Fibromyalgia
Conditions
Interventions
Assessments and reassessments will be carried out at 2 different times, namely: Time 1 (initial or baseline assessment) The experimental group (composed of 45 individuals) and the control group (compo
at the first moment – ??Time 1, the experimental group (composed of 45 individuals) and the control group (composed of 45 individuals) will undergo a standardized musculoskeletal clinical examination.
muscle energy techniques, in which the principle is to place the muscle in the stretched position and asking for an isometric contraction, the isometric contraction of the stretched muscle causes a st
and thrust techniques, in which a manipulation is appli
E02.190.599.280
Sponsors
Escola de Osteopatia de Madrid
Escola de Osteopatia de Madrid
Eligibility
Sex/Gender
Female
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: The inclusion criteria adopted in the study will be: The individuals participating in the study will be (a) women with a medical diagnosis of fibromyalgia or (b) who respond positively to the ACR test, (c) age not less than 18 years and not more than 60 years, (d) with pain for more than 3 months, (e) not pregnant, (f) no history of other concomitant pathologies of rheumatologic origin (rheumatoid arthritis, lupus).
Exclusion criteria
Exclusion criteria: The exclusion criteria are (a) not signing the informed consent form.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is expected to find through pressure algometry an increase in the pressure pain threshold.;It is expected to find through the Pittsburgh Sleep Quality Index (psqi-br) improvement in sleep quality.;.It is expected to find through the SF-36 quality of life questionnaire improvement in quality of life. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary outcomes are not expected. | — |
Countries
Brazil
Contacts
Public ContactDouglas Santos
Outcome results
None listed