- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01291043
Efficacy of Shiatsu in Individuals With Fibromyalgia: a Randomized Clinical Trial
Efficacy of Shiatsu in Pain, Flexibility, Sleep, Anxiety and Quality of Life in Individuals With Fibromyalgia: a Randomized Clinical Trial
Study Overview
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.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Sao Paulo, Brazil, 05403-010
- University of Sao Paulo General Hospital
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
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
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: Control Group
|
|
|
Experimental: Shiatsu Group
|
8-week treatment with two Shiatsu sessions per week (50-minute duration)
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change from baseline in VAS at 8 weeks
Time Frame: baseline and 8 weeks
|
In the VAS the subject marks the intensity of its pain in a 10 centimeter horizontal line
|
baseline and 8 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change from baseline in FIQ at 4 weeks
Time Frame: baseline and 4 weeks
|
The FIQ is composed of ten items, in which higher scores indicate higher impact of fibromyalgia over quality of life
|
baseline and 4 weeks
|
|
Change from baseline in PSQI at 4 weeks
Time Frame: 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.
|
baseline and 4 weeks
|
|
Change from baseline in STAI at 4 weeks
Time Frame: 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.
|
baseline and 4 weeks
|
|
Change from baseline in VSRT at 4 weeks
Time Frame: baseline and 4 weeks
|
The VSRT will be used to assess the flexibility mainly of the hamstring muscles and also of the lower back.
|
baseline and 4 weeks
|
|
Change from baseline in FIQ at 8 weeks
Time Frame: baseline and 8 weeks
|
The FIQ is composed of ten items, in which higher scores indicate higher impact of fibromyalgia over quality of life.
|
baseline and 8 weeks
|
|
Change from baseline in PSQI at 8 weeks
Time Frame: 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.
|
baseline and 8 weeks
|
|
Change from baseline in STAI at 8 weeks
Time Frame: 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.
|
baseline and 8 weeks
|
|
Change from baseline in VSRT at 8 weeks
Time Frame: baseline and 8 weeks
|
The VSRT will be used to assess the flexibility mainly of the hamstring muscles and also of the lower back.
|
baseline and 8 weeks
|
|
Change from baseline in VAS at 4 weeks
Time Frame: Baseline and 4 weeks
|
In the VAS, the subject marks the intensity of its pain in a 10 centimeter horizontal line.
|
Baseline and 4 weeks
|
|
Change from baseline in ABC scale at 4 weeks
Time Frame: 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.
|
baseline and 4 weeks
|
|
Change from baseline in ABC scale at 8 weeks
Time Frame: 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.
|
baseline and 8 weeks
|
|
Change from baseline in PT mean at 4 weeks
Time Frame: baseline and 4 weeks
|
In dolorimetry, the PT of 18 tender points are measured with the dolorimeter.
Then the PT mean will be calculated.
|
baseline and 4 weeks
|
|
Change from baseline in PT mean at 8 weeks
Time Frame: baseline and 8 weeks
|
In dolorimetry, the PT of 18 tender points are measured with the dolorimeter.
Then the PT mean will be calculated.
|
baseline and 8 weeks
|
Collaborators and Investigators
Investigators
- Principal Investigator: Susan LK Yuan, MSc, Faculty of Medicine of the University of São Paulo
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 1297/09
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