Author: Liu L1, Petrich S2, McLaren B3, Kelly L3, Baxter GD4
Affiliation: <sup>1</sup>Centre for Health, Activity and Rehabilitation Research, School of Physiotherapy, University of Otago, Dunedin 9054, New Zealand. Electronic address: lizhou.liu@otago.ac.nz.
<sup>2</sup>Department of Surgical Sciences, Southern District Health Board, Dunedin 9016, New Zealand.
<sup>3</sup>Oncology Department, Southern District Health Board, Dunedin 9016, New Zealand.
<sup>4</sup>Centre for Health, Activity and Rehabilitation Research, School of Physiotherapy, University of Otago, Dunedin 9054, New Zealand.
Conference/Journal: J Integr Med.
Date published: 2018 Mar
Other:
Volume ID: 16 , Issue ID: 2 , Pages: 99-105 , Special Notes: doi: 10.1016/j.joim.2017.12.011. Epub 2018 Jan 31. , Word Count: 306
BACKGROUND: Breast cancer patients experience various side effects during cancer therapy, often resulting in reduced quality of life and poor adherence to treatment. A limited range of proven interventions has been developed to target such side effects. While Tai Chi offers benefits for the health and well-being of breast cancer survivors, the effectiveness of Tai Chi across the treatment continuum has not been evaluated. Improved patient education and support has been suggested as a priority for breast cancer care. This pilot study assesses the feasibility of a randomized controlled trial (RCT) to evaluate the effectiveness of "an integrative Tai Chi" (ANITA) program for breast cancer patients undergoing cancer therapy.
METHODS/DESIGN: This is a single-centre, two-arm feasibility RCT. Twenty-four patients with breast cancer who have undergone surgical treatment will be recruited from the Dunedin Hospital (New Zealand) over a 12-month period (from August 2017 to July 2018). Subject to informed consent, patients will be randomized to receive standard cancer treatment alone or standard cancer treatment plus the ANITA program, consisting of peer support, health education, and Tai Chi Ruler exercise. The program runs alongside the patient's adjuvant cancer therapy, which may include chemotherapy, radiation therapy, antibody treatment, and/or antihormonal therapy. Analysis in this study will focus on process evaluation of participant recruitment, retention, treatment fidelity, acceptability of the program, and occurrence of adverse events. Clinical outcomes (i.e., fatigue, sleep quality, anxiety and depression and quality of life) will be assessed at baseline, and at 12 weeks and 24 weeks post-randomization.
DISCUSSION: Outcomes from this study will inform the feasibility and methodology for a future fully-powered RCT.
TRIAL REGISTRATION: Australian New Zealand Clinical Trials Registry with the identifier ACTRN12617000975392.
Copyright © 2018 Shanghai Changhai Hospital. Published by Elsevier B.V. All rights reserved.
KEYWORDS: Breast cancer; Feasibility study; Health education; Peer support; Randomized controlled trial; Tai Chi
PMID: 29526243 DOI: 10.1016/j.joim.2017.12.011