Patient Reported Outcome Measure In Skin Cancer Reconstruction Study

  • Research type

    Research Study

  • Full title

    The Patient Reported Outcome Measure In Skin Cancer Reconstruction (PROMISCR) study. Anglicisation and validation of the FACE-Q dermatological surgery outcome measure for patients who have undergone different methods of post-skin cancer reconstruction of the face.

  • IRAS ID

    212618

  • Contact name

    Iain Whitaker

  • Contact email

    iainwhitaker@fastmail.fm

  • Sponsor organisation

    Swansea University

  • Duration of Study in the UK

    2 years, 0 months, 1 days

  • Research summary

    Skin cancer is the most common malignancy worldwide, with 1 in 5 Americans developing skin cancer in their lifetime. It is predicted that the number of skin cancer diagnoses is going to continue to increase year-on-year, with a doubling in number in the next 30 years, along with a fall in the average age of first diagnosis.

    There are a number of treatment options, however surgical excision with a margin of healthy tissue surrounding the lesion is typically favoured in Europe and the USA. The challenge is often not the complete excision of the malignant lesion but the following reconstruction of the defect, especially on the head and neck where cosmesis is clearly important. Reconstructive options include direct closure, skin grafts, local tissue flaps and rarely free flaps. Many factors influence the most appropriate reconstructive option, but in an era where shared-decision making between clinicians’ and patients’ is encouraged it is important that the patient is involved in the discussion regarding the most appropriate reconstructive option. To date very little work has focused on the patient perspective of the difference between these reconstructive options. The aim of this study is therefore to use patient-reported outcome measures (PROMs) to explore patients’ views of the different types of reconstruction available and to investigate if currently available questionnaires are sensitive enough to be used in research and routine clinical practice.

    All eligible patients seen at the Welsh Centre for Burns and Plastics and who are diagnosed with a skin cancer on their head or neck will be invited to take part in the study. Completion of the questionnaire will not affect their clinical management and will not incur any further visits to hospital over and above their routine clinical follow-up. Recruitment will continue for approximately eighteen months.

  • REC name

    West Midlands - Edgbaston Research Ethics Committee

  • REC reference

    16/WM/0445

  • Date of REC Opinion

    3 Nov 2016

  • REC opinion

    Further Information Favourable Opinion