Comparative Effectiveness of Cheonwangbosimdan (Tian Wang Bu Xin Dan) Versus Cognitive-Behavioral Therapy for Insomnia in Cancer Patients: A Randomized, Controlled, Open-Label, Parallel-Group, Pilot Trial

被引:9
作者
Moon, Sun-Young [1 ,2 ]
Jerng, Ui Min [3 ]
Kwon, O-Jin [1 ]
Jung, So-Young [1 ]
Lee, Jee Young [4 ,5 ]
Yoon, Seong Woo [4 ,5 ]
Shin, Won-Chul [4 ]
Byun, Jung-Ick [4 ]
Lee, Jun-Hwan [1 ,2 ]
机构
[1] Korea Inst Oriental Med, 1672 Yuseongdae Ro, Daejeon 34054, South Korea
[2] Univ Sci & Technol UST, Campus Korea Inst Oriental Med, Daejeon, South Korea
[3] Sang Ji Univ, Korean Med Hosp, Wonju, South Korea
[4] Kyung Hee Univ Hosp Gangdong, Seoul, South Korea
[5] Kyung Hee Univ, Seoul, South Korea
关键词
insomnia; cancer-related insomnia; Korean medicine; Cheonwangbosim liquid; cognitive-behavioral therapy; comparative effectiveness; QUALITY-OF-LIFE; SLEEP DISTURBANCE; COLORECTAL-CANCER; DEPRESSED MOOD; KOREAN VERSION; FATIGUE; RISK; SYMPTOMS; DURATION; PRESCRIPTIONS;
D O I
10.1177/1534735420935643
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Cancer patients have a 2 times higher prevalence of insomnia than healthy populations and cancer-related insomnia has received minimal attention while insomnia can aggravate the rehabilitation of cancer patients. Cheonwangbosimdan is a Korean herbal medicine generally used to relieve sleep deprivation, however, few studies presented the effects of Cheonwangbosimdan on cancer-related insomnia. The purpose of study is to examine the feasibility of Cheonwangbosimdan treatments for cancer patients. Twenty-two participants were allocated into a Cheonwangbosimdan or cognitive-behavioral therapy for insomnia (CBT-I) control group by equal number. The intervention group took Cheonwangbosimdan liquid once in a day and attend visits once a week for 4 weeks. The CBT-I group underwent individualized behavioral therapy 4 times in 4 weeks. The primary outcome is changes in the Insomnia Severity Index (ISI) from baseline to the end of the trial. Responses to the Pittsburgh Sleep Quality Index (PSQI), Epworth Sleepiness Scale (ESS), Zung Self-Rating Anxiety Scale (SAS), Brief Fatigue Inventory (BFI), Euroqol-5 Dimensions-5 Levels (EQ-5D-5L), and Eastern Cooperative Oncology Group Performance Status (ECOG-PS) were secondary outcomes used to evaluate the quality of sleep. Outcomes were measured at a follow-up visit (visit 5) in the fifth week of the trial. There is no difference between 2 groups, but both groups showed tendency to alleviate cancer insomnia symptoms. SAS-K showed significant difference between the 2 groups (P < .001), as treatment group score was highly lowered than control group score. The study can contribute to more attentive care for insomnia in cancer patients.
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页数:12
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