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Effects of Pain Therapeutic Education and Hydrotherapy on Physical Function, Pain and Sleep of Women With Fibromyalgia

Primary Purpose

Fibromyalgia

Status
Completed
Phase
Not Applicable
Locations
Brazil
Study Type
Interventional
Intervention
Pain Education
Hydrotherapy
Sponsored by
Universidade Federal de Sao Carlos
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Fibromyalgia focused on measuring Hydrotherapy, Pain education

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Clinical and medical Fibromyalgia Diagnosis according to ACR Diagnostic criteria 2010 and 2016;
  • Willing to perform hydrotherapy as treatment.

Exclusion Criteria:

  • Cognitive deficits that prevent volunteers from understanding evaluation and treatment procedures;
  • Uncontrolled systemic illnesses (diabetes, hypertension);
  • Neurological and musculoskeletal conditions that may interfere in the evaluation and treatment procedures (palsies, sensitivity alterations, advanced osteoarthritis);
  • Infecto-contagious illnesses (especially in the urinary tract);
  • Alcohol or drug abuse;
  • Pregnancy.

Sites / Locations

  • Federal University of São Carlos

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Hydrotherapy

Hydrotherapy and Pain Education

Arm Description

Patients allocated to this group will perform 12 weeks of hydrotherapy treatment, with global exercises. Hydrotherapy sessions will last 45 minutes and will be performed twice a week. Exercises will involve aerobic exercises (in the pool) with exercises for upper and lower limbs, and trunk.

Patients allocated to this group will perform 12 weeks of hydrotherapy treatment, with global exercises. Hydrotherapy sessions will last 45 minutes and will be performed twice a week. Exercises will involve aerobic exercises (in the pool) with exercises for upper and lower limbs, and trunk. During the 12 weeks of hydrotherapy treatment, volunteers will also receive 4 sessions of Pain Therapeutic Education, which is also known as Pain Neuroscience Education, which involves patient education on pain neurophysiology, pain chronification and amplification mechanisms, and chronic pain management. These sessions will be performed in specific dates scheduled according to the volunteers' availability, and with intervals that can last from one to two weeks.

Outcomes

Primary Outcome Measures

Changes in Pain throughout time
Visual Analogue Scale (VAS - 100mm) for pain

Secondary Outcome Measures

Changes in number of active myofascial trigger points throughout time
Number of active myofascial trigger points
Changes in depression throughout time
Depression clinical symptoms (measured through Hospital Anxiety and Depression Scale)
Changes in anxiety throughout time
Anxiety clinical symptoms (measured through Hospital Anxiety and Depression Scale)
Changes in Impact of Fibromyalgia in Quality of life throughout time
Quality of life measured through Revised Fibromyalgia Impact Questionnaire
Changes in Quality of life throughout time
Quality of life measured through questionnaire Medical Outcomes Sudy 36-item Short-Form Health Survey (sf-36)
Changes in Sleep throughout time
Sleep quality measured through two questionnaires: Pittsburgh Quality of Sleep Index and Epworth Sleepiness Scale
Changes in Pain neurophysiology learning throughout time
For the Pain Therapeutic Education group, index of Pain Neurophysiology learning with an specific questionnaire
Changes in knowledge of Fibromyalgia throughout time
Fibromyalgia Knowledge will be measured through Fibromyalgia Knowledge Questionnaire
Changes in Appraisal of Self-Care Agency throughout time
Appraissal of Self-Care Agency through The Appraisal of Self-Care Agency Scale - Revised (ASAS-R) scores
Pacient satisfaction with the intervention
Structured questionnaire through which patient will answer about satisfaction with treatment, with a 5-point Likert Scale, with the possible asnswers: "Totally Agree", "Agree", "Neutral", "Disagree" and "Totally Disagree", relative to the following affirmations: 1) I am satisfied with the treatment I received; 2) I believe this treatment was helpful for my condition; 3) I believe my health status has improved after treatment; 4) I will include in my daily life activities things I have learned during my treatment; 5) I will recommend this treatment to someone who has the same health condition as me.
Patient's perception of change
Self-perception of change with the Global Rating of Change Scale; with this scale from -7 to 7, the participant will rate her perception of change after intervention. The negative values will be considered as a worsening in the health status, and the positive values, as a improvement in the health condition of the participant. Zero will be considered as no change in the health status.

Full Information

First Posted
February 20, 2017
Last Updated
November 3, 2020
Sponsor
Universidade Federal de Sao Carlos
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1. Study Identification

Unique Protocol Identification Number
NCT03073642
Brief Title
Effects of Pain Therapeutic Education and Hydrotherapy on Physical Function, Pain and Sleep of Women With Fibromyalgia
Official Title
Effects of Pain Therapeutic Education and Hydrotherapy on Pain, Depression, Anxiety, Quality of Life and Quality of Sleep of Women With Fibromyalgia
Study Type
Interventional

2. Study Status

Record Verification Date
November 2020
Overall Recruitment Status
Completed
Study Start Date
April 1, 2019 (Actual)
Primary Completion Date
October 31, 2020 (Actual)
Study Completion Date
November 3, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Universidade Federal de Sao Carlos

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Fibromyalgia (FM) is a prevalent and disabling disease, that affects mostly women and its main characteristic is chronic pain. Several studies have shown that hydrotherapy is effective in the improvement of symptoms and quality of life of this population; other studies have shown that Pain Therapeutic Education (PTE) is also effective in this sense. PTE is one cheap, easy to apply intervention, with very positive results in chronic pain situations. However, there is a lack of studies that have shown the effects of this intervention on FM. Hence, this study will aim to verify the effectiveness of the hydrotherapy and PTE on women with FM. Sixty women will be randomly allocated in two groups: hydrotherapy and hydrotherapy + PTE. Before treatment start, the investigators will evaluate pain (visual analogue scale, presence of myofascial trigger points and pressure pain threshold over the scalene, upper trapezius, infraspinatus, piriformis, iliopsoas and soleus, bilaterally), quality of life (Fibromyalgia Impact Questionnaire and medical outcomes study 36-item short-form health survey), depression (Beck Depression Inventory), anxiety (Beck Anxiety Inventory) and sleep quality (Pittsburgh Sleep Quality Index and Epworth Sleepiness Scale). Hydrotherapy treatment will last 12 weeks. Women will be evaluated other 3 times: after 6 and 12 weeks (treatment middle and end) and 12 weeks after treatment completion (follow-up). Women in the hydrotherapy group will receive a folder with explanations on FM. Women in the hydrotherapy + PTE will participate of 4 meetings over 12 treatment weeks, in which themes like pain physiology, pain chronification and exacerbation and pain self-management, as well as information on FM will be approached. Statistical analysis will include qualitative and quantitative variable description. Correlation among variables will also be analyzed. Level of significance will be set at 5%.
Detailed Description
The investigators will select at least 80 women with fibromyalgia (FM) for this study, in which pain (through pressure pain threshold and number of active myofascial trigger points), quality of life, FM impact on quality of life and function, depression, anxiety and quality of sleep will be evaluated. After evaluating the volunteer, the participant will be randomly allocated to one of two groups: hydrotherapy treatment (HT), and hydrotherapy treatment together with pain therapeutic education (HT+PTE). All volunteers will perform 12 weeks of hydrotherapy treatment, in which the investigators will perform global exercises for upper and lower limbs and trunk. Volunteers in the HT+PTE group will receive, throughout the 12 weeks of HT, 4 sessions of PTE, in which the investigators will teach pain neurophysiology, pain chronification and pain management. Evaluation sessions will take place before treatment, after 6 and 12 weeks of HT and after 12 weeks of treatment ending. In all evaluations sessions, the investigators will collect data on those aspects previously described.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Fibromyalgia
Keywords
Hydrotherapy, Pain education

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Double blind randomized controlled trial with 1:1 allocation
Masking
Care ProviderInvestigator
Masking Description
Outcomes assessor will not know in which group volunteers are allocated; Care provider will not know outcome measures for any volunteers before study completion.
Allocation
Randomized
Enrollment
90 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Hydrotherapy
Arm Type
Active Comparator
Arm Description
Patients allocated to this group will perform 12 weeks of hydrotherapy treatment, with global exercises. Hydrotherapy sessions will last 45 minutes and will be performed twice a week. Exercises will involve aerobic exercises (in the pool) with exercises for upper and lower limbs, and trunk.
Arm Title
Hydrotherapy and Pain Education
Arm Type
Experimental
Arm Description
Patients allocated to this group will perform 12 weeks of hydrotherapy treatment, with global exercises. Hydrotherapy sessions will last 45 minutes and will be performed twice a week. Exercises will involve aerobic exercises (in the pool) with exercises for upper and lower limbs, and trunk. During the 12 weeks of hydrotherapy treatment, volunteers will also receive 4 sessions of Pain Therapeutic Education, which is also known as Pain Neuroscience Education, which involves patient education on pain neurophysiology, pain chronification and amplification mechanisms, and chronic pain management. These sessions will be performed in specific dates scheduled according to the volunteers' availability, and with intervals that can last from one to two weeks.
Intervention Type
Other
Intervention Name(s)
Pain Education
Other Intervention Name(s)
Pain Neuroscience Education, Pain Therapeutic Education
Intervention Description
Together with hydrotherapy, patients will receive pain therapeutic education
Intervention Type
Other
Intervention Name(s)
Hydrotherapy
Intervention Description
Hydrotherapy sessions, lasting 45 minutes, twice a week for 12 weeks.
Primary Outcome Measure Information:
Title
Changes in Pain throughout time
Description
Visual Analogue Scale (VAS - 100mm) for pain
Time Frame
Before treatment, after 6 and 12 weeks of treatment and after 12 weeks of treatment completion.
Secondary Outcome Measure Information:
Title
Changes in number of active myofascial trigger points throughout time
Description
Number of active myofascial trigger points
Time Frame
Before treatment, after 6 and 12 weeks of treatment and after 12 weeks of treatment completion.
Title
Changes in depression throughout time
Description
Depression clinical symptoms (measured through Hospital Anxiety and Depression Scale)
Time Frame
Before treatment, after 6 and 12 weeks of treatment and after 12 weeks of treatment completion.
Title
Changes in anxiety throughout time
Description
Anxiety clinical symptoms (measured through Hospital Anxiety and Depression Scale)
Time Frame
Before treatment, after 6 and 12 weeks of treatment and after 12 weeks of treatment completion.
Title
Changes in Impact of Fibromyalgia in Quality of life throughout time
Description
Quality of life measured through Revised Fibromyalgia Impact Questionnaire
Time Frame
Before treatment, after 6 and 12 weeks of treatment and after 12 weeks of treatment completion.
Title
Changes in Quality of life throughout time
Description
Quality of life measured through questionnaire Medical Outcomes Sudy 36-item Short-Form Health Survey (sf-36)
Time Frame
Before treatment, after 6 and 12 weeks of treatment and after 12 weeks of treatment completion.
Title
Changes in Sleep throughout time
Description
Sleep quality measured through two questionnaires: Pittsburgh Quality of Sleep Index and Epworth Sleepiness Scale
Time Frame
Before treatment, after 6 and 12 weeks of treatment and after 12 weeks of treatment completion.
Title
Changes in Pain neurophysiology learning throughout time
Description
For the Pain Therapeutic Education group, index of Pain Neurophysiology learning with an specific questionnaire
Time Frame
Before treatment, after 6 and 12 weeks of treatment and after 12 weeks of treatment completion.
Title
Changes in knowledge of Fibromyalgia throughout time
Description
Fibromyalgia Knowledge will be measured through Fibromyalgia Knowledge Questionnaire
Time Frame
Before treatment, after 6 and 12 weeks of treatment and after 12 weeks of treatment completion.
Title
Changes in Appraisal of Self-Care Agency throughout time
Description
Appraissal of Self-Care Agency through The Appraisal of Self-Care Agency Scale - Revised (ASAS-R) scores
Time Frame
Before treatment, after 6 and 12 weeks of treatment and after 12 weeks of treatment completion.
Title
Pacient satisfaction with the intervention
Description
Structured questionnaire through which patient will answer about satisfaction with treatment, with a 5-point Likert Scale, with the possible asnswers: "Totally Agree", "Agree", "Neutral", "Disagree" and "Totally Disagree", relative to the following affirmations: 1) I am satisfied with the treatment I received; 2) I believe this treatment was helpful for my condition; 3) I believe my health status has improved after treatment; 4) I will include in my daily life activities things I have learned during my treatment; 5) I will recommend this treatment to someone who has the same health condition as me.
Time Frame
After 6 and 12 weeks of treatment and after 12 weeks of treatment completion.
Title
Patient's perception of change
Description
Self-perception of change with the Global Rating of Change Scale; with this scale from -7 to 7, the participant will rate her perception of change after intervention. The negative values will be considered as a worsening in the health status, and the positive values, as a improvement in the health condition of the participant. Zero will be considered as no change in the health status.
Time Frame
After 6 and 12 weeks of treatment and after 12 weeks of treatment completion.

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Clinical and medical Fibromyalgia Diagnosis according to ACR Diagnostic criteria 2010 and 2016; Willing to perform hydrotherapy as treatment. Exclusion Criteria: Cognitive deficits that prevent volunteers from understanding evaluation and treatment procedures; Uncontrolled systemic illnesses (diabetes, hypertension); Neurological and musculoskeletal conditions that may interfere in the evaluation and treatment procedures (palsies, sensitivity alterations, advanced osteoarthritis); Infecto-contagious illnesses (especially in the urinary tract); Alcohol or drug abuse; Pregnancy.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mariana A Avila, Ph.D.
Organizational Affiliation
UFSCar
Official's Role
Principal Investigator
Facility Information:
Facility Name
Federal University of São Carlos
City
Sao Carlos
State/Province
SP
ZIP/Postal Code
13565-905
Country
Brazil

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
All results shall be disclosed in a form that no individual volunteers shall be identified.
Citations:
PubMed Identifier
23801009
Citation
Queiroz LP. Worldwide epidemiology of fibromyalgia. Curr Pain Headache Rep. 2013 Aug;17(8):356. doi: 10.1007/s11916-013-0356-5.
Results Reference
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PubMed Identifier
20536907
Citation
Ortega E, Bote ME, Giraldo E, Garcia JJ. Aquatic exercise improves the monocyte pro- and anti-inflammatory cytokine production balance in fibromyalgia patients. Scand J Med Sci Sports. 2012 Feb;22(1):104-12. doi: 10.1111/j.1600-0838.2010.01132.x. Epub 2010 Jun 1.
Results Reference
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Effects of Pain Therapeutic Education and Hydrotherapy on Physical Function, Pain and Sleep of Women With Fibromyalgia

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