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A rehabilitation intervention to improve recovery after an episode of delirium in adults over 65 years (RecoverED): study protocol for a multi-centre, single-arm feasibility study

Allan, Louise; O'Connell, Abby; Raghuraman, Shruti; Bingham, Alison; Laverick, Abigail; Chandler, Kirstie; Connors, James; Jones, Benjamin; Um, Jinpil; Morgan-Trimmer, Sarah; Harwood, Rowan; Goodwin, Victoria A; Ukoumunne, Obioha C; Hawton, Annie; Anderson, Rob; Jackson, Thomas; MacLullich, Alasdair M J; Richardson, Sarah; Davis, Daniel; Collier, Lesley; Strain, William David; Litherland, Rachael; Glasby, Jon; Clare, Linda

Authors

Louise Allan

Abby O'Connell

Shruti Raghuraman

Alison Bingham

Abigail Laverick

Kirstie Chandler

James Connors

Benjamin Jones

Jinpil Um

Sarah Morgan-Trimmer

Victoria A Goodwin

Obioha C Ukoumunne

Annie Hawton

Rob Anderson

Thomas Jackson

Alasdair M J MacLullich

Sarah Richardson

Daniel Davis

Lesley Collier

William David Strain

Rachael Litherland

Jon Glasby

Linda Clare



Abstract

BackgroundDelirium affects over 20% of all hospitalised older adults. Delirium is associated with a number of adverse outcomes following hospital admission including cognitive decline, anxiety and depression, increased mortality and care needs. Previous research has addressed prevention of delirium in hospitals and care homes, and there are guidelines on short-term treatment of delirium during admission. However, no studies have addressed the problem of longer-term recovery after delirium and it is currently unknown whether interventions to improve recovery after delirium are effective and cost-effective. The primary objective of this feasibility study is to test a new, theory-informed rehabilitation intervention (RecoverED) in older adults delivered following a hospital admission complicated by delirium to determine whether (a) the intervention is acceptable to individuals with delirium and (b) a definitive trial and parallel economic evaluation of the intervention are feasible.MethodsThe study is a multi-centre, single-arm feasibility study of a rehabilitation intervention with an embedded process evaluation. Sixty participants with delirium (aged > 65 years old) and carer pairs will be recruited from six NHS acute hospitals across the UK. All pairs will be offered the intervention, with follow-up assessments conducted at 3 months and 6 months post-discharge home. The intervention will be delivered in participants' own homes by therapists and rehabilitation support workers for up to 10 intervention sessions over 12 weeks. The intervention will be tailored to individual needs, and the chosen intervention plan and goals will be discussed and agreed with participants and carers. Quantitative data on reach, retention, fidelity and dose will be collected and summarised using descriptive statistics. The feasibility outcomes that will be used to determine whether the study meets the criteria for progression to a definitive randomised controlled trial (RCT) include recruitment, delivery of the intervention, retention, data collection and acceptability of outcome measures. Acceptability of the intervention will be assessed using in-depth, semi-structured qualitative interviews with participants and healthcare professionals.DiscussionFindings will inform the design of a pragmatic multi-centre RCT of the effectiveness and cost-effectiveness of the RecoverED intervention for helping the longer-term recovery of people with delirium compared to usual care.Trial registrationThe feasibility study was registered: ISRCTN15676570.

Journal Article Type Article
Acceptance Date Aug 24, 2023
Online Publication Date Sep 15, 2023
Publication Date Sep 15, 2023
Deposit Date Jul 16, 2024
Publicly Available Date Jul 17, 2024
Electronic ISSN 2055-5784
Publisher Springer Verlag
Peer Reviewed Peer Reviewed
Volume 9
Article Number 162
DOI https://doi.org/10.1186/s40814-023-01387-y
Keywords Rehabilitation, Dementia, intervention, Delirium, Feasibility Study, Process Evaluation
Public URL https://nottingham-repository.worktribe.com/output/25645334
Publisher URL https://pilotfeasibilitystudies.biomedcentral.com/articles/10.1186/s40814-023-01387-y
PMID 37715277

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