Comparative effectiveness of Chuna manual therapy versus conventional usual care for non-acute low back pain: a pilot randomized controlled trial
Autor: | Koh-Woon Kim, Jae-Heung Cho, Kyeong-Tae Lim, Jae-Young Jung, Min ho Lee A, Me-riong Kim, In-Hyuk Ha, Byung-Cheul Shin, Eui-Hyoung Hwang, Nam-Kwen Kim, Junhwan Lee, Kibong Nam |
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Rok vydání: | 2019 |
Předmět: |
Adult
Male congenital hereditary and neonatal diseases and abnormalities medicine.medical_specialty Medicine (miscellaneous) Pilot Projects law.invention 03 medical and health sciences 0302 clinical medicine Lumbar Randomized controlled trial law medicine Humans Low back pain Pharmacology (medical) Generalizability theory 030212 general & internal medicine Range of Motion Articular Comparative effectiveness research Pilot study lcsh:R5-920 business.industry Research Middle Aged Musculoskeletal Manipulations nervous system diseases Oswestry Disability Index Clinical research Chuna manual therapy Physical therapy Female medicine.symptom Manual therapy lcsh:Medicine (General) business Range of motion 030217 neurology & neurosurgery |
Zdroj: | Trials, Vol 20, Iss 1, Pp 1-8 (2019) Trials |
ISSN: | 1745-6215 |
DOI: | 10.1186/s13063-019-3302-y |
Popis: | Background Low back pain (LBP) is common, with a lifetime prevalence of 80%, and as such it places substantial social and economic burden on individuals and society. Chuna manual therapy (CMT) combines aspects of physiology, biodynamics of spine and joint motion, and basic theory of movement dynamics. This study aimed to test the comparative effectiveness and safety of CMT for non-acute LBP. Methods A three-arm, multicenter, pragmatic, randomized controlled pilot trial was conducted from 28 March 2016 to 19 September 2016, at four medical institutions. A total of 60 patients were randomly allocated to the CMT group (n = 20), usual care (UC) group (n = 20), or combined treatment (CMT + UC) group (n = 20), and received the relevant treatments for 6 weeks. The primary outcome was a numeric rating scale (NRS) representation of LBP intensity, while secondary outcomes included NRS of leg pain, Oswestry disability index (ODI), Patient Global Impression of Change (PGIC), the EuroQol-5 dimensions (EQ-5D), lumbar range of motion, and safety. Results A total of 60 patients were included in the intention-to-treat analysis and 55 patients (CMT, 18; UC, 18; CMT + UC, 19) were included in the per-protocol analysis (drop-out rate 5.3%). Over the treatment period there were significant differences in the NRS score for LBP (CMT mean − 3.28 (95% CI − 4.08, − 2.47); UC − 1.95 (− 2.82, − 1.08); CMT + UC − 1.75 (− 2.70, − 0.80), P |
Databáze: | OpenAIRE |
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