SPaCIS

  • Research type

    Research Study

  • Full title

    Use of the Stroke Patient Concerns Inventory in Stroke Outpatients Clinics: a feasibility cluster randomised controlled trial

  • IRAS ID

    344756

  • Contact name

    Kulsum Patel

  • Contact email

    kpatel@uclan.ac.uk

  • Sponsor organisation

    University of Central Lancashire

  • Duration of Study in the UK

    1 years, 0 months, 31 days

  • Research summary

    Stroke survivors experience ongoing physical, psychological and social concerns affecting quality-of-life. There is a lack of systems and tools that allow healthcare staff to identify stroke survivors’ concerns and so they are often not adequately addressed. Stroke outpatient follow-up appointments are time-limited, reducing opportunity for patients to discuss, and staff to identify, concerns.

    The Patient Concerns Inventory (PCI), is used in cancer-care appointments. The PCI lists potential concerns for patients to select from before their appointment which they would like to discuss. Research shows that using the PCI increased satisfaction with appointments and improved patient quality-of-life, without lengthening appointment time. The PCI has been adapted for stroke (Stroke Patient Concerns Inventory (sPCI)) and a large study is needed to see if it is also effective. Firstly, the study design and the sPCI need to be tested in a smaller study. This study, funded by the NIHR, aims to determine if the sPCI can be used in stroke outpatient services by both staff and patients.

    Four stroke services performing follow-up appointments will recruit a total of 96 participants, who are: stroke survivors within 7-months of stroke, aged 18 years and over, and attending their first follow-up appointment. Two sites will receive training in the sPCI (using it during appointments to discuss concerns and manage them appropriately), and provide their participants the sPCI to complete before their appointment (in addition to their usual practice). The remaining two sites will continue their usual practice.

    Data collection will include: participants’ demographic and stroke information, and quality-of-life at baseline; completed sPCI and participants’ feedback on its use immediately after the appointment; participants’ satisfaction and empowerment within one-week of the appointment; and participants’ quality-of-life and use of health services three-months later. A selection of participants and staff will be interviewed about their experiences of the study.

  • REC name

    Wales REC 3

  • REC reference

    24/WA/0259

  • Date of REC Opinion

    17 Sep 2024

  • REC opinion

    Favourable Opinion