ASICA-Achieving Self-directed Integrated Cancer Aftercare in melanoma

  • Research type

    Research Study

  • Full title

    Achieving Self-directed Integrated Cancer Aftercare (ASICA) in melanoma: A randomized patient-focused trial of delivering the ASICA intervention as a means to earlier detection of recurrent and second primary melanoma

  • IRAS ID

    223906

  • Contact name

    Peter Murchie

  • Contact email

    p.murchie@abdn.ac.uk

  • Sponsor organisation

    University Of Aberdeen

  • Duration of Study in the UK

    1 years, 11 months, 30 days

  • Research summary

    Melanoma is common. Approximately 14,500 people in the UK were diagnosed with melanoma in 2013. The incidence of melanoma has increased 360% since the late 1970s. Approximately 20% of patients with early-stage melanoma experience a recurrence and 4-8% develop a new primary melanoma. The risk of having a recurrence or developing a new primary melanoma is highest in the first five years after initial treatment. For this reason, current UK melanoma treatment guidelines recommend that all people treated for melanoma attend regular hospital follow-up appointments to help detect any recurrences or new primaries that may have developed. It is also recommended that patients conduct monthly total-skin-self-examinations (TSSE). The ASICA trial is investigating whether a digital app can help people with melanoma to use a hand-held tablet computer to do more regular and effective total-skin-self-examinations, and whether this would lead to earlier detection of recurrent and new primary melanomas. The ASICA app uses the internet to enable people to electronically communicate the findings of their TSSE. Adult patients (age 18 or over) who have been treated within the preceding 24 months for a stage 0-2C primary cutaneous melanoma and who consent to take part in the trial will be randomised either to the ASICA app in addition to their normal follow-up or to routine follow-up only. We aim to recruit 240 participants across 2 UK NHS Hospitals. The main outcomes of the study are the impact of receiving ASICA on cancer worry (Cancer Worry Scale), anxiety and depression (HADS) and quality of life (EQ-5D) up to 12 months from enrolment.

  • REC name

    North of Scotland Research Ethics Committee 2

  • REC reference

    17/NS/0040

  • Date of REC Opinion

    14 Apr 2017

  • REC opinion

    Favourable Opinion