Assistive technology and telecare to maintain independent living at home for people with dementia: the ATTILA RCT.

ACTIVITIES OF DAILY LIVING ANXIETY CAREGIVERS COST–BENEFIT ANALYSIS DEMENTIA INDEPENDENT LIVING INSTITUTIONALISATION QUALITY OF LIFE QUALITY-ADJUSTED LIFE-YEARS TECHNOLOGY ASSESSMENT

Journal

Health technology assessment (Winchester, England)
ISSN: 2046-4924
Titre abrégé: Health Technol Assess
Pays: England
ID NLM: 9706284

Informations de publication

Date de publication:
03 2021
Historique:
entrez: 23 3 2021
pubmed: 24 3 2021
medline: 26 10 2021
Statut: ppublish

Résumé

Assistive technology and telecare have been promoted to manage the risks associated with independent living for people with dementia, but there is limited evidence of their effectiveness. This trial aimed to establish whether or not assistive technology and telecare assessments and interventions extend the time that people with dementia can continue to live independently at home and whether or not they are cost-effective. Caregiver burden, the quality of life of caregivers and of people with dementia and whether or not assistive technology and telecare reduce safety risks were also investigated. This was a pragmatic, randomised controlled trial. Blinding was not undertaken as it was not feasible to do so. All consenting participants were included in an intention-to-treat analysis. This trial was set in 12 councils in England with adult social services responsibilities. Participants were people with dementia living in the community who had an identified need that might benefit from assistive technology and telecare. Participants were randomly assigned to receive either assistive technology and telecare recommended by a health or social care professional to meet their assessed needs (a full assistive technology and telecare package) or a pendant alarm, non-monitored smoke and carbon monoxide detectors and a key safe (a basic assistive technology and telecare package). The primary outcomes were time to admission to care and cost-effectiveness. Secondary outcomes assessed caregivers using the 10-item Center for Epidemiological Studies Depression Scale, the State-Trait Anxiety Inventory 6-item scale and the Zarit Burden Interview. Of 495 participants, 248 were randomised to receive full assistive technology and telecare and 247 received the limited control. Comparing the assistive technology and telecare group with the control group, the hazard ratio for institutionalisation was 0.76 (95% confidence interval 0.58 to 1.01; Compliance with the assigned trial arm was variable, as was the quality of assistive technology and telecare needs assessments. Attrition from assessments led to data loss additional to that attributable to care home admission and censoring events. A full package of assistive technology and telecare did not increase the length of time that participants with dementia remained in the community, and nor did it decrease caregiver burden, depression or anxiety, relative to a basic package of assistive technology and telecare. Use of the full assistive technology and telecare package did not increase participants' health and social care or societal costs. Quality-adjusted life-years based on participants' EuroQol-5 Dimensions questionnaire responses were reduced in the intervention group compared with the control group; groups did not differ in the number of quality-adjusted life-years based on the proxy-rated EuroQol-5 Dimensions questionnaire. Future work could examine whether or not improved assessment that is more personalised to an individual is beneficial. Current Controlled Trials ISRCTN86537017. This project was funded by the National Institute for Health Research (NIHR) Health Technology Assessment programme and will be published in full in Many people with dementia living at home are recommended assistive technology and telecare to help them remain living safely and independently in the community. These devices are meant to assist and support activities such as taking medication or cooking, or to raise an alert when there is an issue, such as a fire; however, there is currently little evidence to support such claims. This trial investigated whether or not assistive technology and telecare could delay people moving into residential care and keep them any safer than alternatives, and whether or not they were cost-effective. We recruited 495 people with dementia and their unpaid caregivers, who were randomly assigned to receive either a package of assistive technology and telecare recommended by a health or social care professional or alternative support involving only basic assistive technology and telecare. We monitored the residential status, the use of health-care services and the health and well-being of participants with dementia and their caregivers over a 2-year period. Researchers also spent time with participants to see how they were living with the technology. The trial found no difference in the time that people with dementia with full assistive technology and telecare remained at home, nor any reduction in the number of safety incidents, compared with the participants who received basic assistive technology and telecare only. Full assistive technology and telecare did not increase health and social care costs. It did not improve the well-being of people with dementia or that of their caregivers. People with dementia who had full assistive technology and telecare rated their quality of life poorer than those with basic assistive technology and telecare did, but their caregivers rated their quality of life as about the same as caregivers of people with basic assistive technology and telecare. The technology sometimes averted crises but also disrupted people’s everyday lives. These results suggest that assistive technology and telecare for people with dementia provided in real-world conditions may not be as beneficial as previously claimed. The way that assistive technology and telecare services are organised bears further investigation to see how these services could be improved.

Sections du résumé

BACKGROUND
Assistive technology and telecare have been promoted to manage the risks associated with independent living for people with dementia, but there is limited evidence of their effectiveness.
OBJECTIVES
This trial aimed to establish whether or not assistive technology and telecare assessments and interventions extend the time that people with dementia can continue to live independently at home and whether or not they are cost-effective. Caregiver burden, the quality of life of caregivers and of people with dementia and whether or not assistive technology and telecare reduce safety risks were also investigated.
DESIGN
This was a pragmatic, randomised controlled trial. Blinding was not undertaken as it was not feasible to do so. All consenting participants were included in an intention-to-treat analysis.
SETTING
This trial was set in 12 councils in England with adult social services responsibilities.
PARTICIPANTS
Participants were people with dementia living in the community who had an identified need that might benefit from assistive technology and telecare.
INTERVENTIONS
Participants were randomly assigned to receive either assistive technology and telecare recommended by a health or social care professional to meet their assessed needs (a full assistive technology and telecare package) or a pendant alarm, non-monitored smoke and carbon monoxide detectors and a key safe (a basic assistive technology and telecare package).
MAIN OUTCOME MEASURES
The primary outcomes were time to admission to care and cost-effectiveness. Secondary outcomes assessed caregivers using the 10-item Center for Epidemiological Studies Depression Scale, the State-Trait Anxiety Inventory 6-item scale and the Zarit Burden Interview.
RESULTS
Of 495 participants, 248 were randomised to receive full assistive technology and telecare and 247 received the limited control. Comparing the assistive technology and telecare group with the control group, the hazard ratio for institutionalisation was 0.76 (95% confidence interval 0.58 to 1.01;
LIMITATIONS
Compliance with the assigned trial arm was variable, as was the quality of assistive technology and telecare needs assessments. Attrition from assessments led to data loss additional to that attributable to care home admission and censoring events.
CONCLUSIONS
A full package of assistive technology and telecare did not increase the length of time that participants with dementia remained in the community, and nor did it decrease caregiver burden, depression or anxiety, relative to a basic package of assistive technology and telecare. Use of the full assistive technology and telecare package did not increase participants' health and social care or societal costs. Quality-adjusted life-years based on participants' EuroQol-5 Dimensions questionnaire responses were reduced in the intervention group compared with the control group; groups did not differ in the number of quality-adjusted life-years based on the proxy-rated EuroQol-5 Dimensions questionnaire.
FUTURE WORK
Future work could examine whether or not improved assessment that is more personalised to an individual is beneficial.
TRIAL REGISTRATION
Current Controlled Trials ISRCTN86537017.
FUNDING
This project was funded by the National Institute for Health Research (NIHR) Health Technology Assessment programme and will be published in full in
Many people with dementia living at home are recommended assistive technology and telecare to help them remain living safely and independently in the community. These devices are meant to assist and support activities such as taking medication or cooking, or to raise an alert when there is an issue, such as a fire; however, there is currently little evidence to support such claims. This trial investigated whether or not assistive technology and telecare could delay people moving into residential care and keep them any safer than alternatives, and whether or not they were cost-effective. We recruited 495 people with dementia and their unpaid caregivers, who were randomly assigned to receive either a package of assistive technology and telecare recommended by a health or social care professional or alternative support involving only basic assistive technology and telecare. We monitored the residential status, the use of health-care services and the health and well-being of participants with dementia and their caregivers over a 2-year period. Researchers also spent time with participants to see how they were living with the technology. The trial found no difference in the time that people with dementia with full assistive technology and telecare remained at home, nor any reduction in the number of safety incidents, compared with the participants who received basic assistive technology and telecare only. Full assistive technology and telecare did not increase health and social care costs. It did not improve the well-being of people with dementia or that of their caregivers. People with dementia who had full assistive technology and telecare rated their quality of life poorer than those with basic assistive technology and telecare did, but their caregivers rated their quality of life as about the same as caregivers of people with basic assistive technology and telecare. The technology sometimes averted crises but also disrupted people’s everyday lives. These results suggest that assistive technology and telecare for people with dementia provided in real-world conditions may not be as beneficial as previously claimed. The way that assistive technology and telecare services are organised bears further investigation to see how these services could be improved.

Autres résumés

Type: plain-language-summary (eng)
Many people with dementia living at home are recommended assistive technology and telecare to help them remain living safely and independently in the community. These devices are meant to assist and support activities such as taking medication or cooking, or to raise an alert when there is an issue, such as a fire; however, there is currently little evidence to support such claims. This trial investigated whether or not assistive technology and telecare could delay people moving into residential care and keep them any safer than alternatives, and whether or not they were cost-effective. We recruited 495 people with dementia and their unpaid caregivers, who were randomly assigned to receive either a package of assistive technology and telecare recommended by a health or social care professional or alternative support involving only basic assistive technology and telecare. We monitored the residential status, the use of health-care services and the health and well-being of participants with dementia and their caregivers over a 2-year period. Researchers also spent time with participants to see how they were living with the technology. The trial found no difference in the time that people with dementia with full assistive technology and telecare remained at home, nor any reduction in the number of safety incidents, compared with the participants who received basic assistive technology and telecare only. Full assistive technology and telecare did not increase health and social care costs. It did not improve the well-being of people with dementia or that of their caregivers. People with dementia who had full assistive technology and telecare rated their quality of life poorer than those with basic assistive technology and telecare did, but their caregivers rated their quality of life as about the same as caregivers of people with basic assistive technology and telecare. The technology sometimes averted crises but also disrupted people’s everyday lives. These results suggest that assistive technology and telecare for people with dementia provided in real-world conditions may not be as beneficial as previously claimed. The way that assistive technology and telecare services are organised bears further investigation to see how these services could be improved.

Identifiants

pubmed: 33755548
doi: 10.3310/hta25190
pmc: PMC8020444
doi:

Banques de données

ISRCTN
['ISRCTN86537017']

Types de publication

Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1-156

Subventions

Organisme : Department of Health
ID : 10/50/02
Pays : United Kingdom

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Auteurs

Rebecca Gathercole (R)

Department of Old Age Psychiatry, King's College London, London, UK.

Rosie Bradley (R)

Medical Research Council Population Health Research Unit, University of Oxford, Oxford, UK.

Emma Harper (E)

Medical Research Council Population Health Research Unit, University of Oxford, Oxford, UK.

Lucy Davies (L)

Medical Research Council Population Health Research Unit, University of Oxford, Oxford, UK.

Lynn Pank (L)

Medical Research Council Population Health Research Unit, University of Oxford, Oxford, UK.

Natalie Lam (N)

Medical Research Council Population Health Research Unit, University of Oxford, Oxford, UK.

Anna Davies (A)

School of Health Sciences, City, University of London, London, UK.
Population Health Sciences, University of Bristol, Bristol, UK.

Emma Talbot (E)

Norfolk and Suffolk NHS Foundation Trust, Stowmarket, UK.

Emma Hooper (E)

Lancashire Care NHS Foundation Trust, Preston, UK.
Faculty of Biology, Medicine and Health, University of Manchester, Manchester, UK.

Rachel Winson (R)

Cambridgeshire and Peterborough NHS Foundation Trust, Cambridge, UK.

Bethany Scutt (B)

Department of Old Age Psychiatry, King's College London, London, UK.

Victoria Ordonez Montano (VO)

Hertfordshire Community NHS Trust, Watford, UK.

Samantha Nunn (S)

Cambridgeshire Community Services NHS Trust, Cambridge, UK.

Grace Lavelle (G)

Department of Old Age Psychiatry, King's College London, London, UK.

Matthew Lariviere (M)

Centre for International Research on Care, Labour and Equalities, University of Sheffield, Sheffield, UK.

Shashivadan Hirani (S)

School of Health Sciences, City, University of London, London, UK.

Stefano Brini (S)

School of Health Sciences, City, University of London, London, UK.

Andrew Bateman (A)

School of Health and Social Care, University of Essex, Colchester, UK.

Peter Bentham (P)

Birmingham and Solihull Mental Health NHS Foundation Trust, Birmingham, UK.

Alistair Burns (A)

Faculty of Biology, Medicine and Health, University of Manchester, Manchester, UK.

Barbara Dunk (B)

South London and Maudsley NHS Foundation Trust, London, UK.

Kirsty Forsyth (K)

School of Health Sciences, Queen Margaret University, Edinburgh, UK.

Chris Fox (C)

Norwich Medical School, University of East Anglia, Norwich, UK.

Catherine Henderson (C)

Care Policy and Evaluation Centre, London School of Economics and Political Science, London, UK.

Martin Knapp (M)

Care Policy and Evaluation Centre, London School of Economics and Political Science, London, UK.

Iracema Leroi (I)

Global Brain Health Institute, Trinity College Dublin, Dublin, Ireland.

Stanton Newman (S)

School of Health Sciences, City, University of London, London, UK.

John O'Brien (J)

Department of Psychiatry, University of Cambridge, Cambridge, UK.

Fiona Poland (F)

School of Health Sciences, University of East Anglia, Norwich, UK.

John Woolham (J)

National Institute for Health Research (NIHR) Health & Social Care Workforce Research Unit, King's College London, London, UK.

Richard Gray (R)

Medical Research Council Population Health Research Unit, University of Oxford, Oxford, UK.

Robert Howard (R)

Division of Psychiatry, University College London, London, UK.

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