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Efficacy of Shiatsu in Individuals With Fibromyalgia: a Randomized Clinical Trial

Primary Purpose

Fibromyalgia

Status
Completed
Phase
Not Applicable
Locations
Brazil
Study Type
Interventional
Intervention
Shiatsu
Sponsored by
University of Sao Paulo General Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Fibromyalgia focused on measuring Shiatsu, Fibromyalgia, Pain, Quality of sleep, Balance, Quality of life

Eligibility Criteria

30 Years - 60 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • diagnoses of fibromyalgia

Exclusion Criteria:

  • 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

Sites / Locations

  • University of Sao Paulo General Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Shiatsu Group

Control Group

Arm Description

Outcomes

Primary Outcome Measures

Change from baseline in VAS at 8 weeks
In the VAS the subject marks the intensity of its pain in a 10 centimeter horizontal line

Secondary Outcome Measures

Change from baseline in FIQ at 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
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
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
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
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
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
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
The VSRT will be used to assess the flexibility mainly of the hamstring muscles and also of the lower back.
Change from baseline in VAS at 4 weeks
In the VAS, the subject marks the intensity of its pain in a 10 centimeter horizontal line.
Change from baseline in ABC scale at 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
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
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
In dolorimetry, the PT of 18 tender points are measured with the dolorimeter. Then the PT mean will be calculated.

Full Information

First Posted
January 27, 2011
Last Updated
November 14, 2012
Sponsor
University of Sao Paulo General Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT01291043
Brief Title
Efficacy of Shiatsu in Individuals With Fibromyalgia: a Randomized Clinical Trial
Official Title
Efficacy of Shiatsu in Pain, Flexibility, Sleep, Anxiety and Quality of Life in Individuals With Fibromyalgia: a Randomized Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
November 2012
Overall Recruitment Status
Completed
Study Start Date
July 2010 (undefined)
Primary Completion Date
November 2011 (Actual)
Study Completion Date
November 2011 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Sao Paulo General Hospital

4. Oversight

Data Monitoring Committee
No

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Fibromyalgia
Keywords
Shiatsu, Fibromyalgia, Pain, Quality of sleep, Balance, Quality of life

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
34 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Shiatsu Group
Arm Type
Experimental
Arm Title
Control Group
Arm Type
No Intervention
Intervention Type
Other
Intervention Name(s)
Shiatsu
Other Intervention Name(s)
Acupressure
Intervention Description
8-week treatment with two Shiatsu sessions per week (50-minute duration)
Primary Outcome Measure Information:
Title
Change from baseline in VAS at 8 weeks
Description
In the VAS the subject marks the intensity of its pain in a 10 centimeter horizontal line
Time Frame
baseline and 8 weeks
Secondary Outcome Measure Information:
Title
Change from baseline in FIQ at 4 weeks
Description
The FIQ is composed of ten items, in which higher scores indicate higher impact of fibromyalgia over quality of life
Time Frame
baseline and 4 weeks
Title
Change from baseline in PSQI at 4 weeks
Description
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.
Time Frame
baseline and 4 weeks
Title
Change from baseline in STAI at 4 weeks
Description
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.
Time Frame
baseline and 4 weeks
Title
Change from baseline in VSRT at 4 weeks
Description
The VSRT will be used to assess the flexibility mainly of the hamstring muscles and also of the lower back.
Time Frame
baseline and 4 weeks
Title
Change from baseline in FIQ at 8 weeks
Description
The FIQ is composed of ten items, in which higher scores indicate higher impact of fibromyalgia over quality of life.
Time Frame
baseline and 8 weeks
Title
Change from baseline in PSQI at 8 weeks
Description
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.
Time Frame
baseline and 8 weeks
Title
Change from baseline in STAI at 8 weeks
Description
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.
Time Frame
baseline and 8 weeks
Title
Change from baseline in VSRT at 8 weeks
Description
The VSRT will be used to assess the flexibility mainly of the hamstring muscles and also of the lower back.
Time Frame
baseline and 8 weeks
Title
Change from baseline in VAS at 4 weeks
Description
In the VAS, the subject marks the intensity of its pain in a 10 centimeter horizontal line.
Time Frame
Baseline and 4 weeks
Title
Change from baseline in ABC scale at 4 weeks
Description
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.
Time Frame
baseline and 4 weeks
Title
Change from baseline in ABC scale at 8 weeks
Description
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.
Time Frame
baseline and 8 weeks
Title
Change from baseline in PT mean at 4 weeks
Description
In dolorimetry, the PT of 18 tender points are measured with the dolorimeter. Then the PT mean will be calculated.
Time Frame
baseline and 4 weeks
Title
Change from baseline in PT mean at 8 weeks
Description
In dolorimetry, the PT of 18 tender points are measured with the dolorimeter. Then the PT mean will be calculated.
Time Frame
baseline and 8 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
30 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: diagnoses of fibromyalgia Exclusion Criteria: 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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Susan LK Yuan, MSc
Organizational Affiliation
Faculty of Medicine of the University of Sao Paulo
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Amelia P Marques, PhD
Organizational Affiliation
Faculty of Medicine of the University of Sao Paulo
Official's Role
Study Director
Facility Information:
Facility Name
University of Sao Paulo General Hospital
City
Sao Paulo
ZIP/Postal Code
05403-010
Country
Brazil

12. IPD Sharing Statement

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Efficacy of Shiatsu in Individuals With Fibromyalgia: a Randomized Clinical Trial

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