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Heart Rate Variability in Fibromyalgia - Effects of Strengthening Exercises

Primary Purpose

Fibromyalgia

Status
Completed
Phase
Phase 4
Locations
Brazil
Study Type
Interventional
Intervention
strengthening exercise
flexibility exercise
Sponsored by
Federal University of Espirito Santo
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Fibromyalgia focused on measuring autonomic nervous system, fibromyalgia, autonomic dysfunction, strengthening, flexibility, exercise, heart rate variability

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Classification criteria for Fibromyalgia (ACR 1990)
  • Sedentary subjects (without regular physical activity in the last 3 months)
  • Women between 18 to 65 years old

Exclusion Criteria:

  • Cardiovascular and/or respiratory diseases that might limit physical activity (COPD, Pulmonary Fibrosis, asthma moderate to severe, respiratory insufficiency);
  • Organ dysfunction (renal, hepatic, coronary, pulmonary insufficiency);
  • Arterial hypertension and diabetes mellitus;
  • Uncontrolled thyroid disease;
  • Autoimmune rheumatic diseases and/or non-autoimmune with symptoms that might limit the movement or physical effort;
  • The use of beta blockers, calcium channel blockers and any other anti-hypertensive, anticonvulsants; non tricycles antidepressants; opioid analgesic including tramadol.
  • cyclobenzaprine >10 mg/day, and amtriptyline > 25 mg/day;
  • Performing or have performed exercise within the last 3 months;
  • Inability to understand the questionnaires;
  • Positive treadmill test for myocardial ischemia;
  • Receipt of the social security benefits.

Sites / Locations

  • Valéria Valim

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

strengthening exercise

Flexibility exercise

Arm Description

The experimental group (STRE) will receive strengthening training in "Station for lifting weight exercises" (Flex Mega 8, Flex Fitness Equipment Brand) using the recommendations of the American College of Sports Medicine (ACMS, 2010), twice a week, during 45 minutes for 16 weeks.

The control group (FLEX) will receive stretching and flexibility exercise training according to the protocol of prescription and previously tested and described in appendix F (Valim et al., 2003), twice a week, during 45 minutes for 16 weeks.

Outcomes

Primary Outcome Measures

pain
Visual analogic scale

Secondary Outcome Measures

Fibromyalgia Impact Questionnaire
Symptoms
Short Form Health Survey
State-Trait Anxiety Inventory (IDATE)
Mood evaluation
BECK Depression Inventory
Mood evaluation
Treadmill test
cardiorespiratory fitness cardiovascular risk
Sit and Reach Test
flexibility
dynamometry
global strength
Maximal repetition test
muscle strength
autonomic modulation
Ratio low frequecy to high frequency in the Heart rate variability

Full Information

First Posted
November 26, 2013
Last Updated
December 6, 2013
Sponsor
Federal University of Espirito Santo
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1. Study Identification

Unique Protocol Identification Number
NCT02004405
Brief Title
Heart Rate Variability in Fibromyalgia - Effects of Strengthening Exercises
Official Title
The Study of Heart Rate Variability in Patients With Fibromyalgia - Effects of Strengthening Exercises
Study Type
Interventional

2. Study Status

Record Verification Date
December 2013
Overall Recruitment Status
Completed
Study Start Date
July 2010 (undefined)
Primary Completion Date
September 2012 (Actual)
Study Completion Date
September 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Federal University of Espirito Santo

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Abstract Objective: Autonomic dysfunction is an important mechanism that could explain many symptoms observed in fibromyalgia (FM). Exercise is an effective treatment, with benefits potentially mediated through changes in autonomic modulation. Strengthening is one of the less studied exercises in FM, and the acute and chronic effects of strengthening on the autonomic system remain unknown. The objective of this study is to assess the effects of strengthening exercises (STRE) on autonomic modulation, pain perception and the quality of life (QOL) of FM patients. Methods: Sedentary women with FM (ACR 1990) will be randomly selected to STRE or flexibility (FLEX) exercises in a blind controlled trial. The intensity of STRE will be set at 45% of the estimated load of 1 Repetition Maximum (RM) in 12 different exercises. The primary outcomes will be pain measured using the Visual Analog Scale (VAS) and the Heart Rate Variability (HRV) analysis. Other outcomes will be assess: fitness measured by treadmill test, the sit and reach test (Wells and Dillon's Bench), handgrip dynamometry; and quality of life by the Fibromyalgia Impact Questionnaire (FIQ), the Beck and Idate Trait-State Inventory (IDATE), a short-form health survey (SF-36). Statistical analyses and ethical procedures: The visual analog scale (VAS) for pain will be the primary measure used to determine sample size. Statistical significance will be set at 5% and power of 80%. These led to at least 58 participants to be randomized. The main hypothesis is that strengthening exercise is a better treatment than flexibility exercise to improve pain, HRV and quality of life. In all measures tested we will consider the null hypothesis (H0) as being the point of equality between groups tested and H1 the point of difference. Bilateral tests were carried out adopting a 5% level of significance. The normality of the results will be tested using the Shapiro-Wilk test. Student's "t"-test for paired samples will be used to perform intra-group comparisons at different times, when the data were normally distributed, and the nonparametric equivalent of Student's t-test (Wilcoxon test) will be used when the data show an asymmetrical distribution. To compare the data between the STRE and FLEX groups, ANOVA for repeated measures will be used, followed by post-hoc Bonferroni's test.
Detailed Description
STUDY PROTOCOL: The experimental group (STRE) will receive strengthening training in "Station for lifting weight exercises" (Flex Mega 8, Flex Fitness Equipment Brand) using the recommendations of the American College of Sports Medicine (ACMS, 2010), twice a week, during 45 minutes for 16 weeks. The control group (FLEX) will receive stretching and flexibility exercise training according to the protocol of prescription and previously tested and described in appendix F (Valim et al., 2003), twice a week, during 45 minutes for 16 weeks. The minimum number of patients per group will be 30. The randomization will be by arriving order of the patients at the Clinic, having 2 groups with a distribution at random one by one. There will be an examiner for the selection and unblinded randomization and another for the application of tools that will be blind. Patients will undergo clinical and cardiological evaluation with an exercise stress test (Ergometric test) request in all of them according to ACMS as one more method of evaluation for inclusion and exclusion. The evaluation will be performed by a blind examiner, an expert physiotherapist in rheumatology and trained for the application of the tools at the beginning, after 30, 60, 90, 120 days from the treatment onset. The measure for prescription and muscle strength gain will be by the method of maximal repetitions (Lindh et al., 1994; Tritschler, 2003; Brosseau et al., 2008; ACSM, 2010). The evaluations will take place at the beginning, 30, 60, 90, 120 days (final evaluation). Evaluations will be performed by the same blind examiner for the examined group. The training team will be formed by a physiotherapist, physical educator, and experienced doctors at strengthening training and flexibility and stretching exercises and they must follow the following protocol. PROTOCOL OF EXERCISES The strength training will be performed according to American College of Sports Medicine (ACSM) and will have a mild to moderate intensity representing 45% of the estimated 1RM obtained from the maximal repetition method. Eight major muscle groups will be trained (quadriceps femoris, hamstrings, biceps brachii, triceps brachii, pectoral, calf, deltoid, and latissimus dorsi) in 12 different exercises, with 3 sets of 12 repetitions (leg Press, leg extension, hip flexion, pectoral fly, triceps extension, shoulder flexion, leg curl, calf, pulldown, shoulder abduction, biceps flexion and shoulder extension). Theses 12 different exercises will be distributed in a composed circuit system of 2 sets of exercises: Set A ((leg Press, leg extension, hip flexion, pectoral fly, triceps extension, shoulder flexion) and set B (leg curl, calf, pulldown, shoulder abduction, biceps flexion and shoulder extension). Each set will be applied once a week alternatively. The exercises will be performed twice a week during 16 weeks. During the training process a load increase will be performed in order to seek progressive muscle strengthening improvement in a controlled way and according to patients' clinical evolution. Blood pressure and heart rate will be monitored as well. Strength and strengthening training will be performed at the Evaluation, Physical Conditioning and Rehabilitation Laboratory (LACORE) at the University Hospital in in Federal University of Espirito Santo. We have chosen the frequency of twice a week because it is a frequency (for this kind of study) validated in the literature (Figueroa et al., 2008, Kingsley et al., 2009; 2010).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Fibromyalgia
Keywords
autonomic nervous system, fibromyalgia, autonomic dysfunction, strengthening, flexibility, exercise, heart rate variability

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
66 (Actual)

8. Arms, Groups, and Interventions

Arm Title
strengthening exercise
Arm Type
Experimental
Arm Description
The experimental group (STRE) will receive strengthening training in "Station for lifting weight exercises" (Flex Mega 8, Flex Fitness Equipment Brand) using the recommendations of the American College of Sports Medicine (ACMS, 2010), twice a week, during 45 minutes for 16 weeks.
Arm Title
Flexibility exercise
Arm Type
Active Comparator
Arm Description
The control group (FLEX) will receive stretching and flexibility exercise training according to the protocol of prescription and previously tested and described in appendix F (Valim et al., 2003), twice a week, during 45 minutes for 16 weeks.
Intervention Type
Other
Intervention Name(s)
strengthening exercise
Intervention Description
The experimental group (STRE) will receive strengthening training in "Station for lifting weight exercises" (Flex Mega 8, Flex Fitness Equipment Brand) using the recommendations of the American College of Sports Medicine (ACMS, 2010), twice a week, during 45 minutes for 16 weeks.
Intervention Type
Other
Intervention Name(s)
flexibility exercise
Intervention Description
The control group (FLEX) will receive stretching and flexibility exercise training according to the protocol of prescription and previously tested and described in appendix F (Valim et al., 2003), twice a week, during 45 minutes for 16 weeks.
Primary Outcome Measure Information:
Title
pain
Description
Visual analogic scale
Time Frame
4 weeks
Secondary Outcome Measure Information:
Title
Fibromyalgia Impact Questionnaire
Description
Symptoms
Time Frame
Initial, 8 weeks, 16 weeks
Title
Short Form Health Survey
Time Frame
Initial, 8 weeks, 16 weeks
Title
State-Trait Anxiety Inventory (IDATE)
Description
Mood evaluation
Time Frame
initial, 8 weeks, 16 weeks
Title
BECK Depression Inventory
Description
Mood evaluation
Time Frame
Initial, 8 weeks, 16 weeks
Title
Treadmill test
Description
cardiorespiratory fitness cardiovascular risk
Time Frame
initial and 16 weeks
Title
Sit and Reach Test
Description
flexibility
Time Frame
4 weeks
Title
dynamometry
Description
global strength
Time Frame
4 weeks
Title
Maximal repetition test
Description
muscle strength
Time Frame
4 weeks
Title
autonomic modulation
Description
Ratio low frequecy to high frequency in the Heart rate variability
Time Frame
4 weeks

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Classification criteria for Fibromyalgia (ACR 1990) Sedentary subjects (without regular physical activity in the last 3 months) Women between 18 to 65 years old Exclusion Criteria: Cardiovascular and/or respiratory diseases that might limit physical activity (COPD, Pulmonary Fibrosis, asthma moderate to severe, respiratory insufficiency); Organ dysfunction (renal, hepatic, coronary, pulmonary insufficiency); Arterial hypertension and diabetes mellitus; Uncontrolled thyroid disease; Autoimmune rheumatic diseases and/or non-autoimmune with symptoms that might limit the movement or physical effort; The use of beta blockers, calcium channel blockers and any other anti-hypertensive, anticonvulsants; non tricycles antidepressants; opioid analgesic including tramadol. cyclobenzaprine >10 mg/day, and amtriptyline > 25 mg/day; Performing or have performed exercise within the last 3 months; Inability to understand the questionnaires; Positive treadmill test for myocardial ischemia; Receipt of the social security benefits.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Maria Bernadete RO Gavi, Master
Organizational Affiliation
Federal University of Espírito Santo
Official's Role
Principal Investigator
Facility Information:
Facility Name
Valéria Valim
City
Vitória
State/Province
Espírito Santo
ZIP/Postal Code
29055020
Country
Brazil

12. IPD Sharing Statement

Citations:
PubMed Identifier
24651512
Citation
Gavi MB, Vassalo DV, Amaral FT, Macedo DC, Gava PL, Dantas EM, Valim V. Strengthening exercises improve symptoms and quality of life but do not change autonomic modulation in fibromyalgia: a randomized clinical trial. PLoS One. 2014 Mar 20;9(3):e90767. doi: 10.1371/journal.pone.0090767. eCollection 2014.
Results Reference
derived

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Heart Rate Variability in Fibromyalgia - Effects of Strengthening Exercises

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