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Deep Heat Application in Women with Fibromyalgia

Not Applicable
Conditions
Fibromyalgia
C23.888.592.612
Registration Number
RBR-9szgmpp
Lead Sponsor
Instituto de Neurologia, Neurocirurgia e Comportamento
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot yet recruiting
Sex
Female
Target Recruitment
Not specified
Inclusion Criteria

Women; over 18 years of age; with fibromyalgia; one year of diagnosis; accepted to participate in the intervention

Exclusion Criteria

Women with metallic implants at the application site; with sensitivity alterations at the application site; with silicone prostheses; with a cardiac pacemaker; with neoplasms; with acute inflammatory processes; who are pregnant; with ischemic tissues; with tuberculous lesions; who have had recent deep vein thrombosis; with hemorrhagic conditions or the likelihood of this occurring; with heart disease; with decompensated blood pressure; who have attendance lower than 75% at the appointments/treatment.

Study & Design

Study Type
Intervention
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To investigate whether radiofrequency can modify the pain symptomatology of fibromyalgia as well as to evaluate its impact or not.
Secondary Outcome Measures
NameTimeMethod
To correlate whether the use of radiofrequency in fibromyalgia can change the quality of life index for fibromyalgia.<br>;To determine whether the use of radiofrequency decreases the incidence of pain crises in fibromyalgia. ;To measure the degree of pain intensity before, during and after treatment with radiofrequency. ;To correlate chronic pain with sleep disturbances.
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