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Individualized Acupuncture for Symptom Relief in Functional Dyspepsia: A Randomized Controlled Trial

Authors
Ko, Seok-JaeKuo, BradenKim, Seul-KiLee, HyangsookKim, JinsungHan, GajinKim, JuyeonKim, Song-YiJang, SeungwonSon, JiyoungKim, MinjiLee, HyejungYeo, InkwonJoo, Kwang RoPark, Jae-Woo
Issue Date
Dec-2016
Publisher
MARY ANN LIEBERT, INC
Keywords
acupuncture; alternative therapy; CAM
Citation
JOURNAL OF ALTERNATIVE AND COMPLEMENTARY MEDICINE, v.22, no.12, pp 997 - 1006
Pages
10
Journal Title
JOURNAL OF ALTERNATIVE AND COMPLEMENTARY MEDICINE
Volume
22
Number
12
Start Page
997
End Page
1006
URI
https://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/9329
DOI
10.1089/acm.2016.0208
ISSN
1075-5535
1557-7708
Abstract
Objectives: This study was implemented to evaluate the effect of individualized acupuncture treatment (AT) on functional dyspepsia (FD). Methods: A randomized, waitlist-controlled, two-center trial was performed. Seventy-six patients with FD were enrolled in the trial with partially individualized AT in a more realistic clinical setting performed twice a week for 15 minutes a session over 4 weeks. The participants were randomly allocated to a group receiving 8 sessions of AT for 4 weeks or a waitlist control group. After 4 consecutive weeks, the AT group was followed up without AT and the control group received the identical AT. The proportion of responders with adequate symptom relief, Nepean Dyspepsia Index (NDI), FD-related quality of life, Beck Depression Inventory, State-Trait Anxiety Inventory, Acupuncture Belief Scale, and acupuncture credibility test were assessed. Results: After the first 4 weeks, the proportion of responders significantly improved (59% in AT group [n = 37] versus 3% in control group [n = 39]; p < 0.001). The difference was no longer significant at 8 weeks, at which point the waitlist control group showed similar improvement after receiving AT (68% in the AT group versus 79% in the control group). Total NDI scores were significantly reduced in the AT group compared with the waitlist group (p = 0.03). Among NDI items, discomfort (p = 0.01), burning (p = 0.02), fullness after eating (p = 0.02), and burping (p = 0.02) were significantly improved in the AT group compared with the control group. No significant differences were observed between groups in other secondary variables. Conclusion: Individualized AT adequately relieves symptoms in patients with FD, and this effect may persist up to 8 weeks.
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