Prostate Cancer UK Module2 - Phase 2: Post-operative continence care

  • Research type

    Research Study

  • Full title

    Prostate Cancer UK Module2 (Phase 2) Post-radical prostatectomy continence management intervention: Randomised feasibility study

  • IRAS ID

    199429

  • Contact name

    Catherine Murphy

  • Contact email

    c.murphy@soton.ac.uk

  • Sponsor organisation

    University of Southampton

  • Duration of Study in the UK

    0 years, 10 months, 28 days

  • Research summary

    This application refers to Phase 2 (of a 2 phase study) of work aimed specifically at improving the continence care received by men who have undergone radical prostatectomy.
    Research has shown that people would prefer to have a wider choice of products to manage their incontinence than is generally available through their continence service. The products provided by continence service do not reflect the range of options available to patients, do not appear to offer best value, do not best serve patients’ requirements and do not offer choice to patients and their carers.

    In Phase 1, it was established that men who are incontinent of urine due to prostate-related surgery often to not receive any continence support or products from community services and that there is a gap in provision from acute to community care. In response to findings from Phase 1, a Product Decision Aid (PDA) has been developed with the aim of helping patients, carers and clinicians choose appropriate continence products.

    The proposed study will test the feasibility of undertaking a full-scale study to evaluate the effectiveness of implementing a continence management intervention (comprising the PDA, continence product advice and the provision of continence products) at improving the continence-related experiences of men post-radical prostatectomy.

    Initial pre-testing of the PDA will be undertaken in a 2-arm evaluation, with Arm A (n=20) receiving usual care and Arm B (n=20) receiving usual care, plus the PDA. This will be followed by a 3-armed randomised feasibility study of the continence management intervention with men following radical prostatectomies.

  • REC name

    South Central - Berkshire Research Ethics Committee

  • REC reference

    16/SC/0150

  • Date of REC Opinion

    24 Mar 2016

  • REC opinion

    Favourable Opinion