Support for carers of people with early onset dementia
Award Number
ES/L008866/1Programme
Research GrantStatus / Stage
CompletedDates
30 March 2014 -29 September 2017
Duration (calculated)
03 years 05 monthsFunder(s)
ESRC (UKRI)Funding Amount
£201,321.00Funder/Grant study page
ESRCContracted Centre
University of SurreyPrincipal Investigator
Heather GagePI Contact
h.gage@surrey.ac.ukWHO Catergories
Methodologies and approaches for risk reduction researchModels across the continuum of care
Disease Type
Early-onset DementiaCPEC Review Info
Reference ID | 425 |
---|---|
Researcher | Reside Team |
Published | 29/06/2023 |
Data
Award Number | ES/L008866/1 |
---|---|
Status / Stage | Completed |
Start Date | 20140330 |
End Date | 20170929 |
Duration (calculated) | 03 years 05 months |
Funder/Grant study page | ESRC |
Contracted Centre | University of Surrey |
Funding Amount | £201,321.00 |
Abstract
RHAPSODY aims primarily at analysing the health and social care systems and infrastructures in six European countries that are available to the severely burdened yet underserved group of people with young onset dementia (YOD). YOD affects approximately 100 individuals in the population aged 45-64 years and their carers. In addition, RHAPSODY attempts to improve the management of people with YOD by supporting their carers. The main instrument for this will be an educational, web-based, interactive e-learning programme.
A multi-disciplinary team of 8 main investigators from academia and industry representing the fields of psychiatry, neurology, neuropsychology, neuroscience, health economy and information systems as well as a patient and carer advocacy organisation from 6 countries have joined their efforts. They will analyse, evaluate and compare health and social care policies and strategies (macro level) as well as needs and access to service provision and care (individual level). As primary methods documentary analysis, focus groups and qualitative analysis will be employed.
Using this evidence an established key component of dementia management will be tailored to the requirements of the target population of carers with regard to content and format of delivery. An internet-based e-learning programme is particularly appropriate in view of barriers related to low prevalence, geographical spread and reduced mobility.
A pilot study will evaluate the telemedicine intervention with regard to feasibility, acceptance, cost- effectiveness, most appropriate outcomes and effect sizes in 3 countries.
Aims
A multi-disciplinary team of 8 main investigators from academia and industry representing the fields of psychiatry, neurology, neuropsychology, neuroscience, health economy and information systems as well as a patient and carer advocacy organisation from 6 countries have joined their efforts. They will analyse, evaluate and compare health and social care policies and strategies (macro level) as well as needs and access to service provision and care (individual level). As primary methods documentary analysis, focus groups and qualitative analysis will be employed.