Primary Care Outcomes: Stage 2

  • Research type

    Research Study

  • Full title

    Developing and testing a generic patient-reported outcome tool for primary care

  • IRAS ID

    165882

  • Contact name

    Mairead Murphy

  • Contact email

    mairead.murphy@bristol.ac.uk

  • Sponsor organisation

    University of Bristol

  • Clinicaltrials.gov Identifier

    CT1835, Bristol University Secretary's Office insurance number

  • Duration of Study in the UK

    1 years, 7 months, 1 days

  • Research summary

    In the light of changing service provision across the NHS, including primary care, there is a practical need to assess different forms of service delivery, basing this on outcomes which matter to patients. Such evaluation would benefit greatly from a patient-reported outcome measure (PROM) that is meaningful and relevant to patients and practitioners. A wide-range of PROM tools is available. However, all of these have significant disadvantages as regards their use in primary care service evaluation. A key challenge is that, as the first point of contact for any health-related need, primary care clinicians often address multiple patient problems, with a range of outcomes for each problem.
    This study aims to develop a PROM for primary care which can be used across different models of primary care for use in service evaluations. A separate qualitative study has already been carried out to inform this one. (REC ref: 13/EM/0197). Through that study, 31 outcomes in 3 overall groups were identified as key primary care outcomes. These groups were Health empowerment, Health status and Health perceptions. A systematic review also identified that there were no PROMs available coving all these constructs. This review identified benefits and downsides to two types of PROM: status (measuring how a person is at a point in time) and transitional (measuring how a person has changed over a defined period of time).

    In this study, PROMs will be developed based on the outcomes previously identified. This will be done as follows:
    1. Developing two patient-reported outcome tools (one status and one transitional) and testing the face validity, acceptability and feasibility of these using cognitive interviews;
    2. Testing the validity and reliability of the draft tools to primary care in a cross-sectional sample.

  • REC name

    London - Central Research Ethics Committee

  • REC reference

    14/LO/2236

  • Date of REC Opinion

    9 Dec 2014

  • REC opinion

    Favourable Opinion