"Cardiac Rehabilitation in Patients With Hypertrophic Cardiomyopathy".
NCT ID: NCT03178357
Last Updated: 2019-03-26
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
NA
60 participants
INTERVENTIONAL
2017-07-10
2020-12-31
Brief Summary
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The main goal of the study will be to evaluate the effectiveness and safety of comprehensive cardiological rehabilitation and telerehabilitation in patients with hypertrophic cardiomyopathy without left ventricular outflow tract obstruction with preserved systolic function. The study is planned to include 30 patients with HCM subjected to physical training and 30 patients with HCM in the control group treated as standard according to current guidelines, not subjected to physical training.
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
OTHER
NONE
Study Groups
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HCM patients with CR
30 HCM patients treated as standard subjected to 4-week hospital cardiac rehabilitation (CR) including psychological care (counseling and / or psychoeducation) and physical training followed by 8 weeks of telerehabilitation in the patient's home (cardiac rehabilitation + standard therapy)
Cardiac rehabilitation + standard therapy
Patients with HCM subjected to cardiological rehabilitation
HCM patients without CR (control group)
30 HCM patients in control group - standard treatment according to current guidelines and outpatient visits with psychological and / or psychoeducational counseling (standard therapy)
Standard therapy
Standard treatment according to current guidelines and outpatient visits with psychological and / or psychoeducational counseling
Interventions
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Cardiac rehabilitation + standard therapy
Patients with HCM subjected to cardiological rehabilitation
Standard therapy
Standard treatment according to current guidelines and outpatient visits with psychological and / or psychoeducational counseling
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
2. Stable general condition (1 month period).
3. NYHA Class II and III.
4. Preserved LV systolic function (LVEF ≥ 50%).
5. Condition after ICD implantation.
6. Written informed consent of the patient to participate in the Program.
7. Completed eighteen years of age.
Exclusion Criteria
2. Uncontrolled hypertension.
3. Advanced atrio-ventricular block.
4. Myocarditis or pericarditis (up to 6 months).
5. Symptomatic aortic stenosis.
6. Acute systemic illness.
7. Intracardiac thrombosis.
8. Significant ischaemia during low intensity exercise test (2 METS, 50W).
9. Uncontrolled diabetes.
10. Pulmonary embolism (up to 6 months).
11. Thrombophlebitis.
12. New episode of AF/Afl.
13. Decrease in systolic blood pressure during exercise.
14. Co-morbidities that limit exercise tolerance and prevent exercise.
18 Years
ALL
No
Sponsors
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National Institute of Cardiology, Warsaw, Poland
OTHER
Responsible Party
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Principal Investigators
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Krzysztof Sadowski
Role: PRINCIPAL_INVESTIGATOR
The Cardinal Stefan Wyszyński Institute of Cardiology
Locations
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The Cardinal Stefan Wyszyński Institute of Cardiology
Warsaw, Masovian Voivodeship, Poland
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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2.1/I/17
Identifier Type: -
Identifier Source: org_study_id
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