Effects of different intensities of Resistance Training, Walking and Stretching in patients with Fibromyalgia Syndrome

Not Applicable

Recruiting

• Conditions: Fibromyalgia; Women; C05.651.324; M01.975

• Registration Number: RBR-74pcmw
• Lead Sponsor: niversidade do Estado de Santa Catarina - UDESC

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2017-09-21
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

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

Inclusion Criteria

Clinical diagnosis of fibromyalgia; Women;
Over 18 years old; Medical certificate for physical exercise

Exclusion Criteria

Present some incapacitating disease for physical exercise.

Study & Design

• Study Type: Intervention
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The primary outcome is pain. The verification of the changes will be carried out each month by the Fibromyalgia Impact Questionnaire and through digital Fischer algometry. At the end of the intervention, a significant reduction of pain is expected.

Secondary Outcome Measures

Name	Time	Method
Quality of life; Depression; Mood States; Anxiety and Sleep Disorders. To obtain the data, the following instruments will be used: Fibromyalgia impact questionnaire - quality of life - Beck Depression Inventory, Brunel mood states, Beck Anxiety Inventory and Pittsburgh Sleep Quality Index. Evaluations will be held each month. A significant reduction of these variables is expected at the end of the intervention.