High-intensity aerobic interval training and resistance training are feasible in rectal cancer patients undergoing chemoradiotherapy: a feasibility randomized controlled study.

exercise high-intensity interval training neoadjuvant chemoradiotherapy rectal cancer resistance training

Journal

Reports of practical oncology and radiotherapy : journal of Greatpoland Cancer Center in Poznan and Polish Society of Radiation Oncology
ISSN: 1507-1367
Titre abrégé: Rep Pract Oncol Radiother
Pays: Poland
ID NLM: 100885761

Informations de publication

Date de publication:
2022
Historique:
received: 01 02 2022
accepted: 23 02 2022
entrez: 27 10 2022
pubmed: 28 10 2022
medline: 28 10 2022
Statut: epublish

Résumé

There has been growing evidence of the benefits of high-intensity aerobic interval training (HIIT) and resistance training (RES) for populations with cancer. However, these two modalities have not yet been performed alone in rectal cancer patients undergoing neoadjuvant chemoradiotherapy (NACR T). Therefore, this study aimed to determine the feasibility of HIIT and RES in rectal cancer patients undergoing NACR T. Rectal cancer patients set to undergo NACRT were randomly assigned to HIIT intervention, RES intervention, or the usual care. Feasibility of HIIT and RES was assessed by measuring recruitment rate, adherence (retention rate, attendance rate, and exercise sessions duration and intensity), and adverse events. Endpoints (changes in fatigue, health-related quality of life, depression, daytime sleepiness, insomnia, sleep quality, functional exercise capacity, and executive function) were assessed at baseline and at week 5. Among the 20 eligible patients, 18 subjects were enrolled and completed the study, yielding a 90% recruitment rate and 100% retention rate. Attendance at exercise sessions was excellent, with 92% in HIIT and 88% in RES. No exercise-related adverse events occurred. This study demonstrated that HIIT and RES are feasible in rectal cancer patients undergoing NACR T. www.clinicaltrials.gov, NCT03252821 (date of registration: March 30, 2017).

Sections du résumé

Background UNASSIGNED
There has been growing evidence of the benefits of high-intensity aerobic interval training (HIIT) and resistance training (RES) for populations with cancer. However, these two modalities have not yet been performed alone in rectal cancer patients undergoing neoadjuvant chemoradiotherapy (NACR T). Therefore, this study aimed to determine the feasibility of HIIT and RES in rectal cancer patients undergoing NACR T.
Materials and methods UNASSIGNED
Rectal cancer patients set to undergo NACRT were randomly assigned to HIIT intervention, RES intervention, or the usual care. Feasibility of HIIT and RES was assessed by measuring recruitment rate, adherence (retention rate, attendance rate, and exercise sessions duration and intensity), and adverse events. Endpoints (changes in fatigue, health-related quality of life, depression, daytime sleepiness, insomnia, sleep quality, functional exercise capacity, and executive function) were assessed at baseline and at week 5.
Results UNASSIGNED
Among the 20 eligible patients, 18 subjects were enrolled and completed the study, yielding a 90% recruitment rate and 100% retention rate. Attendance at exercise sessions was excellent, with 92% in HIIT and 88% in RES. No exercise-related adverse events occurred.
Conclusion UNASSIGNED
This study demonstrated that HIIT and RES are feasible in rectal cancer patients undergoing NACR T.
Trial registration UNASSIGNED
www.clinicaltrials.gov, NCT03252821 (date of registration: March 30, 2017).

Identifiants

pubmed: 36299392
doi: 10.5603/RPOR.a2022.0036
pii: rpor-27-2-198
pmc: PMC9591035
doi:

Banques de données

ClinicalTrials.gov
['NCT03252821']

Types de publication

Journal Article

Langues

eng

Pagination

198-208

Informations de copyright

© 2022 Greater Poland Cancer Centre.

Déclaration de conflit d'intérêts

Conflict of interest None declared.

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Auteurs

Elise Piraux (E)

Pôle de Neuro Musculo Skeletal Lab, Pôle de Pneumologie, ORL and Dermatologie, Institut de Recherche Expérimentale et Clinique, Clinical Neuroscience, Institute of Neurosciences, Université Catholique de Louvain, Haute Ecole Léonard de Vinci, PARNASSE-ISEI, Secteur de Kinésithérapie, Cliniques Universitaires Saint-Luc, Brussels, Belgium.

Gregory Reychler (G)

Pôle de Pneumologie, ORL and Dermatologie, Institut de Recherche Expérimentale et Clinique, Université Catholique de Louvain, Haute Ecole Léonard de Vinci, PARNASSE-ISEI, Secteur de Kinésithérapie, Service de Pneumologie, Cliniques Universitaires Saint-Luc, Brussels, Belgium.

David Vancraeynest (D)

Pôle de Recherche Cardiovasculaire, Institut de Recherche Expérimentale et Clinique, Université Catholique de Louvain, Service de Cardiologie, Cliniques Universitaires Saint-Luc, Brussels, Belgium.

Xavier Geets (X)

Molecular Imaging, Radiotherapy and Oncology, Institut de Recherche Expérimentale et Clinique, Université Catholique de Louvain, Service de Radiothérapie Oncologique, Cliniques universitaires Saint-Luc, Brussels, Belgium.

Daniel Léonard (D)

Service de Chirurgie et Transplantation Abdominale, Unité de Chirurgie Colorectale, Cliniques Universitaires Saint-Luc, Brussels, Belgium.

Gilles Caty (G)

Clinical Neuroscience, Institute of Neurosciences, Université Catholique de Louvain, Service de Médecine Physique et Réadaptation, Cliniques Universitaires Saint-Luc,Brussels, Belgium.

Classifications MeSH