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High Intensity Interval Training in Acute Pulmonary Embolism

Not Applicable
Conditions
Pulmonary embolism
Acute Pulmonary Embolism.
Registration Number
IRCT20170111031884N2
Lead Sponsor
Vice Chancellor for research,Tehran Heart Center (TUMS)
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
60
Inclusion Criteria

Between 18-70 Years old;
admitted with acute pulmonary embolism confirmed by pulmonary CT angiography
signed informed consent

Exclusion Criteria

History of recurrent pulmonary embolism
Low-risk pulmonary embolism
Unable to participate in an exercise program
Pregnancy
Unable to read and understand the consent form

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Aerobic capacity. Timepoint: before and after 8 weeks. Method of measurement: Bruce modified test.;Right ventricular function. Timepoint: before and after 8 weeks. Method of measurement: Two-dimensional and Doppler echocardiographic.;Pulmonary function. Timepoint: before and after 8 weeks. Method of measurement: Spirometry test.;Quality of life. Timepoint: before and after 8 weeks. Method of measurement: SF36 questionnaire.
Secondary Outcome Measures
NameTimeMethod
Safety. Timepoint: before, during and after intervnetion. Method of measurement: Assessed by recording the number and type of adverse events and any remedial action recorded in the patient’s exercise diary and interventionist records.
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