Cardiovascular evaluation Exercise in patients with Sjogren's Syndrome
Not Applicable
- Conditions
- Sjogren's syndromeM35.0
- Registration Number
- RBR-3v3zmd
- Lead Sponsor
- niversidade Federal de São Paulo
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruitment completed
- Sex
- Female
- Target Recruitment
- Not specified
Inclusion Criteria
Women with diagnosis of primary Sjogren's syndrome confirmed by the revised Classification Criteria of 2002; age between 18 and 90 years; understanding and signing of the free and informed consent term.
Exclusion Criteria
Diagnosis of heart, lung, endocrine, or any other disease that impedes the practice of exercise;
Inflammatory joint activity that impedes the practice of exercise; Regular exercise for more than 4 weeks in the last 6 months.
Study & Design
- Study Type
- Intervention
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 15% improvement in maximum oxygen consumption (VO2max) measured by ergospirometry in relation to baseline, performed at the beginning of the study and up to 72 hours after the last training.
- Secondary Outcome Measures
Name Time Method Improvement of respiratory threshold and maximal heart rate as measured by ergospirometry; improvement of ejection fraction and left ventricular systolic and diastolic functions, measured by echocardiography; improvement of glycemic and lipemic profiles; improvement in the quality of life measured by the SF 36 questionnaire; maintenance of the disease activity index measured by the ESSDAI questionnaire. All measurements were taken up to 72 hours after the last training.