Exercise on an exercise bike associated with laser therapy on pain and quality of life in women with fibromyalgia

Not Applicable

Recruiting

• Conditions: Fybromialgia; D012219

• Registration Number: RBR-6gm4ysj
• Lead Sponsor: niversidade Federal de São Paulo - Campus Baixada Santista

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2022-02-25
• Last Update Posted: 29 May 2023
• Study Completion: 2023-11-30

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: Not specified

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

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)

Study & Design

• Study Type: Intervention
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
14% improvement on the Revised Fibromyalgia Impact Questionnaire (FIQR) and 3 point improvement on the Analog Pain Scale.

Secondary Outcome Measures

Name	Time	Method
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)