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Effects of Whole-Body Vibration Exercise on Serum IGF-1 in Fibromyalgia

I

Institut Nacional d'Educacio Fisica de Catalunya

Status

Completed

Conditions

Fibromyalgia
Hormonal Responses to Exercise in Patients With Fibromyalgia.

Treatments

Device: Placebo Whole-body vibration exercise
Device: Vibratory platform, PowerPlate®, Badhoevendorp, Netherlands

Study type

Interventional

Funder types

Other

Identifiers

NCT00650715
WBVIGF1FM

Details and patient eligibility

About

The purpose of this study was to investigate the acute and chronic effect of whole-body vibration exercise on serum insulin-like growth factor-1 levels in women with fibromyalgia (FM). It was hypothesized that women with FM would exhibit an increase in IGF-1 following both acute and chronic WBV. Twenty-four women with FM were randomized into two groups: Vibration Group (VG) and Control Group (CG). The VG underwent a protocol with WBV exercise twice a week for a total of six weeks, whereas the CG performed the same protocol without vibratory stimulus. Both groups continued with their usual pharmacological treatment. Serum IGF-1 levels were determined using Enzyme-Linked Immunosorbent Assay (ELISA). To test the effect of chronic WBV, serum IGF-1 measurements were taken at baseline and at weeks 1,3, and 6 of intervention. To test the effect of acute WBV, within week 1, serum IGF-1 measurements were taken before and immediately following a session of WBV.

Enrollment

24 patients

Sex

Female

Ages

35 to 69 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients diagnosed of fibromyalgia according to the American College of Rheumatology criteria for at least three years.

Exclusion criteria

  • Orthopedic limitation, or cardiovascular, pulmonary, or metabolic disease that would preclude exercise.
  • Participation in any other study.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

24 participants in 2 patient groups, including a placebo group

VG
Active Comparator group
Description:
Vibration Group (VG) underwent a protocol with whole-body vibration exercise twice a week for a total of six weeks. The group continued with their usual pharmacological treatment.
Treatment:
Device: Vibratory platform, PowerPlate®, Badhoevendorp, Netherlands
CG
Placebo Comparator group
Description:
The Control Group (CG) underwent the same protocol of exercises than VG but without vibratory stimulus. The CG continued with their usual pharmacological treatment.
Treatment:
Device: Placebo Whole-body vibration exercise

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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