NHS and Government Support
Government support for health research outlined in key documents:
2020 Dementia Challenge:
Support has been shown for Dementia and Dementia Research through the Prime Minister’s Challenge on Dementia 2020 publication. In support for Join Dementia Research, the Department of Health sets the following objectives:
1. Every newly diagnosed person with dementia and their carer will receive information on what research opportunities are available and how they can access these through Join Dementia Research.
2. All relevant staff will be able to signpost interested individuals to research via Join Dementia Research.
3. 25 per cent of people with dementia will be registered on Join Dementia Research.
4. 10 per cent of people with dementia will be participating in a research study.
The Challenge Objectives – Join Dementia Research document details the Join Dementia Research components of the 2020 Dementia Challenge.
The Government’s Mandate to the NHS 2018/19 highlights the importance of research as a key deliverable for the NHS, and also support for delivery of the Prime Minister’s Challenge on Dementia 2020.
Guidelines for health and social care professionals, published on 20th June 2018, include a recommendation to tell people living with dementia and their carers about research studies they could participate in. You can read the full NICE guidelines here.
The NHS Constitution published in July 2015, commits the NHS to informing patients about research studies which they may be eligible to participate in.
The Health and Social Care Act 2012:
The Health and Social Care Act received Royal Assent in March 2012. It places unprecedented duties and powers to promote and support research on the Secretary of State and NHS Bodies.
Dementia: Good Care Planning:
In NHS England’s ‘Dementia: Good Care Planning’ document, published in February 2017, Join Dementia Research is mentioned in the ‘Core elements of a care plan’ section, asking if the person living with dementia and their carer(s) have been offered the chance/support to register with the service and /or participate in local research projects.
Memory Service National Accreditation Programme
The Royal College of Psychiatrists’ Centre for Quality Improvement (CCQI) has developed an approach to supporting local service improvement. The Memory Service National Accreditation Programme (MSNAP) applies this approach to memory services. The purpose of MSNAP is to:
- help memory services to evaluate themselves against agreed standards;
- award accreditation to services that meet the required level of performance;
- support local clinical and service improvement in line with the standards;
- produce a local report that highlights achievements and areas for improvement;
- produce a national report which allows a local service to compare its performance against other participating services.
The National Audit Office has recommended that “Primary Care Trusts commission sufficient memory services, which are based on best practice and accredited by the Memory Services National Accreditation Programme”.
The MSNAP Standards for Memory Services asks that memory services:
1. (1.1) the memory service demonstrates that there is a commitment to ongoing quality improvement and research.
2. (1.2.6) the service provides people with dementia and their carers with information about opportunities to participate in local, national and international research, such as National Institute for Health Research (NIHR) portfolio studies or equivalent local bodies (measured in indicator 2).
3. (1.2.7) the service ensures that all people with dementia and their carers are asked if they would like to add their details to a research participation register, e.g. Join Dementia Research (measured in indicator 2).
To meet these standards, memory services are encouraged to review the content of our toolkit. Materials to support promotion and sharing of research opportunities are available free of charge. Visit the Print Resource Ordering Centre to order materials.