i-Move, a personalised exercise intervention for patients with advanced melanoma receiving immunotherapy: a randomised feasibility trial protocol.
Adolescent
Adult
Aged
Aged, 80 and over
Antineoplastic Agents, Immunological
/ adverse effects
Clinical Protocols
Exercise Therapy
/ methods
Fatigue
/ chemically induced
Feasibility Studies
Female
Follow-Up Studies
Humans
Immunotherapy
/ adverse effects
Male
Melanoma
/ drug therapy
Middle Aged
Patient Acceptance of Health Care
Patient Compliance
Patient Reported Outcome Measures
Pilot Projects
Skin Neoplasms
/ drug therapy
Treatment Outcome
Young Adult
adverse events
exercise
immune checkpoint inhibitors
immunotherapy
treatment-related fatigue
Journal
BMJ open
ISSN: 2044-6055
Titre abrégé: BMJ Open
Pays: England
ID NLM: 101552874
Informations de publication
Date de publication:
28 02 2020
28 02 2020
Historique:
entrez:
2
3
2020
pubmed:
3
3
2020
medline:
16
2
2021
Statut:
epublish
Résumé
There is increasing evidence demonstrating the benefits of exercise in counteracting cancer treatment-related fatigue. Immunotherapy is an established treatment for advanced melanoma, and is associated with fatigue in a third of patients. The safety and efficacy of exercise in counteracting treatment-related fatigue in patients with advanced melanoma receiving immunotherapy are yet to be determined. This study aims to assess the safety, adherence to and acceptability of a mixed-methods parallel-group, pilot randomised controlled trial of a personalised, 12-week semi-supervised exercise programme prescribed by an exercise physiologist (iMove) in 30 patients with stage IV melanoma scheduled to commence immunotherapy: single agent ipilimumab, nivolumab or pembrolizumab, or combination ipilimumab and nivolumab. The trial will be used to provide preliminary evidence of the potential efficacy of exercise for managing fatigue. Thirty participants will be recruited from a specialist cancer centre between May and September, 2019. Participants will be randomised 1:1 to receive iMove, or usual care (an information booklet about exercise for people with cancer). Feasibility data comprise: eligibility; recruitment and retention rates; adherence to and acceptability of exercise consultations, personalised exercise programme and study measures; and exercise-related adverse events. Patient-reported outcome measures assess potential impact of the exercise intervention on: fatigue, role functioning, symptoms and quality of life. Follow-up will comprise five time points over 24 weeks. Physical assessments measure physical fitness and functioning. This study was reviewed and approved by the Peter MacCallum Cancer Centre Human Research Ethics Committee (HREC/48927/PMCC-2019). The findings from this trial will be disseminated via conference presentations and publications in peer-reviewed journals, and by engagement with clinicians, media, government and consumers. In particular, we will promote the outcomes of this work among the oncology community should this pilot indicate benefit for patients. ACTRN12619000952145; Pre-results.
Identifiants
pubmed: 32114479
pii: bmjopen-2019-036059
doi: 10.1136/bmjopen-2019-036059
pmc: PMC7050356
doi:
Substances chimiques
Antineoplastic Agents, Immunological
0
Banques de données
ANZCTR
['ACTRN12619000952145']
Types de publication
Journal Article
Randomized Controlled Trial
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
e036059Informations de copyright
© Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.
Déclaration de conflit d'intérêts
Competing interests: None declared.
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