Aerobic Exercise Training & the Autonomic System In Patients After Myocardial Infarction or Stroke
Recruitment status was Not yet recruiting
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Purpose
The purpose of this study is to examine the effect of Aerobic Physical Activity on the function of the Autonomic System in patients after Myocardial Infarction or Stroke.
A secondary objective is to examine whether it is possible to predict which of the patients will most benefit from physical activity (exercise training), taking into account, genetic factors such as Polymorphism of ACE (Angiotensin Converting Enzyme)
| Condition | Intervention | Phase |
|---|---|---|
|
HR Vaiability, Aerobic Physical Fitness,Blood Pressure, Blood Sugar Level, Blood HDL, LDL |
Procedure: Aerobic exercise training |
Phase 1 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Intervention Model: Factorial Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | The Effect of Aerobic Exercise Training On the Function of the Autonomic System In Patients That Have Suffered Myocardial Infarction or Stroke |
- HR vriability at 12 weeks
- B.P., blood sugar level, tryglycerides, HDL, LDL, CRP and aerobic physical fitness,at 12 weeks.
| Estimated Enrollment: | 230 |
| Study Start Date: | January 2006 |
Show Detailed Description Eligibility| Ages Eligible for Study: | 20 Years to 80 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
Inclusion Criteria: The research subjects include a) patients after Myocardial Infarction between the ages 20 - 80 , who underwent percutaneous coronary interventions (PCI), and b) patients after a first Stroke between ages 20 - 80, up to two months after the stroke, with a NIH Stroke Score of 6 - 20 and who are able to cooperate and follow instructions.:
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Exclusion Criteria:1) Unstable Angina Pectoris2) Valvular Heart disease 3) Cardiomyopathy4) uncontrolled Hypertension.5) Cardiac Insufficiency (uncontrolled)6) uncontrolled arrhythmia 7) Severe Skeletal problems, or other physical, mental or medical problems liable to limit the patient' ability to participate.8) Incompliance.9) Patients who develop symptoms during the research, will be removed.
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Contacts and Locations| Contact: Ayelet Giladi, MSc | 00 972 3 9793424 | miron@hotmail.co.il |
| Contact: Isabella Schwartz, Dr | : 00 972 2 5844474 | Isabellas@hadassah.med.org |
| Israel | |
| Hadassah Medical Organization, Jerusalem, Israel | Not yet recruiting |
| Jerusalem, Israel | |
| Contact: Arik Tzukert, DMD :00 972 2 6776095 arik@hadassah.org.il | |
| Contact: IsabellaHadas Lemberg, PhD 00 972 2 6777572 lhadas@hadassah.org.il | |
| Sub-Investigator: Ayelet Giladi, Msc | |
| Principal Investigator: | Isabella Schwartz, Dr | Hadassah Medical Organization |
More Information
No publications provided
| ClinicalTrials.gov Identifier: | NCT00259948 History of Changes |
| Other Study ID Numbers: | Cva-mi-HMO-CTIL |
| Study First Received: | November 30, 2005 |
| Last Updated: | November 30, 2005 |
| Health Authority: | Israel: Israeli Health Ministry Pharmaceutical Administration |
Keywords provided by Hadassah Medical Organization:
|
HR variability, CVA, Myocardial infarction, aerobic exercise training |
Additional relevant MeSH terms:
|
Infarction Myocardial Infarction Ischemia Pathologic Processes Necrosis |
Myocardial Ischemia Heart Diseases Cardiovascular Diseases Vascular Diseases |
ClinicalTrials.gov processed this record on May 16, 2013