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Cardiovascular evaluation Exercise in patients with Sjogren's Syndrome

Not Applicable
Conditions
Sjogren's syndrome
M35.0
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
NameTimeMethod
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
NameTimeMethod
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.
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