Efficacy of Shiatsu in Individuals With Fibromyalgia: a Randomized Clinical Trial
- Conditions
- Fibromyalgia
- Interventions
- Other: Shiatsu
- Registration Number
- NCT01291043
- Lead Sponsor
- University of Sao Paulo General Hospital
- 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.
- 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.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 34
- diagnoses of fibromyalgia
- diagnoses of diseases that cause chronic pain
- skin lesions and infection
- pregnancy
- two consecutive absences in treatment sessions
- use of psychotherapy, physiotherapy or complementary therapies in the last 6 months
- regular supervised physical activity
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Shiatsu Group Shiatsu -
- Primary Outcome Measures
Name Time Method Change from baseline in VAS at 8 weeks baseline and 8 weeks In the VAS the subject marks the intensity of its pain in a 10 centimeter horizontal line
- Secondary Outcome Measures
Name Time Method Change from baseline in VAS at 4 weeks Baseline and 4 weeks In the VAS, the subject marks the intensity of its pain in a 10 centimeter horizontal line.
Change from baseline in FIQ at 4 weeks baseline and 4 weeks The FIQ is composed of ten items, in which higher scores indicate higher impact of fibromyalgia over quality of life
Change from baseline in PSQI at 4 weeks baseline and 4 weeks The sleep will be evaluated with the PSQI, which is constituted of 19 questions. Scores of five or more indicate bad sleep quality and sleep disturbances.
Change from baseline in STAI at 4 weeks baseline and 4 weeks The STAI will be used to evaluate anxiety. It is composed of two scales of items with semantic content which expresses the absence or presence of anxiety. Higher scores indicate higher levels of anxiety.
Change from baseline in VSRT at 4 weeks baseline and 4 weeks The VSRT will be used to assess the flexibility mainly of the hamstring muscles and also of the lower back.
Change from baseline in FIQ at 8 weeks baseline and 8 weeks The FIQ is composed of ten items, in which higher scores indicate higher impact of fibromyalgia over quality of life.
Change from baseline in PSQI at 8 weeks baseline and 8 weeks The sleep will be evaluated with the PSQI, which is constituted of 19 questions. Scores of five or more indicate bad sleep quality and sleep disturbances.
Change from baseline in STAI at 8 weeks baseline and 8 weeks The STAI will be used to evaluate anxiety. It is composed of two scales of items with semantic content which expresses the absence or presence of anxiety. Higher scores indicate higher levels of anxiety.
Change from baseline in VSRT at 8 weeks baseline and 8 weeks The VSRT will be used to assess the flexibility mainly of the hamstring muscles and also of the lower back.
Change from baseline in ABC scale at 4 weeks baseline and 4 weeks 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.
Change from baseline in ABC scale at 8 weeks baseline and 8 weeks 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.
Change from baseline in PT mean at 4 weeks baseline and 4 weeks In dolorimetry, the PT of 18 tender points are measured with the dolorimeter. Then the PT mean will be calculated.
Change from baseline in PT mean at 8 weeks baseline and 8 weeks In dolorimetry, the PT of 18 tender points are measured with the dolorimeter. Then the PT mean will be calculated.
Trial Locations
- Locations (1)
University of Sao Paulo General Hospital
🇧🇷Sao Paulo, Brazil