Aerobic Exercise And Cancer-Related Fatigue In Adults

作者
George A. Kelley,Kristi S. Kelley
出处
期刊:Medicine and Science in Sports and Exercise [Lippincott Williams & Wilkins]
卷期号:49 (5S): 590-590
标识
DOI:10.1249/01.mss.0000518541.14402.03
摘要

BACKGROUND: Using the traditional random-effects model, a recent meta-analysis of randomized controlled trials reported a statistically significant standardized mean difference (SMD) reduction in cancer-related fatigue (CRF) as a result of aerobic exercise (SMD, -0.22, 95% CI, -0.39 to -0.04, p = 0.01). However, a recently developed inverse heterogeneity (IVhet) model has been shown to be more valid than the traditional random-effects model. PURPOSE: The purpose of this study was to compare these previous meta-analytic results with those using the IVhet model. METHODS: Using data from a previous meta-analysis that included 36 SMD effect sizes (ES’s) representing 2,830 adults (1,426 exercise, 1,404 control), results were pooled using the IVhet model. In addition, absolute and relative differences between the IVhet and random-effects results for CRF were calculated as well as influence analysis with each SMD ES deleted from the IVhet model once. Non-overlapping 95% confidence intervals were considered statistically significant. RESULTS: A statistically non-significant reduction in CRF fatigue was found as a result of aerobic exercise using the IVhet model (SMD, -0.08, 95% CI, -0.31 to 0.14, p = 0.46). The IVhet model yielded a SMD ES that was 0.14 (63.6%) smaller than the random-effects model. With each study deleted from the IVhet model once, results remained statistically non-significant with SMD ES’s ranging from -0.11 (95% CI, -0.33 to 0.11) to -0.06 (95% CI, -0.28 to 0.16). CONCLUSIONS: The results of the current study suggest that there is currently insufficient evidence to support the use of aerobic exercise for reducing CRF in adults. Future studies should consider use of the IVhet versus traditional random-effects model when conducting aggregate data meta-analyses. Supported by NIH Grant U54GM104942

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