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Published on: May 31, 2016
A multi-modal intervention for managing the fatigue-sleep disturbance-depressed mood symptom cluster in breast cancer
Wai Man Wong1,2, Dorothy N S Chan1, Kai Chow Choi1
1The Nethersole School of Nursing, The Chinese University of Hong Kong, Hong Kong SAR, China.
Objective:
To examine the feasibility and acceptability of a multi-modal intervention for managing the cancer-related fatigue-sleep disturbance-depressed mood (F-S-D) symptom cluster in patients with breast cancer (BC) and receiving chemotherapy in Hong Kong, and the preliminary effects of such intervention on the occurrence of the F-S-D symptom cluster in these patients.
Methods:
This study was a single-blind randomized controlled trial. Patients with BC scheduled for chemotherapy were recruited. Intervention participants received a weekly nurse-led multi-modal intervention lasting 7 weeks. The feasibility parameters and adverse events were assessed using logbook records. Acceptability was evaluated using a program evaluation questionnaire. F-S-D symptoms and quality of life (QOL) were measured at baseline (T0), upon intervention completion (T1), and 3 months after intervention completion (T2). Generalized estimating equation analyses were used.
Results:
Fifty participants were enrolled. The eligibility and enrollment rates were 11% and 87.7%, respectively. The rate of adherence to the intervention was 96%. No adverse events were reported. All participants were satisfied with the intervention, which had significant effects in terms of reducing the occurrence of the F-S-D symptom cluster at T2 (P = 0.035) and improving QOL at T1 and T2 (T1: P = 0.035; T2: P = 0.012).
Conclusions:
The multi-modal intervention is a feasible, acceptable, and safe intervention that demonstrated preliminary positive effects in managing the F-S-D symptom cluster and improving QOL in patients with BC and receiving chemotherapy in Hong Kong. This study provides key insights into F-S-D symptom cluster management in patients with BC.
Trial Registration:
ChiCTR2100047819 (Chinese Clinical Trial Register).
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