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Article: Effects of Qigong on late-stage complex regional pain syndrome

TitleEffects of Qigong on late-stage complex regional pain syndrome
Authors
Issue Date1999
PublisherInnoVision Communications. The Journal's web site is located at www.alternative-therapies.com
Citation
Alternative Therapies in Health and Medicine, 1999, v. 5 n. 1, p. 45-54 How to Cite?
AbstractCONTEXT: Despite the growing popularity of qigong in the West, few well-controlled studies using a sham master to assess the clinical efficacy of qigong have been conducted. OBJECTIVE: To study the effect of qigong on treatment-resistant patients with late-stage complex regional pain syndrome type I. DESIGN: Block-random placebo-controlled clinical trial. SETTING: Pain Management Center at New Jersey Medical School. PATIENTS: 26 adult patients (aged 18 to 65 years) with complex regional pain syndrome type I. INTERVENTIONS: The experimental group received qi emission and qigong instruction (including home exercise) by a qigong master. The control group received a similar set of instructions by a sham master. The experimental protocol included 6 forty-minute qigong sessions over 3 weeks, with reevaluation at 6 and 10 weeks. Assessment included comprehensive medical history, physical exam, psychological evaluation, necessary diagnostic testing. Symptom Check List 90, and the Carleton University Responsiveness to Suggestion Scale. MAIN OUTCOME MEASURES: Thermography, swelling, discoloration, muscle wasting, range of motion, pain intensity rating, medication usage, behavior assessment (activity level and domestic disability), frequency of pain awakening, mood assessment, and anxiety assessment. RESULTS: 22 subjects completed the protocol. Among the genuine qigong group, 82% reported less pain by the end of the first training session compared to 45% of control patients. By the last training session, 91% of qigong patients reported analgesia compared to 36% of control patients. Anxiety was reduced in both groups over time, but the reduction was significantly greater in the experimental group than in the control group. CONCLUSIONS: Using a credible placebo to control for nonspecific treatment effects, qigong training was found to result in transient pain reduction and long-term anxiety reduction. The positive findings were not related to preexperimental differences between groups in hypnotizability. Future studies of qigong should control for possible confounding influences and perhaps use clinical disorders more responsive to psychological intervention.
Persistent Identifierhttp://hdl.handle.net/10722/205642
ISSN
2015 Impact Factor: 1.329
2015 SCImago Journal Rankings: 0.497
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorWu, WH-
dc.contributor.authorBandilla, E-
dc.contributor.authorCiccone, DS-
dc.contributor.authorYang, J-
dc.contributor.authorCheng, SCS-
dc.contributor.authorCarner, N-
dc.contributor.authorWu, Y-
dc.contributor.authorShen, R-
dc.date.accessioned2014-09-22T03:07:24Z-
dc.date.available2014-09-22T03:07:24Z-
dc.date.issued1999-
dc.identifier.citationAlternative Therapies in Health and Medicine, 1999, v. 5 n. 1, p. 45-54-
dc.identifier.issn1078-6791-
dc.identifier.urihttp://hdl.handle.net/10722/205642-
dc.description.abstractCONTEXT: Despite the growing popularity of qigong in the West, few well-controlled studies using a sham master to assess the clinical efficacy of qigong have been conducted. OBJECTIVE: To study the effect of qigong on treatment-resistant patients with late-stage complex regional pain syndrome type I. DESIGN: Block-random placebo-controlled clinical trial. SETTING: Pain Management Center at New Jersey Medical School. PATIENTS: 26 adult patients (aged 18 to 65 years) with complex regional pain syndrome type I. INTERVENTIONS: The experimental group received qi emission and qigong instruction (including home exercise) by a qigong master. The control group received a similar set of instructions by a sham master. The experimental protocol included 6 forty-minute qigong sessions over 3 weeks, with reevaluation at 6 and 10 weeks. Assessment included comprehensive medical history, physical exam, psychological evaluation, necessary diagnostic testing. Symptom Check List 90, and the Carleton University Responsiveness to Suggestion Scale. MAIN OUTCOME MEASURES: Thermography, swelling, discoloration, muscle wasting, range of motion, pain intensity rating, medication usage, behavior assessment (activity level and domestic disability), frequency of pain awakening, mood assessment, and anxiety assessment. RESULTS: 22 subjects completed the protocol. Among the genuine qigong group, 82% reported less pain by the end of the first training session compared to 45% of control patients. By the last training session, 91% of qigong patients reported analgesia compared to 36% of control patients. Anxiety was reduced in both groups over time, but the reduction was significantly greater in the experimental group than in the control group. CONCLUSIONS: Using a credible placebo to control for nonspecific treatment effects, qigong training was found to result in transient pain reduction and long-term anxiety reduction. The positive findings were not related to preexperimental differences between groups in hypnotizability. Future studies of qigong should control for possible confounding influences and perhaps use clinical disorders more responsive to psychological intervention.-
dc.languageeng-
dc.publisherInnoVision Communications. The Journal's web site is located at www.alternative-therapies.com-
dc.subject.meshMiddle Aged-
dc.subject.meshReflex Sympathetic Dystrophy - therapy-
dc.subject.meshBreathing Exercises-
dc.subject.meshTreatment Outcome-
dc.subject.meshTime Factors-
dc.titleEffects of Qigong on late-stage complex regional pain syndromeen_US
dc.typeArticleen_US
dc.identifier.emailYang, J: jcsyang@hkucc.hku.hk-
dc.identifier.pmid9893315-
dc.identifier.hkuros44420-
dc.identifier.volume5-
dc.identifier.issue1-
dc.identifier.spage45-
dc.identifier.epage54-
dc.identifier.isiWOS:000077702900020-
dc.publisher.placeUnited States-

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