Feasibility, usability and acceptance of weekly electronic patient-reported outcomes among patients receiving pelvic CT- or online MR-guided radiotherapy - A prospective pilot study.

AE, Adverse event Acceptance CTCAE, Common Terminology Criteria of Adverse Events ECOG, Eastern Cooperative Oncology Group EORTC, European Organization for Research and Treatment of Cancer Feasibility Gy, Gray MR, Magnetic resonance MRgRT, Magnetic resonance guided radiotherapy NCI, National Cancer Institute Online MRgRT PRO, Patient-Reported Outcome PRO-CTCAE, Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Patient-reported outcome (PRO) QLQ-C30, EORTC general core module QoL, Quality of life RT, Radiotherapy Radiotherapy Usability WHO, World Health Organization Performance Status ePRO, Electronic Patient-Reported Outcome

Journal

Technical innovations & patient support in radiation oncology
ISSN: 2405-6324
Titre abrégé: Tech Innov Patient Support Radiat Oncol
Pays: England
ID NLM: 101762366

Informations de publication

Date de publication:
Mar 2022
Historique:
received: 21 09 2021
revised: 11 11 2021
accepted: 06 12 2021
entrez: 3 1 2022
pubmed: 4 1 2022
medline: 4 1 2022
Statut: epublish

Résumé

The potential of patient symptoms being monitored longitudinally in radiotherapy (RT) is still unexploited. When novel technologies like online adaptive MR-guided radiotherapy (MRgRT) are evaluated, weekly electronic patient-reported outcomes (ePROs) may add knowledge about the symptom trajectory. This study aimed at evaluating feasibility, usability and acceptance of weekly ePRO among patients receiving pelvic radiotherapy. In a mixed-methods convergent design, a prospective pilot study enrolled patients referred to pelvic radiotherapy with curative intent. Patients used their own device at home to self-report PRO weekly during and four weeks following radiotherapy and week 8, 12, and 24 (paper-questionnaire as an alternative). Feasibility was extracted from the ePRO software. The Patient Feedback Form and patient interviews were used to explore usability and patient acceptance. Patients were informed that clinicians had no access to PRO responses. In total, 40 patients were included; 32 patients with prostate cancer and 8 with cervical cancer (consent rate 87%), median age 68 (36-76). The majority did digital reporting (93%). 85% of patients responded to ≥80% of the weekly questionnaires with 91% average adherence to weekly completion (60% for follow-up), although lower for patients ≥age 70. Time spent on ePRO (97%) and frequency of reporting (92%) was considered appropriate. Interviews (n = 14) revealed the application was usable and the patients requested real-time feedback from the clinicians. Recruitment for ePRO during radiotherapy was feasible and adherence to weekly self-reporting high. The digital application was usable and weekly frequency and time spent acceptable. Real-time feedback from the clinicians is requested by the patients.

Identifiants

pubmed: 34977367
doi: 10.1016/j.tipsro.2021.12.001
pii: S2405-6324(21)00044-5
pmc: PMC8686059
doi:

Types de publication

Journal Article

Langues

eng

Pagination

8-15

Informations de copyright

© 2021 The Authors. Published by Elsevier B.V. on behalf of European Society for Radiotherapy & Oncology.

Déclaration de conflit d'intérêts

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

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Auteurs

P K Møller (PK)

Department of Oncology, AgeCare, Academy of Geriatric Cancer Research, Odense University Hospital, Denmark.
Department of Clinical Research, University of Southern Denmark, Denmark.

H Pappot (H)

Department of Oncology, Rigshospitalet, University Hospital of Copenhagen and Department of Clinical Medicine, University of Copenhagen, Denmark.

U Bernchou (U)

Department of Clinical Research, University of Southern Denmark, Denmark.
Laboratory of Radiation Physics, Odense University Hospital, Denmark.

T Schytte (T)

Department of Oncology, Odense University Hospital, Denmark.
Department of Clinical Research, University of Southern Denmark, Denmark.

Z V Mortensen (ZV)

Department of Oncology, Odense University Hospital, Denmark.

M F Á Brúnni (MFÁ)

Department of Oncology, Odense University Hospital, Denmark.

K B Dieperink (KB)

Department of Oncology, AgeCare, Academy of Geriatric Cancer Research, Odense University Hospital, Denmark.
Department of Clinical Research, University of Southern Denmark, Denmark.

Classifications MeSH