1. Effect of Baduanjin exercise intervention on cognitive function and quality of life in women with breast cancer receiving chemotherapy: study protocol of a randomized controlled trial.
- Author
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Wei, Xiao-Lin, Yuan, Ru-Zhen, Jin, Yong-Mei, Li, Shu, Wang, Ming-Yue, Jiang, Jie-Ting, Wu, Cai-Qin, and Li, Kun-Peng
- Subjects
COGNITIVE ability ,CANCER chemotherapy ,ANXIETY ,BREAST cancer ,RESEARCH protocols ,QUALITY of life ,CANCER fatigue ,CLINICAL trial registries - Abstract
Background: More than 50% cognitive impairment was reported by cancer patients before and after medical treatment. However, there are no effective interventions to manage the cognitive problem in women with breast cancer. This pilot study was designed to evaluate the protective effect of Baduanjin exercise on cognitive function and cancer-related symptoms in women with early-stage breast cancer undergoing chemotherapy. Method: A single-blinded, randomized control trial was designed. The trial will recruit 70 patients with early-stage breast cancer scheduled to receive chemotherapy from Shanghai in China. All participants will be randomly assigned to (1:1) the supervised Baduanjin group (5 times/week, 30 min each time) or the wait-list control group for 3 months. The effect of Baduanjin exercise intervention will be evaluated by outcome measures including subjective and objective cognitive function, symptoms (fatigue, depression, and anxiety), and health-related quality of life at pre-intervention (T0), 8 weeks (T1), and 12 weeks (T2). The PCI score in the FACT-Cog as the primary cognitive outcome will be reported descriptively, while effect sizes and 95% confidence intervals (CIs) will be calculated. The collected data will be analyzed by using an intention-to-treat principle and linear mixed-effects modeling. Discussion: This is the first randomized clinical trial to investigate whether Baduanjin exercise will have a positive role in improving cognitive function in women with breast cancer receiving chemotherapy. If possible, Baduanjin exercise will be a potential non-pharmacological intervention to manage cognitive dysfunction and promote survivorship care among breast cancer survivors. Trial registration: Chinese Clinical Trial Registry (ChiCTR) ChiCTR2000033152. Registered on 22 May 2020 [ABSTRACT FROM AUTHOR]
- Published
- 2021
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