Fybromialgia
Conditions
Interventions
Physical exercise program: Aerobic training with load progression will be developed in a supervised therapist during about 30 minutes each session based on the following protocol: Warm-up phase: The v
Stimulus phase: Pedaled with increased load, in order to maintain Maximum Heart Rate between 75 percent to 80 percent. The volunteers will be encouraged to increase the load if the Maximum Heart Rate
Cooling phase: The volunteers were instructed to perform light and without increasing the load. Stretching of the main muscle groups: biceps, trapezius, latissimus dorsi, pectoral, paraspinal, hamstri
G11.427.590.530.698.277
Sponsors
Universidade Federal de São Paulo - Campus Baixada Santista
Universidade Federal de São Paulo - Campus Baixada Santista
Eligibility
Sex/Gender
Female
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: Volunteers female with aged between 18 and 60 years; with fybromialgia diagnosis according to the fybromialgia diagnostic criteria of the American College of Rheumatology 2016, evaluated by a rheumatologist doctor partner of the project; do not have deficits according to the cut-off score of the Mini Mental State Examination; classified as little active and irregularly active according to the score of the International Physical Activity Questionnaire - short version; interest and availability to participate in the entire experimental protocol
Exclusion criteria
Exclusion criteria: Volunteers with cognitive deficits that prevent the understanding of the assessments and questionnaires involved; who have uncontrolled systemic diseases, such as diabetes mellitus and systemic arterial hypertension; Neurological and musculoskeletal conditions that may directly interfere with assessments, such as paralysis, significant changes in sensitivity, joint diseases at advanced levels (such as arthroplasties or osteoarthritis); Continued use of alcohol or illicit drugs and absolute contraindication for phototherapy such as the presence of neoplasia; volunteers with malnutrition (body mass index less than 18.5) or morbid obesity (body mass index equal to or above 40)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 14% improvement on the Revised Fibromyalgia Impact Questionnaire (FIQR) and 3 point improvement on the Analog Pain Scale. | — |
Secondary
| Measure | Time frame |
|---|---|
| Improvement of 10 points (pain) and 33.3 points (emotional aspect) in the Quality of Life Questionnaire (SF-36), minimum improvement of 0.15 in the fatigue severity scale, minimum improvement of 1.60 seconds in Timed Up-and-Go Test (TTUG) and minimum improvement of 65.20 meters in the 6-minute Walk Test (6MWT) | — |
Countries
Brazil
Contacts
Public ContactAna Balão
Universidade Federal de São Paulo - Campus Baixada Santista
Outcome results
None listed