Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/103906
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dc.contributorDepartment of Rehabilitation Sciences-
dc.creatorPang, JCYen_US
dc.creatorFu, ASNen_US
dc.creatorLam, SKHen_US
dc.creatorPeng, Ben_US
dc.creatorFu, ACLen_US
dc.date.accessioned2024-01-10T02:41:21Z-
dc.date.available2024-01-10T02:41:21Z-
dc.identifier.urihttp://hdl.handle.net/10397/103906-
dc.language.isoenen_US
dc.publisherPublic Library of Scienceen_US
dc.rights© 2022 Pang et al. This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.en_US
dc.rightsThe following publication Pang, J. C., Fu, A. S., Lam, S. K., Peng, B., & Fu, A. C. (2022). Ultrasound-guided dry needling versus traditional dry needling for patients with knee osteoarthritis: A double-blind randomized controlled trial. Plos one, 17(9), e0274990 is available at https://doi.org/10.1371/journal.pone.0274990.en_US
dc.titleUltrasound-guided dry needling versus traditional dry needling for patients with knee osteoarthritis : a double-blind randomized controlled trialen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.volume17en_US
dc.identifier.issue9en_US
dc.identifier.doi10.1371/journal.pone.0274990en_US
dcterms.abstractObjective-
dcterms.abstractTo compare the effect of ultrasound (US)-guided dry needling (DN) with traditional DN in the treatment of pain and dysfunction for patients with knee osteoarthritis (KOA).-
dcterms.abstractDesign-
dcterms.abstractA double-blind, randomized controlled trial.-
dcterms.abstractMethods-
dcterms.abstractPatients (25 male and 65 female), age 50-80 years diagnosed with KOA were recruited and randomly assigned to one of three groups in a 1:1:1 ratio for intervention: real US-guided DN with exercise therapy (G1), placebo US-guided DN with exercise therapy (G2), and exercise therapy solely (G3). G1 and G2 were blinded to the application of real or placebo US guidance by turning the monitor of US imaging out-of-view from participants' vantage points. The effectiveness of blinding was evaluated by asking the participants whether they had received real-US guided DN. The responses were assessed by Chi-square test. Visual Analogue Scale (VAS), Knee injury, and Osteoarthritis Outcome Score (KOOS) subscales (KOOS-pain, KOOS-symptoms, KOOS-quality-of-life (QoL)) were collected at baseline, 4 weeks, and 8 weeks by a blinded assessor. Data were analyzed by mixed model analysis of variance (ANOVA) with Bonferroni correction.-
dcterms.abstractResults-
dcterms.abstractEighty-four participants (61.26 +/- 5.57 years) completed the study. G1 achieved significant improvement in VAS at 8 weeks compared to G2 and G3 (G1 vs. G2: MD = -15.61, 95% CI [-25.49, -5.51], p = 0.001; G1 vs. G3: MD = -19.90, 95% CI [-29.71, -10.08], p<0.001). G1 achieved significant improvement in KOOS-pain at 8 weeks compared to G2 and G3 (G1 vs. G2: MD = 9.76, 95% CI [2.38, 17.14], p = 0.006; G1 vs. G3: MD = 9.48, 95% CI [2.31, 16.66], p = 0.010). KOOS-symptoms and KOOS-QoL were not statistically significant between groups. G2 had no significant difference of the perceptions as G1 with p = 0.128. G2 were successfully blinded to placebo US-guided DN.-
dcterms.abstractConclusion-
dcterms.abstractUS-guided DN with exercise therapy may be more effective than traditional DN with exercise therapy or exercise therapy alone in reduce pain of KOA.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationPLoS one, 2022, v. 17, no. 9, e0274990en_US
dcterms.isPartOfPLoS oneen_US
dcterms.issued2022-
dc.identifier.isiWOS:000933365700034-
dc.identifier.scopus2-s2.0-85139278387-
dc.identifier.pmid36178946-
dc.identifier.eissn1932-6203en_US
dc.identifier.artne0274990en_US
dc.description.validate202401 bcvc-
dc.description.oaVersion of Recorden_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextCaritas Institute of Higher Educationen_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryCCen_US
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