Pilot implementation of a delirium prevention system of care | Not Recruiting
Pilot implementation of a delirium prevention system of care

Trial Source

There is no location for this trial

Location data is sourced from multiple external providers and UKCTG is not responsible for and cannot guarantee the accuracy of data.

Health Conditions
  • Generic Health Relevance: Age and ageing
Primary Contact Details
Not Recruiting
Recruitment Status
ISRCTN65924234
Primary Trial ID Number
Summary
Background and study aims Delirium, or acute confusional illness, is common in older people. As many as a third of older people who have been admitted into hospital can develop delirium and many people do not fully recover. However, although evidence has shown that there is much that could be done to prevent delirium, the United Kingdom National Health Service does not have routine care systems capable of minimising the impact of this condition. We are undertaking a series of interlinked studies to investigate delirium prevention for older people in hospital. In the first study we worked closely with staff, volunteers and patient and carer representatives from three NHS Trusts to develop a delirium prevention system of care for use in National Health Service hospital wards. We have called this the Prevention of Delirium Programme. The Prevention of Delirium Programme is based on the evidence for delirium prevention and learning from our research partners in the previous study. It involves ward staff and volunteers addressing known modifiable risk factors for delirium (including, for example, infection, pain, poor mobility and sleep disturbance). The basis for this intervention is not a novel treatment approach but attempts to provide a comprehensive system of care that reliably and routinely drives up the standard of general care for vulnerable older patients at risk of delirium on general medical and surgical wards. The aim of the present study, which is the second in our programme of research to investigate delirium prevention for older people in hospital, is to test the Prevention of Delirium Programme system of care in hospital wards to see how well it works and how acceptable it is to patients, carers, volunteers and staff. Who can participate? Managers, staff and volunteers in participating wards and hospitals. Patients who have been admitted to participating wards and their carers. What does the study involve? We will introduce the Prevention of Delirium Programme on at least one ward in each of three hospitals over six months and implement it for a further six months. We will undertake an audit before and after implementation of the Prevention of Delirium Programme to see what impact it has on staff workload. We will assess the impact of the Prevention of Delirium Programme on patients’ satisfaction with care using questions from the national in-patient questionnaire survey. We will interview patients, carers, staff and hospital volunteers to see how acceptable the Prevention of Delirium Programme has been. We will collect data to assess how well the Prevention of Delirium Programme has been used in practice. We will analyse all the data to see how feasible and acceptable the Prevention of Delirium Programme has been and whether we need to alter it. If we find it has been successful, we plan to test the delirium prevention system of care in a future study to see if it reduces delirium. What are the possible benefits and risks of participating? There will be heightened awareness and knowledge of delirium prevention among the staff in the participating wards. The participating wards will be implementing a delirium prevention system of care with potential benefits to patients admitted to those wards – a particularly vulnerable group of patients susceptible to delirium. The Prevention of Delirium Programme is a ward-based quality-improvement programme with minimal associated risk for patients. There are no risks involved to staff and hospital volunteers over and above those associated with their usual ward-based activities. Where is the study run from? The Academic Unit of Elderly Care and Rehabilitation, Institute of Health Sciences, University of Leeds, UK. When is the study starting and how long is it expected to run? The study started in June 2011 and is scheduled to run for 18 months until November 2012. Who is funding the study? Funding has been obtained from the National Institute for Health Research as a Programme Grant for Applied Research. Who is the main contact? Chief Investigator: Professor John Young (john.young@bthft.nhs.uk) Programme Manager: Dr John Green (john.green@bthft.nhs.uk)
Research Details
  • Delirium, or acute confusional illness, is common in older people: as many as a third of hospitalised older people can develop delirium and many people do not fully recover. However, although there is much that could be done to prevent delirium, the NHS does not have routine care systems capable of minimising the impact of this condition. In an ongoing study, we are developing a delirium prevention system of care for use in NHS hospital wards. We now want to test this delirium prevention system of care in hospital wards to see how well it works and how acceptable it is to patients, carers, volunteers and staff. To do this, in cooperation with managers, staff and hospital volunteers, we will introduce the delirium prevention system of care on at least one ward in each of three hospitals over six months and implement it for a further six months. We will undertake an audit before and after implementation of the delirium prevention system of care to see what impact it had on staff workload. We will assess the impact of the delirium prevention system of care on patients’ satisfaction with care using questions from the national inpatient questionnaire survey. We will interview patients, carers, staff and hospital volunteers to see how acceptable the delirium prevention system of care has been. We will collect data to assess how well the delirium prevention system of care has been used in practice. We will analyse all the data to see how feasible and acceptable the delirium prevention system of care has been and whether we need to alter it. If we find it has been successful, we plan to test the delirium prevention system of care in a future study to see if it reduces delirium.
Phase
Not Applicable
Study Design
Pilot observational qualitative trial
Study Type
Observational
Intervention

The intervention is a delirium prevention system of care – the Prevention of Delirium (POD) Programme. The POD Programme is a ward-based, quality improvement programme which will be embedded in usual ward practice. The POD Programme will consist of a multicomponent intervention targeting ten modifiable delirium risk factors in older people in hospital: cognitive impairment / disorientation, dehydration and/or constipation, hypoxia, infection, limited mobility or immobility, pain, polypharmacy.

Intervention Type
Other
Primary Outcome Measures
  • We will undertake a before and after study in each of the case study sites.
Secondary Outcome Measures
  • No secondary outcome measures
Publication(s)
2013 results in: http://www.ncbi.nlm.nih.gov/pubmed/24004917
Result Reports
Sorry, this information is not available
Gender
Both
Age Range
Senior
Who Can Participate
Patient
Number of Participants
Planned Sample Size: 500; UK Sample Size: 500
Participant Inclusion Criteria
  • Hospital staff and volunteers:
  • 1. Introductory workshop and associated follow-up interviews
  • Workshop participants will include patient and carer representatives, hospital managers, clinical and voluntary service managers, volunteers, senior clinicians, nurses and therapists. We will arrange individual followup interviews with purposefully selected staff.
  • 2. Delirium Prevention System of Care Implementation Teams
  • Team members will consist of staff having a potential interest/role in the delirium prevention system of care, e.g. senior manager, senior doctor, matron, nurse consultant and/or specialist nurse, staff nurse, therapist, manager of the volunteer service, volunteer, patient representative, care assistant and ward clerk or housekeeper.
  • 3. Audit of the impact of the intervention on staff workload
  • All members of the participating ward team and volunteers involved in the delirium prevention intervention present on the participating wards during the audit which will occur over six shifts on each participating ward.
  • 4. Acceptability to staff and volunteers
  • Interviews and focus groups with a sample of service managers, staff and volunteers from participating wards.
  • Patients and carers:
  • 1. Patient satisfaction questionnaire
  • Consecutive patients about to be discharged from the participating wards at the start of the implementation phase and during the delivery phase of the intervention.
  • 2. Patient description
  • All patients admitted to the participating wards over the six months of the delivery of the delirium prevention system of care intervention.
  • 3. Audit of the impact of the intervention on staff workload
  • Patients present on the ward at the time of the audit which will occur over six shifts on each participating ward.
  • 4. Acceptability to patients and carers
  • Interviews with a purposeful sample of patients discharged from participating wards and their carers with differing, positive and negative perceptions of care experiences identified through the satisfaction questionnaire
  • 5. Male and femal participants
  • 6. Aged 65 years and over
Participant Exclusion Criteria
  • 1. Patients in a terminal phase of their illness
  • 2. Does not meet inclusion criteria
Trial Location(s)
GSK Investigational Site
Bradford
BD9 6RJ
Trial Contact(s)
Primary Trial Contact
Prof John Young
john.young@bradfordhospitals.nhs.uk
+44 (0)1274 542200
Other Trial Contacts
Sorry, this information is not available
Countries Recruiting
United Kingdom
Scientific Title
Pilot to test implementation feasibility and acceptability of a delirium prevention system of care
EudraCT Number
Sorry, this information is not available
Funder(s)
  • National Institute for Health Research (NIHR) (UK)
Other Study ID Numbers
10652
Sponsor(s)
Bradford Institute for Health Research (UK)
Key Dates

Recruitment Start Date

01 Jun 2011

Recruitment End Date

30 Nov 2012

Trial Start Date

01 Jun 2011

Trial End Date

30 Nov 2012

Date Assigned

29 Jun 2012

Last Updated

30 Jul 2014