Delirium prevention for older people in hospital: a feasibility study

  • Research type

    Research Study

  • Full title

    Prevention of delirium for older people in hospital: a cluster, randomised feasibility study of the Prevention of Delirium (POD) Programme versus usual care

  • IRAS ID

    89599

  • Contact name

    John Young

  • Contact email

    john.young@bthft.nhs.uk

  • Sponsor organisation

    Bradford Teaching Hospitals NHS Foundation Trust

  • Research summary

    This 2-year cluster randomised feasibility study seeks to explore the clinical and cost-effectiveness of the Prevention of Delirium (POD) system of care, and to gather data to inform a possible future larger study. It is the third and final study of a Programme Grant for Applied Research funded by the National Institute for Health Research investigating the prevention of delirium in older people in hospital.

    Delirium, or acute confusion, is the most common complication for older people admitted to hospital. Patients with cognitive impairment are especially vulnerable. Evidence suggests that multi-component interventions may reduce delirium in vulnerable patients by a third.

    POD, a multi-component delirium prevention intervention designed and tested in the previous projects of the Programme Grant, is designed to be delivered by ward staff and trained, supervised volunteers. It targets modifiable clinical risk factors for delirium (such as immobility, sleep deprivation, dehydration and pain) in vulnerable patients.

    We aim to recruit 16 elderly care and orthopaedic wards in eight hospitals. Half the wards will be randomised to deliver POD and half to continue with standard care practice (cluster randomisation). All patients admitted to participating wards will therefore receive POD or standard care depending on randomisation.

    We aim to recruit 720 patients who are 65 years or older and who do not have delirium on admission from participating wards over six months.
    Recruited participants will be asked to provide baseline data and will be assessed daily for up 10 days and again at 30 days to determine whether they have delirium. Quality of life, experience of care, and patient mood questionnaires will be undertaken at 30 days. At three months post admission to the ward participants will be sent quality of life, extended activities of daily living and health and social care use questionnaires.

  • REC name

    Yorkshire & The Humber - Leeds West Research Ethics Committee

  • REC reference

    13/YH/0400

  • Date of REC Opinion

    22 Jan 2014

  • REC opinion

    Further Information Favourable Opinion