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CHERISH Collaborative for Hospitalised Elders: Reducing the Impact of Stays in Hospital

Do older hospital inpatients admitted to acute care wards implementing the "Eat Walk Engage" quality improvement programme have reduced geriatric syndromes, shorter length of stay and greater likelihood of discharge home than older inpatients admitted to control wards?

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12615000879561
Acronym
CHERISH
Enrollment
1013
Registered
2015-08-21
Start date
2015-10-05
Completion date
2017-03-31
Last updated
2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

Older people (age 65 and older) account for more than half of hospital bed days, and have longer stays and more hospital adverse events that younger people. A hospital stay is often a decisive point in an older person’s health, with hospitalisation accounting for half of newly acquired disability in elders. Geriatric syndromes (including delirium, functional decline, falls, incontinence and pressure injury) result in longer hospitalisations and greater risk of death and institutionalisation. Research clearly shows that “simple” strategies (early mobilisation, adequate oral nutrition, and meaningful cognitive activities) are effective to reduce geriatric syndromes, improve outcomes and reduce costs. While such strategies have been effectively incorporated in specialist “acute care for elders” wards, only a limited number of patients have access to these specialist services. In order to optimise care we need to embed these principles in all acute wards caring for older people. However, this requires systematic changes in acute care staff attitudes, practices and systems of care. We have piloted a programme of enabling facilitation, based on the i-PARIHS implementation framework, to embed this evidence into practice. The “Eat Walk Engage” programme supports a ward-based multidisciplinary team to identify barriers, trial solutions and embed successful strategies into practice using evidence-based quality improvement methods. In two pilot wards at the Royal Brisbane and Women’s Hospital we have shown promising reductions in length of stay, geriatric syndromes and adverse events accompanying process improvements. The CHERISH (Collaborative for Hospitalised Elders: Reducing the Impact of Stays in Hospital) study is a cluster randomised controlled trial of the “Eat Walk Engage” programme across 4 sites, and will provide robust evidence of the transferability, scalability, effectiveness and cost-effectiveness of the programme to inform further implementation. Comparing 4 intervention wards with control wards in the same hospitals to account for other sources of variation, we aim to demonstrate a reduction in hospital stay, geriatric syndromes, and discharge to a higher level of care within 12 months of implementing the “Eat Walk Engage” programme. The project is supported by a Queensland Accelerate Partnership Grant from the Department of Science, Information Technology, Innovation and the Arts, administered by Queensland University of Technology.

Interventions

"Eat Walk Engage" is a quality improvement programme designed to enhance uptake of evidence-based processes of care for older inpatients. The target processes are early mobility; adequate oral nutritional intake; and meaningful, cognitively stimulating activities. The programme uses enabling facilitation based on the i-PARIHS implementation framework, and engages members of the multidisciplinary team on intervention wards to identify barriers to these processes, trial solutions, and embed succes

"Eat Walk Engage" is a quality improvement programme designed to enhance uptake of evidence-based processes of care for older inpatients. The target processes are early mobility; adequate oral nutritional intake; and meaningful, cognitively stimulating activities. The programme uses enabling facilitation based on the i-PARIHS implementation framework, and engages members of the multidisciplinary team on intervention wards to identify barriers to these processes, trial solutions, and embed successful solutions into practice. Solutions may entail both individual behaviour change and system redesign, and are individualised to the context. The facilitator supports change using methods such as marketing, team building, active reflection, process mapping, audit and feedback and education. The facilitator is recruited within the study hospital, but resourced, trained and supported by the project team which includes expert facilitators. This includes a 3 day formal training course; fortnightly in-person or telephone support by the expert facilitator team; 6 monthly forum for sharing skills and experiences between sites; and ad hoc telephone support as required. Facilitator contacts will be monitored by the project manager to measure fidelity. The intervention will take place over 12 months. Facilitator roles include monthly 1-hour group meetings between the site facilitator and the ward multidisciplinary team; identification of local barriers and enablers; facilitation of the planning and implementation of small scale improvement cycles as agreed by the team to support the programme aims; identification of delegation tasks suitable for an additional part time health care assistant resourced by the project; audit and feedback of structured process measures related to the improvement aims (patient interviews, activity audits and mealtime audits); and escalation of barriers and solutions if necessary to higher level decision makers. Meeting minutes and field notes by the novice and expert facilitators will be used to monitor intervention fidelity, and 6 monthly structured process audits will measure implementation effectiveness.

Sponsors

Professor Alison Mudge
Lead SponsorIndividual

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Prevention
Masking
Blinded (masking used) (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
All
Age
65 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Admitted to hospital for 3 or more days, with admission to nominated intervention or control ward

Exclusion criteria

Discharged from hospital within 2 days; palliative intent of care

Outcome results

None listed

Source: ANZCTR · Data processed: Mar 11, 2026