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Acute Effect of Full-Body Vibration in Women with Fibromyalgia

Acute Effect of Full-Body Vibration Stimulation in Women with Fibromyalgia

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-83kysp
Enrollment
Unknown
Registered
2018-07-25
Start date
2017-04-01
Completion date
Unknown
Last updated
2025-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Fibromyalgia

Interventions

Experimental group: 20 women, aged 35-70 years, with confirmed diagnosis of fibromyalgia, volunteers should be at the site at 7 am and 30 minutes in the morning, fasted for at least 8 hours and should
Device
Other

Sponsors

Universidade Federal dos Vales do Jequitinhonha e Mucuri
Lead Sponsor
Fundação De Amparo a Pesquisa de Minas Gerais
Collaborator

Eligibility

Sex/Gender
Female
Age
35 Years to 70 Years

Inclusion criteria

Inclusion criteria: Women aged 35 to 70 years; with confirmed diagnosis of fibromyalgia between 1 and 3 years; presence of sensitivity in at least 11 of the 18 specific pain points according to the American College of Rheumatology criteria.

Exclusion criteria

Exclusion criteria: Volunteers who present; any concomitant illness that may be exacerbated by physical activity; pregnancy; orthopedic limitations; inflammatory diseases; degenerative diseases; articular; respiratory or cardiovascular diseases; who are being followed up with a psychiatrist; who perform physical activity for the same 2 times a week; (acute hernia, thrombosis, diabetes, epilepsy, metabolic or neuromuscular diseases, orthopedic injuries and prosthetics); use immunosuppressive medication.

Design outcomes

Primary

MeasureTime frame
The VCI is expected to promote changes in redox status that may explain possible mechanisms for understanding the pathophysiology of FM. For determination of redox status parameters, whole blood will be collected aseptically using heparin as anticoagulant. The plasma will be separated by centrifugation and stored at -80øC until the experiments are performed. To evaluate the redox balance, the concentration of thiobarbituric acid (TBARS), total antioxidant capacity (FRAP), antioxidant enzyme superoxide dismutase (SOD) and catalase (CAT) activity of the samples collected before and immediately after the acute training on the platform vibration. ;Determination of the concentration of thiobarbituric acid: reaction of thiobarbituric acid with Malondeiodo, the main product of lipid peroxidation, will be used to determine thiobarbituric acid concentration, according to the method described by Ohkawa et al. (1979).;Determination of FRAP concentration: The total antioxidant capacity assay will be performed according to (BENZIE, et al., 1996). ;Determination of superoxide dismutase activity: The assay to determine SOD activity will be performed according to Srivastava (2007). ;Determination of catalase activity: the assay will be performed according to the method of Nelson and Kiesov (1972).

Secondary

MeasureTime frame
Pain intensity reduction, which will be assessed by applying the visual analogue pain scale (VAS), which varies from 0 to 10 where 0 consists of no pain and 10 the maximum of persistent pain at the moment. ;Perception subjective exertion, through the Borg scale ranging from 6 to 20, where 6 consists effortlessly and 20 the maximum effort that persists at the time, before and immediately after the acute stimulus of whole body vibration in both groups.

Countries

Brazil

Contacts

Public ContactAna Cristina Lacerda

Universidade Federal dos Vales do Jequitinhonha e Mucuri

lacerdaacr@gmail.com+55-038-3532-1200

Outcome results

None listed

Source: REBEC (via WHO ICTRP)