Thought I'd post my information sheet on here for people who might like to see it. This is given out to anyone who expresses an interest in taking part in my research
Project:Exploring personal and professional responses to Hepatitis C
Researcher: Heather Mack
PARTICIPANT INFORMATION SHEET
About the researcher:
My name is Heather Mack and I am studying for a PhD in the department of Applied Social Science at Lancaster University. I would like to invite you to take part in my research.
Aims of the research:
The overall aim of the research is to explore the experience of health and social care services, from the perspective of people who are living with (or have cleared) Hepatitis C and from the perspective of health and social care professionals in the field, in order to develop understanding of how the two perspectives can contribute to improved responses to HCV.
The participants role:
I would like to invite you to take part in an interview (either in a group or by yourself, whatever you prefer). The interview will take approximately 1 1.5 hours. I would like to conduct all interviews face to face, but I am happy to conduct individual interviews over the phone or the internet (via email, MSN, or webcam) if that is easiest for you. We can negotiate a suitable time date and place for the interview. I have access to rooms at Lancaster University but would be happy to travel to a location which is most convenient for you.
I intend for the research to have two stages;
Stage 1: Focus groups/interviews with people like yourself, who have experience of living with Hepatitis C and receiving Health and Social care services.
Stage 2: After I have conducted Focus Groups/Interviews I would like to use the general findings to help me develop questions to ask a range of Health and Social Care professionals in interviews. All information you provide will be used anonymously and confidentially.
After these interviews have been carried out I may ask you if you would like to participate in a second focus group/interview to discuss the (anonymous and confidential) findings and how they will be used in the final piece of work and beyond.
Please remember that your participation in this research is entirely voluntary, you have the right to withdraw at any time during the interview process and do not have to give a reason for doing this.
All interviews will take place between September 2009 and August 2010. Before we meet I will send you a copy of the interview questions, so that we can discuss any topics/areas which you might be unsure about.
All interviews will be tape recorded and written out in full (transcribed). During the interview you have the right to stop, start or rewind the tape at any point. The recording will be confidential and I will be the only person who has access to it. After I have transcribed the interview, you will be sent a copy so you have the opportunity to review the transcript and amend your comments.
Before we conduct the interview I will ask you to sign a consent form to show you have received this information sheet and are willing to take part in my research. I will provide you with a copy of the signed form. On this form you will also have the opportunity to choose a different name (pseudonym) which I will then use when quoting you in the final piece of work (thesis) and any publications or reports.
How the interview data will be used:
The information collected during the focus group/interviews will be used as part of my PhD thesis. It might also be used in some future presentations, publications or reports. All information will be used anonymously.
After the first focus group or individual interview I will produce a summary of the main findings and how these have informed the questions for the interviews with health and social care professionals. Please make sure that you have provided the correct email or home address if you would like to receive this. Your comments on this will be welcome.
Confidentiality and anonymity
I will treat all the information you provide as confidential (in accordance with the Data Protection Act 1998). The data you provide will be stored securely in a locked filing cabinet in a locked office on Lancaster University premises. I will be the only person who has access to it. When the research has finished all confidential information will be destroyed.
If you disclose that you intend to cause harm to others or to yourself this will result in a discussion of further action.
The final PhD Thesis and any resulting publications will not contain any information which will identify you as a participant, when you complete the consent form you can choose your own pseudonym, this will be used in the final thesis and any additional publications. This means that you will be able to identify your own contribution to the research but will your identity will still remain anonymous. If you prefer not to pick your own pseudonym, I will choose one on your behalf. Place names will also be provided with pseudonyms in order to preserve participant confidentiality.
Time commitment
The interview will take approximately 1-1.5 hours (excluding travel time, where applicable and breaks). You may also wish to discuss potential questions with me prior to taking part and/or check through your own transcript and take part in a second interview. Therefore I anticipate that the total amount of time required of you, will be approximately 2- 4 hours.
Conduct of the researcher
If you are unhappy with my conduct during the interview process you can contact a person independent of the study; Karenza Moore, Department of Applied Social Science, Bowland North, Lancaster University, Lancaster LA1 4YW. Email: Karenza.moore@lancaster.ac.uk
Sources of support and information
The Hepatitis C Trust helpline: 0845 223 4424
Staffed solely by people with Hepatitis C. This confidential service provides both listening support and information on any aspect of Hepatitis C.
Open 10.30am to 4.30pm Monday to Friday (except Bank Holidays)
Calls cost 3.5p per minute (more if you are calling from a mobile)
If you have access to the internet you can also visit: http://www.hepctrust.org.uk/ for a wide range of information relating to Hepatitis C and details of support.
For queries or worries relating to liver disease.
The British Liver Trust Medical Helpline
The free medical Helpline number is 0800 652 7330 andis open Monday to Friday from 9am until 5pm.
You can also email your enquiry at: info@britishlivertrust.org.uk
For general confidential non-judgmental emotional support, 24 hours a day
Samaritans
Tel: 08457 909090 Email: jo@samaritans.org Write to: Chris, PO Box 9090 Stirling, FK8 2SA
Contact Details
If you would like to ask further questions or would like to take part in the research I can be contacted:
Heather Mack
Department of Applied Social Science
Bowland North
Lancaster University
Lancaster
LA1 4YW
Office telephone: 01524 594118
Email: h.mack2@lancaster.ac.uk
-- Edited by Heather_Mack on Monday 21st of September 2009 09:19:07 AM-- Edited by Minerva on Monday 21st of September 2009 09:33:37 AM __________________