  HYPERLINK "https://in.beds.ac.uk/media/256443/data-breach-process.pdf" Data Breach Process for more information. Who will have access to the data? This includes, for example, research staff and transcribers? Please note that a data sharing agreement should be signed with transcribing services. If required, the Legal Office can assist with this. FORMTEXT       What steps have you taken to ensure that any transfer of data is secure e.g. physical transfer of research materials from research sites to University and / or electronic transfer of data? FORMTEXT       Will personal data be processed or be sent outside the European Economic Area? FORMCHECKBOX  Yes  FORMCHECKBOX  No If yes, please confirm that there are adequate levels of protections in compliance with the GDPR and state what these arrangements are:  FORMTEXT        For further information regarding data being processed or sent outside the EEA, please refer to guidance produced by the Information Commissioner s Office (ICO) on  HYPERLINK "https://ico.org.uk/for-organisations/guide-to-data-protection/guide-to-the-general-data-protection-regulation-gdpr/international-transfers/" international transfers of personal data. This is also covered via UoB s HYPERLINK "https://in.beds.ac.uk/general-data-protection-regulation/guidance-for-researchers/"Guidance for Researchers. 5g. Research outside the UKIf the work involves data collection outside the UK, are there any special ethical issues arising because of the country/ies where the work takes place? FORMCHECKBOX  Yes  FORMCHECKBOX  No If yes, please outline and steps taken to address issues arising:  FORMTEXT       Is this your normal place of work/ residence? If not, have you carried a full  HYPERLINK "https://www.beds.ac.uk/about-us/our-university/foi/policies/travel" risk assessment as per UoB policy?   FORMCHECKBOX  Yes  FORMCHECKBOX  No  FORMCHECKBOX  Yes  FORMCHECKBOX  No If yes, attach full risk assessment. Are there additional permissions/authorisations that need to be obtained? This includes any local ethics approvals.  FORMCHECKBOX  Yes  FORMCHECKBOX  No If yes, please list:  FORMTEXT       For further information regarding data being processed or sent outside the EEA, please refer guidance produced by the Information Commissioner s Office (ICO) on  HYPERLINK "https://ico.org.uk/for-organisations/guide-to-data-protection/guide-to-the-general-data-protection-regulation-gdpr/international-transfers/" international transfers of personal data. 5h. Researcher well-being and safetyHave any potential physical and/or psychological harm to researchers, for example, lone working? FORMCHECKBOX  Yes  FORMCHECKBOX  No If yes, please outline the practical steps to be followed to minimise risk of physical and psychological harm to researchers:  FORMTEXT        FORMTEXT       If relevant, have appropriate personal and confidential support services been put in place to support research staff undertaking the research? FORMCHECKBOX  Yes  FORMCHECKBOX  No If yes, please detail the support services available to researchers:  FORMTEXT        FORMTEXT       5i. ComplaintsIs it clear who any complaints raised by research participants should be directed to? (In the case of PGR students, this is normally your supervisor) FORMCHECKBOX  Yes  FORMCHECKBOX  No Please provide details of the complaints processes and include via the information sheets - e.g. who should participants contact in the event of a complaint?  FORMTEXT         FORMTEXT       5j. On-going reviewDo you have internal research governance procedures in place to monitor and review progress of any research ethical challenges if and when they arise within the research? FORMCHECKBOX  Yes  FORMCHECKBOX  No Please outline on-going review processes to ensure research is conducted in line with university ethics policy and maintain research integrity e.g. regular research supervision?  FORMTEXT       Significant changes to research design that require further ethical approval should be submitted via IASR Ethics Panel  HYPERLINK "https://www.beds.ac.uk/research-ref/institutes/iasr/ethics/forms/"  change of research design that requires ethical approval . 5k. Publication and dissemination activitiesWho will you inform about the findings of the research, and how? Please refer to all stakeholders, including research participants. FORMTEXT       5l. Other ethical issuesAre there any other ethical issues pertinent to your project that are not covered by the questions above? Please state them clearly and how will they be addressed during the course of the research.  FORMTEXT       5m. Conflicts of interestAre there any real or potential conflicts of interest associated with your research? FORMCHECKBOX  Yes  FORMCHECKBOX  No If yes, please state any conflict(s) identified and steps taken to manage the conflict(s) of interest effectively in order that it does not compromise the integrity of the project: FORMTEXT       Section 6: Attachments: Please attach the following items to the form or explain if not attached. Please note that incomplete forms will be returned.Information sheets, consent forms, IASR privacy notice and other materials to be used to inform potential participants about the research. FORMCHECKBOX  Yes  FORMCHECKBOX  No Please list attachments below FORMTEXT      Research materials, interview schedules, questionnaires etc. FORMCHECKBOX  Yes  FORMCHECKBOX  No Please list attachments below FORMTEXT       If applicable:External Research Ethics Committee approval letter FORMCHECKBOX One-page summary of the proposal for PGR students, evidence the proposal has been approved by PGR Supervisors. FORMCHECKBOX Contracts or agreements with relevant gatekeepers, services, etc. FORMCHECKBOX Full risk assessment FORMCHECKBOX  Section 7: Declaration I confirm that to the best of my knowledge the information in this form is correct and that this is a full description of the ethical issues that may arise in the course of this project. I understand that I cannot begin any fieldwork until the application referred to in this form has been approved by all relevant parties. I agree to carry out the research in the manner specified. If I make any changes to the approved method I will seek further ethical approval for any changes. Signature: FORMTEXT      Date: FORMTEXT       Signature of doctoral supervisor/Director of Studies: FORMTEXT      Date: FORMTEXT       Note to supervisors: Signing this form certifies that in your opinion, the project described here is ethical under university and IASR guidelines. Do NOT sign if you are unsure or if the student has not attached complete details of the research design and methodology. Submission of applicationsPlease save this form as word document using the following convention: Applicantsurname_IASR_RIEPapp_MMMYY.doc (eg Ahmed_IASR_RIEPapp_Feb18) Forward electronic copy of this form to:  HYPERLINK "mailto:hemlata.naranbhai@beds.ac.uk" hemlata.naranbhai@beds.ac.uk clearly stating  Ethics Approval Application and include your surname. TimescalesThe ethical review process takes a minimum of 4 weeks. Any amendments that need to be made by the applicant after initial review will add to this time period. If approval from UREC is required, this may extend the timeline. Please ensure that you allow ample time for ethical clearance. Please note that the above are guidelines for response times which will vary depending on the quality of the application and the number of applications being processed. All applications are assessed prior to forwarding to the IASR Ethics Panel and incomplete applications will be returned for further detail. DecisionsApproved (no conditions): The research is fully approved and can commence immediately (subject to any additional, external approvals required, such as ADCS  see guidance above). Approved with minor advice to applicant for consideration (but there is no requirement to resubmit): The application is approved but reviewers have offered some helpful advice that the applicant may want to consider with their team (if staff member) or supervisor (if student) Conditional: The application needs further work, raises concerns or is incomplete and needs revision and resubmission to RIEP. Research may not commence until this occurs and formal approval from RIEP is given. Unsuccessful: The application is considered to raise fundamental concerns that means it cannot be approved.  This form is based on ethics materials produced by HYPERLINK "https://www.csacentre.org.uk/about-us/research-ethics-committee/"Centre for expertise on child sexual abuse,  HYPERLINK "http://www.ucl.ac.uk/srs/research-ethics-committee/pages/ioe" Institute for Education and  HYPERLINK "http://www.sussex.ac.uk/staff/research/governance/apply" University of Sussex.      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