A multi-modal intervention for managing the fatigue-sleep disturbance-depressed mood symptom cluster in breast cancer patients undergoing chemotherapy: A pilot study
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 inte...
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Elsevier,
2023-08-01T00:00:00Z.
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LEADER | 00000 am a22000003u 4500 | ||
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001 | doaj_b61b48c6f81c46e69327114c51bed4a8 | ||
042 | |a dc | ||
100 | 1 | 0 | |a Wai Man Wong |e author |
700 | 1 | 0 | |a Dorothy N.S. Chan |e author |
700 | 1 | 0 | |a Kai Chow Choi |e author |
700 | 1 | 0 | |a Yin Ping Choy |e author |
700 | 1 | 0 | |a Winnie K.W. So |e author |
245 | 0 | 0 | |a A multi-modal intervention for managing the fatigue-sleep disturbance-depressed mood symptom cluster in breast cancer patients undergoing chemotherapy: A pilot study |
260 | |b Elsevier, |c 2023-08-01T00:00:00Z. | ||
500 | |a 2347-5625 | ||
500 | |a 10.1016/j.apjon.2023.100269 | ||
520 | |a 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). | ||
546 | |a EN | ||
690 | |a Symptom cluster | ||
690 | |a Symptom management | ||
690 | |a Breast cancer | ||
690 | |a Cancer-related fatigue | ||
690 | |a Sleep disturbance | ||
690 | |a Depressed mood | ||
690 | |a Neoplasms. Tumors. Oncology. Including cancer and carcinogens | ||
690 | |a RC254-282 | ||
690 | |a Nursing | ||
690 | |a RT1-120 | ||
655 | 7 | |a article |2 local | |
786 | 0 | |n Asia-Pacific Journal of Oncology Nursing, Vol 10, Iss 8, Pp 100269- (2023) | |
787 | 0 | |n http://www.sciencedirect.com/science/article/pii/S2347562523000872 | |
787 | 0 | |n https://doaj.org/toc/2347-5625 | |
856 | 4 | 1 | |u https://doaj.org/article/b61b48c6f81c46e69327114c51bed4a8 |z Connect to this object online. |