SLaM Involvement Register: administration changes

SLaM are pleased to advise that Sue Folan will be retiring from the Trust on 2 October and will be replaced by Gemma McDonald who will be taking over the role of Involvement Register Co-ordinator for a period of 6 months.  Gemma will be working from 10.00am until 2.00pm from Tuesday to Friday and her email address will be gemma.mcdonald@slam.nhs.uk and her telephone number will be 020 3228 1592.

To ensure a smooth handover, we have put in place certain contingency plans to manage the Involvement Register, as follows.  We would ask for your full co-operation in complying with these measures to ensure that it is ‘business as usual’.

  1.  We will be creating a dedicated Involvement Register email address for you to email your timesheets; travel claim forms (where no original tickets are attached); requests for further supplies of timesheets and travel claim forms; notification of change of address or bank details; payroll queries; requests for a reference, etc. to this email address.  We will notify you as soon as this email address is activated.
  2. You can also hand-deliver timesheets and travel claim forms, together with any other written requests to the Main Reception of the Maudsley Hospital.  The Reception staff will be holding an ‘Involvement Register’ envelope in which you can place your documents.  The envelope will be collected daily.
  3. You can post your timesheets and travel claim forms, together with any other written requests to ‘The Involvement Register, c/o the Post Room, Maudsley Hospital, Denmark Hill, London SE5 8AZ’.
  4. Regrettably, timesheets can no longer be faxed through.
  5. Should you wish to make an appointment to meet with Gemma for any reason, eg. to present your DBS Declaration so that we may capture the details for our records, please do so by emailing her or by calling her on  020 3228 1592.  As the Involvement Register will no longer be based in the HR Department, please do not call into the HR Department after 17 September 2014 for any reason, as you may have done so previously.
  6. In order for Gemma to process your timesheets effectively, please ensure that they contain your name; your assignment number; the week commencing date (to be found in the top right-hand corner of the timesheet); the involvement activity description has been entered against the correct day of the week; the correct timings have been given; a relevant staff member has countersigned the timesheet and applied their respective budget code.  Failure to provide this information on your timesheet may result in delays to your payment(s) .

Thank you for following these arrangements and we hope that they don’t cause you too much disruption.


SLaM Recovery College and the Involvement Register

Hi D,

Apologies you have not received a reply.

I met with Gabrielle and Kirsty last week and I can clarify the following.

In terms of the Recovery College we have clarified there are three types of roles:

  1. Peer Recovery Trainers on Trust contracts (fixed hours):

If you are work for the Recovery College as a peer Recovery Trainer employed directly by the Trust, you can also do other involvement activity to a maximum of 30 hours on the IR per month

i.e. the contracted hours those people work for the recovery college are not included in IR hours.

  1. Associate Peer Recovery Trainers: on Trust contracts with no fixed hours but negotiated on a termly basis – If you work for the Recovery College as an Associate Peer Recovery Trainer employed directly by the Trust you can also do other involvement activity to a maximum of 30 hours on the IR per month

i.e. the contracted hours those people work for the recovery college are not included in IR hours.

  1. Sessional Peer Recovery Trainers: occasional sessional work (for example one workshop per term). These people can be paid through the involvement register and these hours will be part of the 30 hours per month involvement activity.

NB The Recovery College will try not to use ad-hoc self-employed providers unless they are external and we cannot source this expertise from within the Trust. It is intended that people who work for the Recovery College wherever possible, will be employed by the Recovery College for this work and not paid via the IR.

We recognise there will be some individual cases at present where people are applying for associate peer trainers posts who are currently being paid for recovery college work via the IR. We are working with them to bring this in line with the above.

Hope this helps D.

Best wishes

Ann


Biomedical Research Centre

We are looking for representatives to inform the work of the Biomedical Research Centre for Mental Health (BRC-MH). The BRC-MH is based across the Institute of Psychiatry and SLaM, and is funded by the National Institute of Health Research (NIHR). More information about the roles can be found in the attached documents.

Role description_Cluster representatives_Carers

Role description_Cluster representatives_Service users

We are looking for people who can provide a service user or carer perspective to the BRC programme. We are looking for people with an interest in research, and who are committed to improving biomedical research in mental health.

Further information about the BRC can be found on our website: http://brc.slam.nhs.uk/brc-home

 


The Medical Schools Council – Call for Patient Focus Group Participants

The Medical Schools Council is looking for members of the public to take part in focus groups exploring patients’ expectations of doctors and their views on selecting medical students.  Please see below for further information.

Call for Patient Focus Group Participants

Please contact Thomas Marsh at 020 7419 5430 or Thomas.Marsh@medschools.ac.uk

 


Transcranial Magnetic Stimulation (TMS) dicussion group

Hi there,

The Mental Health Foundation is seeking to gather together people who have used mental health services and carers of those who have used mental health services to hear their thoughts, ideas, feelings, comments on the subject of Transcranial Magnetic Stimulation (TMS).

The group will meet on Tuesday 29th July 10:30am – 2:30pm at the Mental Health Foundation (Colechurch House, 1 London Bridge Walk, London, SE1 2SX).

o   participants will be paid £25 each

o   all travel expenses will be covered

o   lunch will be provided

If you are interested in participating, please contact Jo Ackerman at the Mental Health Foundation jackerman@mhf.org.uk and to complete the demographics form (anonymous).

More detailed information is available on request

Thanks so much to everyone who got involved in Mental Health Awareness 2014 – Are you Anxiety Aware?

Watch this Anxiety flashmob for a taste of the great activities people got up to around the UK.


Looking for stories

doorways flyer


MYHEALTHLOCKER TEST DRIVERS NEEDED

Myhealthlocker is an online health record which is managed by YOU, the service user. This means that you can monitor your own health online. Myhealthlocker also contains resources like useful contact numbers, and tools to help with psychosis.

Myhealthlocker is still young and is improving all the time. But we need more people to use myhealthlocker and then give their views on it. Myhealthlocker is likely to be introduced across SLaM, and so this is an opportunity to shape the end product.

There are also some paid opportunities available to test other electronic devices and applications.

If you are interested in finding out more please contact a member of the myhealthlocker team:

Email: myhealthlocker@slam.nhs.uk

Tel: 020 3228 3875

Or you can follow us on Twitter @myhealthlocker


Are you interested in research? Do you want to help improve research opportunities within the Trust?

Over the last two years, we at the Biomedical Research Centre (a partnership between SLaM and the Institute of Psychiatry) have been trying to make it easier for service users to find out about (and participate in) research.

We want to know how well we’ve done, so we are running a brief evaluation exercise across the Trust.

We are looking for service users to help us find out how much people know about research opportunities across the Trust. Participants will be compensated for their time (a fee of £15). This is a brief, one-time activity and all participants will receive detailed feedback. We will also let you know what improvements we will be making as a result of this activity.

We wish to hear from people who:

·         Are currently using SLaM services

·         Have a diagnosis of psychosis

If interested, please contact Konstantina Papoulia at the Institute of Psychiatry (tel: 02078480749; email: konstantina.papoulia@kcl.ac.uk)​


Looking for feedback about a draft Adult Social Care leaflet

Simon Rayner  Head of Mental Health – Southwark Council & Head of Social Care – Southwark/SLaM has asked for some feedback from mental health service users on a draft leaflet about adult social care (personlisation etc).    The leaflet’s purpose is to explain simply and clearly to members of the public what Southwark Adult Social Care can offer, including basic information regarding personalisation, personal budgets, support planning and the customer journey.

Simon would like your views on whether and how the leaflet achieves what it sets out to do, with suggestions for improvements.

There are 2 ways to give feedback:

1)    You can review the leaflet, filling out a review sheet and returning to Simon. For those people on the SLaM involvement register this work could be up to 2 hours paid work at rate PB, could be done from home & needs to be completed by Friday 6th September.

2)    You can look at the leaflet & give general feedback.  This would be a voluntary opportunity and would also need to be completed by Friday 6th September.

To get a copy of the draft leaflet, and for more information please contact:

Alice Glover
Patient & Public Involvement Lead
 – Mood Anxiety & Personality CAG and Psychological Medicine CAG
email:  alice.glover@slam.nhs.uk tel: 020 3228 0959

113 Denmark Hill |The Maudsley Hospital | Denmark Hill | London | SE5 8AZ


Would you like to take part in a group discussion about genetic testing and clozapine? Final Call

My name is Ben Spencer and I am a psychiatry registrar at the Institute of Psychiatry working on a research project that is looking into people’s views of genetic testing in clozapine.

Schizophrenia is a common illness that can affect how people tolerate stress, and their experience of the world.  Some people who have schizophrenia do not get better on standard medication, and treatment with clozapine is offered.  Clozapine can affect the immune system and so people who take it have to have regular blood tests, and sometimes get side effects.

At the moment, researchers are looking into whether it might be possible to use a genetic test to predict if people with schizophrenia would benefit from clozapine, or would get side effects.  This research may mean that people would have to have blood tests less often when they are treated with clozapine.

No one has looked into people’s views on this, and I am keen to find out what people think.  To do this I have written a questionnaire about it to give to people.  I need to find out though if it’s asking the questions that service users think are important.

I am looking for people who have experience of mental health services, and who would like to look at a questionnaire we have written to find out about people’s views and attend a focus group discussion on it.  Ideally if you have knowledge or experience of clozapine or psychosis.

If you wanted to take part I would send you an information sheet about the study, and a copy of the questionnaire for you to complete in your own time.  I would also send you a feedback form so you can write about your experiences of it.

Then I would invite you to come along to a focus group to discuss with other similar people you thoughts on the questionnaire itself (is it too long, short, too simple).  Also at this group we would discuss the research itself and the issues or questions you think we should be asking.

You would be given your travel costs (up to a maximum of £10) to attend the focus group, and a £10 Marks and Spencer’s gift voucher for your involvement.

Please note the focus group session will take place on Thursday  25/07/2013 in Brixton.

Please get in touch if you are interested in being involved in this project by emailing : clozapineandgenes@gmail.com  with your name, phone number, and address to post the study information to.

The deadline to respond by is Wednesday 10/07/2013.


Paid opportunity for two user involvement reps

Hello,

I wonder if you could post this for me? Its for two user involvement reps that are representing the views of patients on the wards at the Maudsley.

Inpatient job description

They can contact me on 0207 358 7030 or suc@lambethandsouthwarkmind.org.uk

Thank you.

Earl Pennycooke

Manager

Southwark User Council

Lambeth and Southwark Mind

Cambridge House

1 Addington Square

London

SE5 0HF


National Audit of Psychological Therapies – Service User Reference Group Recruitment

Data collection for the National Audit of Psychological Therapies for Anxiety and Depression has now been completed and we are busy analysing the data to produce some preliminary findings.

To help develop the recommendations from these preliminary findings we are preparing the data for two different sets of events in June and July:

  • On 27thJune 2013 we are meeting with our Advisory Group Members/Partner Organisations to draft the recommendations, which will form a key part of the National Report and how we take the learning from NAPT forward to make real and enduring improvements in the way psychological therapies are provided.
  • In July, we have planned three Service User Reference Groups to get feedback on whether the preliminary findings fit with service users’ experience and to get feedback on the recommendations we have drafted. Details of these events and answers to frequently asked questions are attached and summarized very briefly below.
Actions to support recruitment – NAPT Service User Reference Groups (July 2013):In order to ensure that these groups are well attended and thus service users’ views are heard we need your help please. We would be grateful if you could:

  • Include information about the groups, their purpose, the eligibility criteria and details of how to register in any publications or on website pages that are read by service users (I am happy to provide a brief couple of paragraphs)
  • Help us recruit through existing service user groups that you are aware of
  • Provide any contact details for service user groups or networks that would be able to help with recruitment
  • Share the attached information with any service users who you think would be interested in taking part
  • Pass these details onto all therapists so that they can share these details with any service users they think would be interested in taking part

We have a deadline of 21stJune 2013 for service users to register so I would appreciate any support in recruitment as soon as possible. Please can you email me with any ideas for recruitment as I am really keen that this vital part of NAPT is as well attended as possible.

Where:

The Service User Reference Groups are being held in London, Manchester and Cardiff

When:

Saturday 6th July in London (10am-1.30pm)

Saturday 13th July in Manchester (10am-1.30pm)

Saturday 27th July in Cardiff (10am-1.30pm)

Purpose:

To share the NAPT preliminary findings with service user’s and get their feedback on whether these fit with their own experience of psychological therapy and use service user feedback to inform NAPT’s recommendations.

Eligibility Criteria:

  • 18 years old or older (there is no upper age limit and we are particularly interested to hear from people over 65 years of age)
  • Currently having or have had psychological therapy/talking treatment for depression and/or anxiety within the past year (this includes therapy for obsessive compulsive disorder (OCD), post traumatic stress disorder (PTSD), phobias or panic attacks)
  • Lives in or near London, Cardiff or Manchester.

Payment for attendance:

We will reimburse service users £50 for their time as well as any reasonable travel expenses. Lunch and refreshments will be provided on the day at no cost to the attendees.

Registration of interest:

Service users can register their attendance in one of three ways:

NAPT SU Reference Groups FAQs July 2013

SU Poster March 29-4-2013 A4


Would you like to take part in a group discussion about genetic testing and clozapine?

My name is Ben Spencer and I am a psychiatry registrar at the Institute of Psychiatry working on a research project that is looking into people’s views of genetic testing in clozapine.

Schizophrenia is a common illness that can affect how people tolerate stress, and their experience of the world.  Some people who have schizophrenia do not get better on standard medication, and treatment with clozapine is offered.  Clozapine can affect the immune system and so people who take it have to have regular blood tests, and sometimes get side effects.

At the moment, researchers are looking into whether it might be possible to use a genetic test to predict if people with schizophrenia would benefit from clozapine, or would get side effects.  This research may mean that people would have to have blood tests less often when they are treated with clozapine.

No one has looked into people’s views on this, and I am keen to find out what people think.  To do this I have written a questionnaire about it to give to people.  I need to find out though if it’s asking the questions that service users think are important.

I am looking for people who have experience of mental health services, and who would like to look at a questionnaire we have written to find out about people’s views and attend a focus group discussion on it.  Ideally if you have knowledge or experience of clozapine or psychosis.

If you wanted to take part I would send you an information sheet about the study, and a copy of the questionnaire for you to complete in your own time.  I would also send you a feedback form so you can write about your experiences of it.

Then I would invite you to come along to a focus group to discuss with other similar people you thoughts on the questionnaire itself (is it too long, short, too simple).  Also at this group we would discuss the research itself and the issues or questions you think we should be asking.

You would be given your travel costs (up to a maximum of £10) to attend the focus group, and a £10 Marks and Spencer’s gift voucher for your involvement.

Please note the focus group session will take place on Thursday  25/07/2013 in Brixton.

Please get in touch if you are interested in being involved in this project by emailing : clozapineandgenes@gmail.com  with your name, phone number, and address to post the study information to.

The deadline to respond by is Wednesday 10/07/2013.


Would you like to take part in a group discussion about genetic testing and clozapine? Final call

My name is Ben Spencer and I am a psychiatry registrar at the Institute of Psychiatry working on a research project that is looking into people’s views of genetic testing in clozapine.

Schizophrenia is a common illness that can affect how people tolerate stress, and their experience of the world.  Some people who have schizophrenia do not get better on standard medication, and treatment with clozapine is offered.  Clozapine can affect the immune system and so people who take it have to have regular blood tests, and sometimes get side effects.

At the moment, researchers are looking into whether it might be possible to use a genetic test to predict if people with schizophrenia would benefit from clozapine, or would get side effects.  This research may mean that people would have to have blood tests less often when they are treated with clozapine.

No one has looked into people’s views on this, and I am keen to find out what people think.  To do this I have written a questionnaire about it to give to people.  I need to find out though if it’s asking the questions that service users think are important.

I am looking for people who have experience of mental health services, and who would like to look at a questionnaire we have written to find out about people’s views and attend a focus group discussion on it.  Ideally if you have knowledge or experience of clozapine or psychosis.

If you wanted to take part I would send you an information sheet about the study, and a copy of the questionnaire for you to complete in your own time.  I would also send you a feedback form so you can write about your experiences of it.

Then I would invite you to come along to a focus group to discuss with other similar people you thoughts on the questionnaire itself (is it too long, short, too simple).  Also at this group we would discuss the research itself and the issues or questions you think we should be asking.

You would be given your travel costs (up to a maximum of £10) to attend the focus group, and a £10 Marks and Spencer’s gift voucher for your involvement.

Please note the focus group session will take place on Wednesday  22/05/2013 in Brixton.

Please get in touch if you are interested in being involved in this project by emailing : clozapineandgenes@gmail.com  with your name, phone number, and address to post the study information to.

The deadline to respond by is Wednesday 15/05/2013.


Would you like to take part in a group discussion about genetic testing and clozapine?

My name is Ben Spencer and I am a psychiatry registrar at the Institute of Psychiatry working on a research project that is looking into people’s views of genetic testing in clozapine.

Schizophrenia is a common illness that can affect how people tolerate stress, and their experience of the world.  Some people who have schizophrenia do not get better on standard medication, and treatment with clozapine is offered.  Clozapine can affect the immune system and so people who take it have to have regular blood tests, and sometimes get side effects.

At the moment, researchers are looking into whether it might be possible to use a genetic test to predict if people with schizophrenia would benefit from clozapine, or would get side effects.  This research may mean that people would have to have blood tests less often when they are treated with clozapine.

No one has looked into people’s views on this, and I am keen to find out what people think.  To do this I have written a questionnaire about it to give to people.  I need to find out though if it’s asking the questions that service users think are important.

I am looking for people who have experience of mental health services, and who would like to look at a questionnaire we have written to find out about people’s views and attend a focus group discussion on it.  Ideally if you have knowledge or experience of clozapine or psychosis.

If you wanted to take part I would send you an information sheet about the study, and a copy of the questionnaire for you to complete in your own time.  I would also send you a feedback form so you can write about your experiences of it.

Then I would invite you to come along to a focus group to discuss with other similar people you thoughts on the questionnaire itself (is it too long, short, too simple).  Also at this group we would discuss the research itself and the issues or questions you think we should be asking.

You would be given your travel costs (up to a maximum of £10) to attend the focus group, and a £10 Marks and Spencer’s gift voucher for your involvement.

Please note the focus group session will take place on Wednesday  22/05/2013 in Brixton.

Please get in touch if you are interested in being involved in this project by emailing : clozapineandgenes@gmail.com  with your name, phone number, and address to post the study information to.

The deadline to respond by is Wednesday 15/05/2013.