Public Information Pack (PIP) How to get involved in NHS, 1public health and social care research. A quick guide

Similar documents
Patient and public involvement. Guidance for researchers

Co-Production Agreement for Health and Social Care in Hackney and the City of London

This is an Easy Read booklet. This booklet is about changes we want made to social care support for disabled people.

Summary. Exploring Impact: Public involvement in NHS, public health and social care research. Next Page. Kristina Staley I October 2009

Version 1 February Patient and public involvement (PPI) in research groups. Guidance for Chairs

Patient Survey Report Spring 2013

We are currently recruiting new members to advisory groups for the following research programmes:

Recruitment Candidate Guidance

Patient and Public Involvement in JPND Research

Our Pledge to Children in Care and Care Leavers

EasyRead guide to the PowerPoint slides. This is an EasyRead guide to the slides you will see on the screen.

3. How to involve consumers in trials and studies

PPI Panels: Guidance Notes

Plans for chest and lung operations in South Wales

A Guide for Families, Friends and Carers

CRN Wessex Patient Research Experience Survey 2017/18 Report

Adult ADHD Service Patient Information Leaflet

GOC GUIDANCE FOR WITNESSES IN FITNESS TO PRACTISE COMMITTEE HEARINGS

Clinical Trials: Improving the Care of People Living With Cancer

THE DEVOLUTION DIFFERENCE

International Clinical Trials Day is on or around 20 May each year, and commemorates the anniversary of the very first clinical trial by James Lind.

People s Panel today. You can use your views and experiences to help us help other young people.

Your Voices Amplified

Self Harm and Suicide Alertness for professionals working children & young people three month followup. June 2017 October 2017

Appointment of BSL representatives to the British Sign Language (BSL) National Advisory Group. Review Date: November 2017

for healthcare professionals

5: Family, children and friends

NHS 10 year plan Learning disability and autism

Volunteer Handbook. ACLT 2A Garnet Road, Thornton Heath, Surrey CR7 8RD. Tel no: Website:

The Super EDEN Programme A case study illustrating the impact of service user and carer involvement

Janet Rockcliffe and Judith Moreland Aphasia Project Officers

Volunteer Information Pack

Good enough? Breast cancer in the UK

Setting up a Mental Health Support Group

Circles of Support and Mutual Caring

GOC Guidance for Witnesses in Fitness to Practise Committee Hearings

Area Organiser s Handbook

Parkinson s information and support

Treating acute painful sickle cell episodes in hospital

Risk-reducing mastectomy. Preventing infection. Information for patients Information for patients

Bexley Voice Annual General Meeting. 19 th September 2018

The. What-if? Workbook. How to Make Decisions About Your Mental Health Treatment. Ahead of Time. w i t h a d va n c e d i r e c t i v e s

Improving mental health and wellbeing in North West London. Case for Change - a summary

What are the experiences of therapeutic relationships on in-patient wards by people who dissociate?

HANDBOOK. MD MP Contact Program. CANADIAN MEDICAL ASSOCIATION 1867Alta Vista Drive, Ottawa ON K1G 5W

Helping you decide 2014 edition Easy Read

Appendix D. Electronic and Mail Survey Communications

Improving Dementia Services in Northern Ireland. A Regional Strategy

What happens if I cannot make decisions about my care and treatment?

Compliments comments and complaints

Consultation on the role of the Scottish Health Council: Strengthening people s voices in health and social care

Ella Hutchings. Welcome to Winnersh Primary School PTA

Patient Participation Groups

Insight. A message from the Director. In this issue

A practical guide to living with and after cancer. Planning your care and support. Front cover

Research Report Your Thoughts about Sport

Understanding our advice ~ December The use of troponin testing in acute coronary syndromes

Overcoming barriers. Our strategy for

extraordinary fundraising

What is Down syndrome?

A guide to prostate cancer clinical trials

#inyourcorner. Encouraging colleagues to step in

Our plan for giving better care to people with dementia Oxleas Dementia

Keeping control What you should expect from your NHS bladder and bowel service

Good Communication Starts at Home

Dementia Action Alliance survey for carers and professionals

Helping you understand the care and support you can ask for in Wales.

Consultation on the role of the Scottish Health Council

ENABLE Scotland. Edinburgh ACE. Annual Report 2017

If you or one of your relatives has Parkinson s, you may want to know

Worried about someone s mental health?

What are you up to this summer? Be one step ahead of the rest. Take part in the National Citizen Service.

SECTION 3: WHAT DOES DIABETES UK DO?

Watch and wait (active monitoring)

Drumchapel Supported Youth Housing Project Housing Support Service Units 25 & 26 KCEDG Commercial Centre Ladyloan Place Drumchapel Glasgow G15 8LB

Children s Services Involvement Strategy

Our plan for making the lives of people with autism and their families and carers better

Pathfinder Case Study: Engaging with parent carers Case study text (minus headings, contact information etc) should run to a maximum of 3 sides of A4

Love, Sex and You. Love, Sex and You

The Obstetrics and Gynaecology Health Psychology Service

In 2017, we are proud to have supported the following patient organisations:

Planning an event for parents, carers Tand friends

Welcome to Lead Scotland Specialists in Linking Education and Disability

This section will help you to identify and manage some of the more difficult emotional responses you may feel after diagnosis.

Making things better in mental health services. Making things better in mental health services an Easy Read guide to No decision about us without us

Advance Statements. What is an Advance Statement? Information Line: Website: compassionindying.org.uk

Dear Potential Childminder Thank you for your interest in registering as a childminder. Please see the following pages:

A guide to Getting an ADHD Assessment as an adult in Scotland

Safeguarding adults: mediation and family group conferences: Information for people who use services

Speak up. What Healthwatch England did in

SENCO good practice news Winter 2012

GLUTEN-FREE FOOD SCHEME. Information Pack

Volunteer Satisfaction Survey

Contents. Contact information

Scottish Autism - Oban Autism Resources Day Care of Children Lorne Resource Centre Soroba Road Oban PA34 4HY

Recovery from Psychosis: A Ten-Week Program

Secrets to the Body of Your Life in 2017

Voluntary Action Harrow Co-operative. Impact Report

Worcestershire Dementia Strategy

Welcome to the Community Children and Young People s Service. Information you will find useful during your contact with the service

Transcription:

Public Information Pack (PIP) How to get involved in NHS, 1public health and social care research A quick guide

Authors This document was compiled by Kristina Staley, Director of TwoCan Associates (www.twocanassociates.co.uk) and Sam Goold, Public Involvement Officer, INVOLVE, with the help of many other people. This guide should be referenced as: INVOLVE (2018) Public Information Pack (PIP) 1, How to get involved in NHS, public health and social care research - A quick guide. INVOLVE, Southampton. The Public Information Pack (PIP) This guide is the first in a series, all available from INVOLVE: PIP 1: A quick guide a brief introduction to involvement PIP 2: Getting started explaining involvement and what to expect PIP 3: Finding out more the different organisations involved in research PIP 4: Jargon Buster explaining common research terms Introduction This booklet is one of four booklets in INVOLVE s Public Information Pack (PIP). The PIP has been written for patients, carers and members of the public who are interested in getting involved in health or social care research. PIP 1 A quick guide This guide answers the main questions people ask when they first get involved in research. It explains how you can get involved in research, what you can expect and the difference you can make. What is public involvement in research? INVOLVE defines public involvement in research as research being carried out with or by members of the public rather than to, about or for them. Everyone benefits from research. This not only includes scientific research in laboratories, but also research into health and social care. Research provides the evidence about what works best. Patients, carers and health and social care professionals all use this evidence to make decisions about treatments and care. When the public gets involved in research, they work alongside researchers to help shape what research gets done, how it s carried out and how the results are shared and applied in practice. Being involved is not the same as taking part in research. It s not about being the person who takes a new drug in a clinical trial. It s about being a member of the research team that works together to design and run the study. By getting involved in research, you can help make research more relevant and useful to patients, carers and the public. By working with researchers, you will improve research and therefore make a difference to the way health and social care is provided in the future. Today s research is tomorrow s care. Maurice, London Research is defined as a well-ordered investigation or experiment that aims to find new facts and reach new conclusions. Health and social care research aims to find new knowledge that could lead to changes to treatments, policies or care. What can I contribute to research? Your knowledge from having experienced your own care, or the care of others, is of great value to researchers. Researchers may have text book knowledge about different conditions, their treatment and services, but unless they have also lived through it, there will be gaps in their understanding. By contributing your experience and views, you provide valuable expertise that would otherwise be missing. You won t be expected to have technical knowledge of how research works. The knowledge you have as a patient, carer or member of the public is what s unique about your contribution. Have I got the right experience to be involved? There are many different types of research looking at hundreds of different topics. Researchers are likely to want to hear the views of a range people from a variety of backgrounds. This means your experience might be more relevant for some projects than for others. It s about finding the projects that need people like you, and roles that match your interests and experience. Your role is to be a critical friend to researchers. You will see the research from your perspective and advise researchers on how their research could be better. Sometimes this can just seem like common sense to you, but it will be valuable feedback for the researchers. Amander, Southampton 2 3

What difference will I make? You can make a difference at any and every stage of research. Your contributions can help shape the thinking behind the research and the planning and delivery of the project. You have a powerful voice that can influence others beyond the research team, including the people who take part in the research and the people who use the results. Sometimes the involvement of patients, carers and members of the public determines whether a project gets funded, whether it runs successfully and whether the results change practice. What will I be expected to do? When you first get involved, you are likely to be asked to share your thoughts and views on the researchers ideas and plans for their research, and any information written for patients or the public. You might do this in a number of ways, for example by: attending meetings with researchers joining a group of patients, carers and members of the public attached to a research organisation or a specific project becoming a member of a research team commenting on written documents sent to you by post or email Over time you may want to take your involvement further. You can go as far as you want in developing your skills and experience, working at local, regional or national levels, on small or large projects. You may be surprised at the range of opportunities that will be open to you. What can I expect of the people who involve me in their work? You can expect: clear information about what s expected of you and your role a fair and open process of recruitment a good working relationship with the people who involve you regular feedback on how your input has made a difference training and support to enable you to have your say payment for any expenses including travel practical support, such as working in accessible venues a point of contact who can provide information and support on request You may sometimes be offered payment for your time. INVOLVE has produced guidance on payment for involvement, and advice about how this might affect your tax and benefits (both are available online and in paper copies from INVOLVE). What training and support might I be offered? Before you get involved you may be offered training in research or involvement. Depending on your experience, you re likely to find some forms of training more helpful than others. Everyone will have different things they want to learn. There should always be at least one person, and often a team of people, whose job it is to support patients, carers and the public to be involved. They will support you in the way that meets your practical, emotional and information needs, perhaps giving you extra support at the beginning, and helping you to increase your confidence over time. The people who involve you will have invited you to get involved for a reason. They want your input, so they will want to find ways to help you feel able and confident to say what you think. So they will want to support you, to make sure that happens. Helen, Keele Why do researchers want to involve the public in their research? Researchers are aware of the benefits of involvement and therefore want to do it well. They want to learn from their conversations with patients, carers and the public. They will listen to what you have to say and will often make changes to their ideas and plans as a result. They have an added incentive to involve people in their work, because when they apply for funding, they are often asked to state how they have involved patients and the public in developing their proposal, and how they will involve them in carrying out the research. How will I benefit from being involved? People who have been involved in research say that the experience has been more rewarding and more enjoyable than they ever expected. It has given them: a new purpose and a sense of feeling valued new knowledge about how research works and the latest findings new skills as well as opportunities to use existing skills increased confidence a different way to cope with their condition new friends and a source of support 4 5

Why do people decide to get involved in research? People who get involved in research have different reasons for wanting to do it. Some people have had a difficult experience and appreciate being able to do something positive with it. Others have had very good experiences, and see their involvement as an opportunity to give something back. For most people, it s about wanting to make a difference so that in the future, care will be better for the people who come after them. Thanks This quick guide was compiled with the help of a large number of patients, carers and members of the public, as well as staff and researchers with experience of involvement. These people are acknowledged in the PIP 2 Booklet. Very many thanks to all of them for their valuable contributions. I still have my condition, but my experiences and other people s experiences can help to change things. I know what we do makes a difference, maybe not to my health, but to someone else s, to future generations. To be able to be part of that journey by being involved is an amazing thing to do. Diana, Exeter Where can I find out more? You can find out more about public involvement in research from the rest of the INVOLVE Public Involvement Pack which explains involvement in more detail, introduces different research organisations and explains common research terms. Contact INVOLVE for further advice and paper copies of any of their publications: Tel: 023 8059 5628 www.involve.nihr.ac.uk 6 7

INVOLVE is a national advisory group funded by the National Institute for Health Research (NIHR) to support public involvement in NHS, public health and social care research. If you would like to know more about what we do, please contact us: INVOLVE Alpha House University of Southampton Science Park Southampton Hampshire SO16 7NS Web: www.involve.nihr.ac.uk Telephone: 023 8059 5628 Twitter: @NIHRINVOLVE If you need a copy of this publication in another format please contact us at INVOLVE. Telephone: 023 8059 5628 This publication is available to download from: www.involve.nihr.ac.uk Copyright: INVOLVE April 2018