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Post InfoTOPIC: Hello Everyone! Hep C Researcher
Heather_Mack
Member

Posts: 6
Date: Mon Sep 21 09:00:46 2009
Hello Everyone! Hep C Researcher


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

__________________

Heather :)

Researching how Health/Social Care professionals are responding to people with Hep C as part of my PhD in Applied Social Science at Lancaster University UK

 

Heather_Mack
Member

Posts: 6
Date: Mon Sep 21 08:44:42 2009

Fantastic! Thank you Deli.

I will send info sheets and start organising dates/times consent and questions with people very shortly.

Very sorry to have not been on here for a couple of weeks - experienced a bit of a delay as I've decided to interview some students about what they know about Hep C too and been organising that with students returning for the new academic year.



__________________

Heather :)

Researching how Health/Social Care professionals are responding to people with Hep C as part of my PhD in Applied Social Science at Lancaster University UK

 

Deli



Veteran Member

Posts: 70
Date: Fri Sep 4 22:40:41 2009

Count me in.

__________________
Genotype 2b pretreatment
Slowly all the roles we act out become our identity. In the end we are what we pretend to be.     Jerry Cantrell
Heather_Mack
Member

Posts: 6
Date: Fri Sep 4 12:48:01 2009

smile That's fantastic, thank you!

Just in the process of refining my questions and then I will be sending them out to everyone who has expressed an interested in taking part.

I'll send you an information sheet on the study through shortly

Heather



__________________

Heather :)

Researching how Health/Social Care professionals are responding to people with Hep C as part of my PhD in Applied Social Science at Lancaster University UK

 

Vectorwoman



Senior Member

Posts: 127
Date: Sun Aug 30 10:29:08 2009

You can count me in for a interview. smile

__________________
We don't need no stinkin' dragons >:o 
 

www.myspace.com/_the_word_
Heather_Mack
Member

Posts: 6
Date: Tue Aug 11 08:46:39 2009

Hi Lau,

Thanks for offering to help with the research that would be fantastic.

Interviews can be done online or by phone. Also if you (or anyone else) would prefer to do it face to face, I'd come to you to make it as easy as possible for you to participate.


Heather

__________________

Heather :)

Researching how Health/Social Care professionals are responding to people with Hep C as part of my PhD in Applied Social Science at Lancaster University UK

 

LaurieBluesGuy



Guru

Posts: 1101
Date: Tue Aug 11 08:22:42 2009

Hi Heather,

if the interviews can be done by phone, on-line, etc then count me in.

Face-to-face would be hard based on our respective locations, but anything I can do to help I will.

Regards

Lau

__________________
Started TX on Jan 07 , Genotype 3a. PCR obtained in July 07. SVR reached Feb 5th 08, B cool and B tough . - Lau http://lauriebluesguy.blogspot.com/
Heather_Mack
Member

Posts: 6
Date: Tue Aug 11 07:35:26 2009

Hi


I really appreciate you asking these questions and giving me the opportunity to clarfiy

a) - ask you to post to the moderators first (just to ensure the questions/survey is appropriate).

I think I should make it clear that I'm not asking to use the forum itself as a research tool. I am recruiting from Hep C services around the UK and I know not everyone uses services (for whatever reason) so the forums enable me to tell people who may not necessarily otherwise find out, what I'm doing and how it's going and therefore they can get in touch if they want to participate in any way - this would be totally voluntary though  -  I understand people here may also not want to contribute directly but still might be interested in what I'm doing and what I've found.

I'm hoping to do one to one interviews with anyone who would like to take part and anyone who expresses an interest in participating would be sent a copy of the interview schedule before the interview goes ahead which would take place seperately away  from the forum so as not to compromise its main purpose.

b) - provide ethical assurances about your research from a supervising lecturer.

I've been through Lancaster University's Ethical Approval process and received approval for the research. I can provide further evidence for this if anyone who would like to see it. I am also waiting to hear back from the NHS Ethics Panel that my research can go ahead and I can recruit in services.

c) - research is done in a an open post - not a private post where appropriate.

I'm happy to be as open and clear as possible and info sheets and anything that did take place on the forum would be conducted openly where appropriate, although obviously protecting participant confidentiality is paramount. Generalised questions might be posed to the forum to give them an idea of what I'm asking but any actual interviews (and arrangements for interviews) would be conducted privately.

I hope this is clear  for everyone and if I can explain anything else any further please do just ask

Heather smile


__________________

Heather :)

Researching how Health/Social Care professionals are responding to people with Hep C as part of my PhD in Applied Social Science at Lancaster University UK

 

LaurieBluesGuy



Guru

Posts: 1101
Date: Thu Jul 23 20:31:08 2009

Hi Heather,

there's no problem with a researcher joining the Forum and asking questions, BUT as a former research student myself we would :-

a) - ask you to post to the moderators first (just to ensure the questions/survey is appropriate).
b) - provide ethical assurances about your research from a supervising lecturer.
c) - research is done in a an open post - not a private post where appropriate.

I know how hard research is and we'd like to help in any way as long as you're happy to comply.

Best Regards

Moderators

__________________
Started TX on Jan 07 , Genotype 3a. PCR obtained in July 07. SVR reached Feb 5th 08, B cool and B tough . - Lau http://lauriebluesguy.blogspot.com/
Heather_Mack
Member

Posts: 6
Date: Thu Jul 23 18:47:30 2009

Hi Everyone,

My names Heather Mack and I'm a research student at Lancaster University UK.

I'm currently working on a research project for my PhD on how Health and Social Care professionals (i.e anyone from GP, Key Workers,  Consultants, Midwives, Social Workers, Nurses, Prison Workers etc.) are responding to people who are living with or who have cleared Hep C.

By joining the forum I'm hoping to
 a) make sure my research stays relevant for the people it's meant to benefit and

 b) to give people who want to, a chance to ask questions/make suggestions about things they think I should consider.

I'm basically hoping to approach people with Hep C to do an interview (which I'm hoping will take place from September if I can get everything ready in time!) about their experiences of living with Hep C and of the support/services they received (or didn't).

Based on what I find I then want to go an ask a range of Health and Social Care professionals about the issues that were deemed important in the interviews with Hep C (all anonymously and confidentially of course) and about how they think they are responding to people with Hep C.

I'm looking for people who might want to talk to me about their experiences of Hep C/services in an interview (I'll post my poster on here too with all the details).

All questions and comments are very welcome and I'll keep you posted with regular updates as I go along so you can see what I've found...



__________________

Heather :)

Researching how Health/Social Care professionals are responding to people with Hep C as part of my PhD in Applied Social Science at Lancaster University UK

 

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