Efficacy of Shiatsu in Individuals With Fibromyalgia: a Randomized Clinical Trial
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| First Received Date ICMJE | January 27, 2011 | ||||||||
| Last Updated Date | November 14, 2012 | ||||||||
| Start Date ICMJE | July 2010 | ||||||||
| Primary Completion Date | November 2011 (final data collection date for primary outcome measure) | ||||||||
| Current Primary Outcome Measures ICMJE |
Change from baseline in VAS at 8 weeks [ Time Frame: baseline and 8 weeks ] [ Designated as safety issue: No ] In the VAS the subject marks the intensity of its pain in a 10 centimeter horizontal line |
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| Original Primary Outcome Measures ICMJE |
Change from baseline in pain at 8 weeks [ Time Frame: baseline and 8 weeks ] [ Designated as safety issue: No ] Pain will be evaluated by the following instruments: visual analogue scale, in which the subject marks the intensity of its pain in a 10 cm horizontal line; pain map, in which the subject marks its painful areas; and dolorimetry, in which the pain thresholds of 18 tender points are measured with the dolorimeter. |
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| Change History | Complete list of historical versions of study NCT01291043 on ClinicalTrials.gov Archive Site | ||||||||
| Current Secondary Outcome Measures ICMJE |
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| Original Secondary Outcome Measures ICMJE |
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| Current Other Outcome Measures ICMJE | Not Provided | ||||||||
| Original Other Outcome Measures ICMJE | Not Provided | ||||||||
| Descriptive Information | |||||||||
| Brief Title ICMJE | Efficacy of Shiatsu in Individuals With Fibromyalgia: a Randomized Clinical Trial | ||||||||
| Official Title ICMJE | Efficacy of Shiatsu in Pain, Flexibility, Sleep, Anxiety and Quality of Life in Individuals With Fibromyalgia: a Randomized Clinical Trial | ||||||||
| Brief Summary | Fibromyalgia is a syndrome characterized by chronic and generalized musculoskeletal pain and tenderness in tender points. Its etiology and physiopathology are not well known; therefore its treatment is not satisfactory. Having this in view, a search for alternative and complementary medicine has been going on. This kind of practice is under pressure to present evidences of efficacy. A randomized clinical trial will be carried out with the aim of verifying the efficacy of a massage technique called Shiatsu in the improvement of pain, flexibility, quality of sleep, anxiety and quality of life of individuals with fibromyalgia. A sample of 34 subjects will be divided in Shiatsu Group and Control Group. All subjects will be evaluated in the beginning, in the middle and at the end of the treatment. Pain will be evaluated by the following instruments: visual analogue scale (VAS) and dolorimetry. The V-sit and reach test (VSRT) will be used to assess the flexibility of the hamstring muscles and lower back. The sleep will be evaluated with the Pittsburgh Sleep Quality Index (PSQI). The State-Trait Anxiety Inventory (STAI) will be used to evaluate anxiety. The evaluation of quality of life will be made with two instruments: fibromyalgia impact questionnaire (FIQ) and Activities-specific Balance Confidence (ABC) scale. In each treatment session, the subjects will be globally evaluated in the 14 main meridians and their respective points by touch, identifying points of excessive energy and their severity. The Control Group will wait for treatment and remain only with conventional pharmacological treatment, while the Shiatsu Group will receive a treatment with Shiatsu during eight weeks. The results will be expressed in mean and standard deviation. The normality of the data will be verified by the Shapiro-Wilk test. In the intragroup analysis, the T-test for the parametric data and the Wilcoxon test for the nonparametric data. In the comparison between groups, the analysis of variance (ANOVA) test will be used. The level of significance adopted will be α < 0.05. |
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| Detailed Description | In the VAS, the subject marks the intensity of its pain in a 10 centimeter horizontal line. In dolorimetry, the pain thresholds (PT) of 18 tender points are measured with the dolorimeter. The VSRT assesses the flexibility mainly of the hamstring muscles and also of the lower back. The PSQI is constituted of 19 questions. Scores of five or more indicate bad sleep quality and sleep disturbances. The STAI is composed of two scales of items with semantic content which expresses the absence or presence of anxiety. Higher scores obtained in each scale indicate higher levels of anxiety. The FIQ is composed of ten items. Higher scores indicate higher impact of fibromyalgia over quality of life The ABC scale was translated and adapted for this study and consists of a 17-item scale in which the level of confidence in balance is indicated in the execution of diverse activities. |
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| Study Type ICMJE | Interventional | ||||||||
| Study Phase | Not Provided | ||||||||
| Study Design ICMJE | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Treatment |
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| Condition ICMJE | Fibromyalgia | ||||||||
| Intervention ICMJE | Other: Shiatsu
8-week treatment with two Shiatsu sessions per week (50-minute duration)
Other Name: Acupressure |
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| Study Arm (s) |
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| Publications * | Not Provided | ||||||||
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* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline. |
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| Recruitment Information | |||||||||
| Recruitment Status ICMJE | Completed | ||||||||
| Enrollment ICMJE | 34 | ||||||||
| Completion Date | November 2011 | ||||||||
| Primary Completion Date | November 2011 (final data collection date for primary outcome measure) | ||||||||
| Eligibility Criteria ICMJE | Inclusion Criteria:
Exclusion Criteria:
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| Gender | Both | ||||||||
| Ages | 30 Years to 60 Years | ||||||||
| Accepts Healthy Volunteers | No | ||||||||
| Contacts ICMJE | Contact information is only displayed when the study is recruiting subjects | ||||||||
| Location Countries ICMJE | Brazil | ||||||||
| Administrative Information | |||||||||
| NCT Number ICMJE | NCT01291043 | ||||||||
| Other Study ID Numbers ICMJE | 1297/09 | ||||||||
| Has Data Monitoring Committee | No | ||||||||
| Responsible Party | Susan Yuan, University of Sao Paulo General Hospital | ||||||||
| Study Sponsor ICMJE | University of Sao Paulo General Hospital | ||||||||
| Collaborators ICMJE | Not Provided | ||||||||
| Investigators ICMJE |
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| Information Provided By | University of Sao Paulo General Hospital | ||||||||
| Verification Date | November 2012 | ||||||||
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ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP |
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