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Randomized Controlled Trial
. 2011;16(11):1649-57.
doi: 10.1634/theoncologist.2011-0133. Epub 2011 Sep 26.

Physical exercise for cancer patients with advanced disease: a randomized controlled trial

Affiliations
Randomized Controlled Trial

Physical exercise for cancer patients with advanced disease: a randomized controlled trial

Line M Oldervoll et al. Oncologist. 2011.

Abstract

Background: Physical exercise can improve cancer patients' functioning and reduce their symptom levels. A randomized, controlled trial was launched to test the hypothesis that physical exercise reduces fatigue and improves physical performance in cancer patients with advanced and incurable disease.

Methods: Cancer patients (n = 231) with a life expectancy ≤2 years were randomized to a physical exercise group (PEG, n = 121) or a control usual care group (UCG, n = 110). The PEG exercised under supervision 60 minutes twice a week for 8 weeks. Assessments were performed before and after the intervention. The primary outcome was physical fatigue (PF) measured by the Fatigue Questionnaire. Physical performance was a secondary outcome measured by the Shuttle Walk Test (SWT) and hand grip strength (HGS) test. Analyses were performed after multiple imputations for missing data. The trial is registered with ClinicalTrials.gov (identifier, NCT00397774).

Findings: Thirty-six percent of the PEG were lost to follow-up compared with 23% of the UCG, primarily as a result of disease progression. Seventy-eight PEG and 85 UCG patients completed the intervention. Analyses showed no significant between-group effects in PF. However, clinically and statistically significant between-group effects were found for the SWT and HGS test.

Interpretation: Fatigue was not reduced but physical performance (SWT and HGS test) was significantly improved after 8 weeks of physical exercise. Physical exercise might therefore be a suitable approach for maintaining physical capacity in cancer patients with incurable and advanced disease.

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Conflict of interest statement

Disclosures: Line M. Oldervoll: None; Jon H. Loge: None; Stian Lydersen: None; Hanna Paltiel: None; May B. Asp: None; Unni V. Nygaard: None; Elisabeth Oredalen: None; Tone L. Frantzen: None; Ingvild Lesteberg: None; Lise Amundsen: None; Marianne J. Hjermstad: None; Dagny F. Haugen: None; Ørnulf Paulsen: None; Stein Kaasa: None.

Section editors Eduardo Bruera: None; Russell K. Portenoy: Cephalon, CNS Bio, Grupo Ferrer, Purdue Pharma, Xenon (financial relationships); Ameritox, Archimedes Pharmaceuticals, Cephalon, Covidien Mallinckrodt Inc., Endo Pharmaceuticals, Forest Labs, Meda Pharmaceuticals, Ortho-McNeil Janssen Scientific Affairs LLD, Otsuka Pharma, Purdue Pharma, Tempur-Pedic Corporation (RF).

Reviewer “A”: None.

Reviewer “B”: Boehringer Ingelheim, KangLaiTe USA (C/A).

Figures

Figure 1.
Figure 1.
Patient flowchart showing numbers of patients eligible, refused to participate, recruited, randomized, lost to follow-up, and completed.

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