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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01912690
Other study ID # TRAINING
Secondary ID
Status Completed
Phase N/A
First received July 29, 2013
Last updated September 20, 2015
Start date July 2013

Study information

Verified date August 2015
Source Hadassah Medical Organization
Contact n/a
Is FDA regulated No
Health authority Israel: Ministry of Health
Study type Interventional

Clinical Trial Summary

The hypothesis of the study is that aerobic conditioning following acute heart attack will improve autonomic function and electrical stability of the heart.


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date
Est. primary completion date January 2015
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- s/p acute myocardial infarction 14-30 days

- ability to perform exercise

Exclusion Criteria:

- unstable angina

- chronic atrial fibrillation

- severely reduced LV function

- NYHA 4

- severe valvular disease

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention


Intervention

Other:
aerobic training

aerobic and strength training


Locations

Country Name City State
Israel Hadassah University Medical Center Jerusalem

Sponsors (1)

Lead Sponsor Collaborator
Hadassah Medical Organization

Country where clinical trial is conducted

Israel, 

Outcome

Type Measure Description Time frame Safety issue
Primary Left ventrcular dyssynchrony Assessed by 2-D strain imaging 3 months No
Secondary Autonomic function Assessed by Holter 3 months No
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