The Achieving Self-directed Integrated Cancer Aftercare Intervention for Detection of Recurrent and Second Primary Melanoma in Survivors of Melanoma: Pilot Randomized Controlled Trial.

Peter Murchie, Lynda Constable, Susan Hall, William Brant, Julia Allan, Marie Johnston, Judith Masthoff, Amanda Lee, Shaun Treweek, Dolapo Ayansina, Charlotte Proby, Kaz Rahman, Fiona Walter, Nigel Burrows, Amer Durrani, Graeme Maclennan
Author Information
  1. Peter Murchie: Institute of Applied Health Sciences, University of Aberdeen, Aberdeen, United Kingdom. ORCID
  2. Lynda Constable: Institute of Applied Health Sciences, University of Aberdeen, Aberdeen, United Kingdom. ORCID
  3. Susan Hall: Institute of Applied Health Sciences, University of Aberdeen, Aberdeen, United Kingdom. ORCID
  4. William Brant: NHS Grampian, Aberdeen, United Kingdom. ORCID
  5. Julia Allan: Institute of Applied Health Sciences, University of Aberdeen, Aberdeen, United Kingdom. ORCID
  6. Marie Johnston: Institute of Applied Health Sciences, University of Aberdeen, Aberdeen, United Kingdom. ORCID
  7. Judith Masthoff: Department of Information and Computing Sciences, Universiteit Utrecht, Utrecht, Netherlands. ORCID
  8. Amanda Lee: Institute of Applied Health Sciences, University of Aberdeen, Aberdeen, United Kingdom. ORCID
  9. Shaun Treweek: Institute of Applied Health Sciences, University of Aberdeen, Aberdeen, United Kingdom. ORCID
  10. Dolapo Ayansina: Institute of Applied Health Sciences, University of Aberdeen, Aberdeen, United Kingdom. ORCID
  11. Charlotte Proby: Molecular and Clinical Medicine, School of Medicine, University of Dundee, Dundee, United Kingdom. ORCID
  12. Kaz Rahman: NHS Grampian, Aberdeen, United Kingdom. ORCID
  13. Fiona Walter: Wolfson Institute of Preventive Medicine and Institute of Population Health Sciences, London, United Kingdom. ORCID
  14. Nigel Burrows: Cambridge University Hospitals NHS Foundation Trust, Cambridge, United Kingdom. ORCID
  15. Amer Durrani: Cambridge University Hospitals NHS Foundation Trust, Cambridge, United Kingdom. ORCID
  16. Graeme Maclennan: Institute of Applied Health Sciences, University of Aberdeen, Aberdeen, United Kingdom. ORCID

Abstract

BACKGROUND: Melanoma is common with increasing incidence. Guidelines recommend monthly total skin self-examinations (TSSEs) by survivors to detect recurrent and new primary melanomas. TSSE is underperformed despite evidence of benefit.
OBJECTIVE: This study compares the effect on psychological well-being and TSSE practice of a self-directed digital intervention with treatment as usual in patients treated for a first stage 0 to IIC primary cutaneous melanoma within the preceding 60 months.
METHODS: This randomized clinical trial was conducted at 2 UK National Health Service hospitals (Aberdeen Royal Infirmary, Grampian, and Addenbrooke's, Cambridge). Adults (≥18 years) diagnosed with a first 0 to IIC primary cutaneous melanoma were randomized to receive Achieving Self-directed Integrated Cancer Aftercare (ASICA), a tablet-based intervention prompting and supporting TSSE in survivors of melanoma, or to usual care. The hypothesis was that ASICA would increase TSSE practice in users affected by melanoma and compared with controls without affecting psychological well-being. The main primary outcomes were melanoma worry (Melanoma Worry Scale), anxiety and depression (Hospital Anxiety and Depression Scale), and quality of life (EQ-5D-5L) as well as secondary outcomes collected using postal questionnaires 3, 6, and 12 months following randomization.
RESULTS: A total of 240 recruits were randomized (1:1) into the ASICA (n=121, 50.4%) or control (n=119, 49.6%) groups. There were no significant differences between groups for melanoma worry at 12 months (mean difference: 0.12, 95% CI -0.6 to 0.84; P=.74), 3 months (0.23, 95% CI -0.31 to 0.78; P=.40), or 6 months (-0.1, 95% CI -0.7 to 0.51; P=.76). The ASICA group had lower anxiety scores at 12 months (-0.54, 95% CI -1.31 to 0.230; P=.17), 3 months (-0.13, 95% CI -0.79 to 0.54; P=.71), and significantly at 6 months (-1.00, 95% CI -1.74 to -0.26; P=.009). Depression scores were similar, being lower at 12 months (-0.44, 95% CI -1.11 to 0.23; P=.20) and 3 months (-0.24, 95% CI -0.84 to 0.35; P=.42) but only significantly lower at 6 months (-0.77, 95% CI -1.41 to -0.12; P=.02). The ASICA group had significantly higher quality of life scores at 12 months (0.044, 95% CI 0.003-0.085; P=.04) and 6 months (0.070, 95% CI 0.032-0.107; P<.001) and nonsignificantly at 3 months (0.024, 95% CI -0.006 to 0.054; P=.11). ASICA users reported significantly more regular (>5) TSSEs during the study year and significantly higher levels of self-efficacy in conducting TSSE. They also reported significantly higher levels of planning and intention to perform TSSE in the future.
CONCLUSIONS: Using ASICA for 12 months does not increase melanoma worry, can reduce anxiety and depression, and may improve quality of life. ASICA has the potential to improve the well-being and vigilance of survivors of melanoma and enable the benefits of regular TSSE.
TRIAL REGISTRATION: ClinicalTrials.gov NCT03328247; https://clinicaltrials.gov/ct2/show/NCT03328247.
INTERNATIONAL REGISTERED REPORT IDENTIFIER (IRRID): RR2-10.1186/s13063-019-3453-x.

Keywords

Associated Data

ClinicalTrials.gov | NCT03328247

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Grants

  1. 21685/Cancer Research UK
  2. HSRU1/Chief Scientist Office

Word Cloud

Created with Highcharts 10.0.00months-095%CIP=melanomaASICA12TSSE6significantlyprimary3-1well-beingrandomizedqualitylifeMelanomasurvivorsAchievingSelf-directedIntegratedCancerAftercarecareworryanxietylowerscoreshighertotalTSSEsstudypsychologicalpracticeself-directedinterventionusualfirstIICcutaneoustrialincreaseusersoutcomesScaledepressionDepressiongroups84742331group5411reportedregularlevelsimproveBACKGROUND:commonincreasingincidenceGuidelinesrecommendmonthlyskinself-examinationsdetectrecurrentnewmelanomasunderperformeddespiteevidencebenefitOBJECTIVE:compareseffectdigitaltreatmentpatientstreatedstagewithinpreceding60METHODS:clinicalconducted2UKNationalHealthServicehospitalsAberdeenRoyalInfirmaryGrampianAddenbrooke'sCambridgeAdults≥18yearsdiagnosedreceivetablet-basedpromptingsupportinghypothesisaffectedcomparedcontrolswithoutaffectingmainWorryHospitalAnxietyEQ-5D-5LwellsecondarycollectedusingpostalquestionnairesfollowingrandomizationRESULTS:240recruits1:1n=121504%controln=119496%significantdifferencesmeandifference:7840175176230171379710026009similar4420243542774102044003-008504070032-0107P<001nonsignificantly024006054>5yearself-efficacyconductingalsoplanningintentionperformfutureCONCLUSIONS:UsingcanreducemaypotentialvigilanceenablebenefitsTRIALREGISTRATION:ClinicalTrialsgovNCT03328247https://clinicaltrialsgov/ct2/show/NCT03328247INTERNATIONALREGISTEREDREPORTIDENTIFIERIRRID:RR2-101186/s13063-019-3453-xInterventionDetectionRecurrentSecondPrimarySurvivorsMelanoma:PilotRandomizedControlledTrialcancereHealthmobilephonecontrolledsurvivorship

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