- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01199211
Impact of Physical Activity on Left Ventricular Mass and Lipid Metabolism
Impact of Physical Activity on Left Ventricular Mass and Lipid Metabolism in Healthy Female Volunteers Training for a Marathon
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Left ventricular hypertrophy, defined as an increase in the mass of the left ventricle may occur as a physiologic response to exercise (athletic remodeling aka "athletic heart"), but is most frequently encountered as a pathological manifestation of cardiovascular disease. The early determinants of athletic remodeling in the general population are largely unknown. In order to longitudinally explore the early determinants of athletic remodeling, we will recruit from the community, physically untrained women who have volunteered to run a marathon. We will prospectively assess left ventricular mass and function by echocardiogram during three consecutive stages/visits:
- Baseline: prior to starting intense physical training
- Trained: at the end of at least 12 week training period, prior to running the marathon.
- Post-marathon: 6 weeks after running the marathon.
In addition, exercise impacts lipid metabolism and short-term exercise is known to increase HDL levels in plasma. Human HDL is structurally heterogeneous, comprising at least sixteen discrete species. It has multiple functions, pertinent to cardiovascular medicine such as the ability to accept effluxed cholesterol from the artery wall, culminating in sterol uptake in the liver. This "reverse cholesterol transport pathway" is thought to prevent the accumulation of cholesterol in the artery wall. We will assess the clinical and genetic determinants of the HDL response to physical exercise.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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California
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San Francisco, California, United States, 94143
- CTSI - University of California San Francisco
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Healthy adult men or women, aged 18 years or older
- Voluntarily signed up for a sport event or to run a marathon or a half marathon for the first time
- Normal to mildly elevated blood pressure (systolic blood pressure < 140 mmHg and/or diastolic blood pressure < 90 mmHg)
- Hormone replacement therapy and birth control pills are allowed, provided they have been on a stable dose for more than 3 months and no change in dose is planned for the duration of the study
- Capable and willing to provide written, informed consent for the study
Exclusion Criteria:
- History of cardiovascular disease within the past year (cardiomyopathy, heart failure, ischemic heart disease, stroke, TIA, peripheral vascular disease)
- Change in body weight more than 10% over the past year
- History of significant medical conditions, including respiratory, gastrointestinal, neuromuscular, neurological or musculoskeletal problems interfering with exercise.
- Autoimmune or collagen vascular diseases, chronic anemia,
- Malignancies in the past 5 years, with the exception of treated skin or breast cancer that did not require treatment with chemotherapy.
- Diabetes
- Pregnancy or recent delivery: delivery date less than 3 months prior to enrollment
- Lipid lowering medications (statins, niacin, resins) are allowed, provided dose has not changed for 3 months prior to enrollment and is not anticipated to change during the study
- Fish Oil supplements are allowed, provided dose has been unchanged for 3 months prior to enrollment and no change in dose is planned for the duration of the study.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
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Exercise training, women, marathon.
Other: prospective study with no intervention
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Prospective study with no intervention in women who have volunteered to run a full marathon or a half-marathon.
Each subject will serve as own control.
Each subject will be studies at 3 stages: baseline, after at least 12 weeks of training for the marathon (we will not provide training), 6 weeks after running the marathon.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Lipid Metabolism
Time Frame: Baseline, In-Training, Post-training (at least 6 weeks after the race)
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Baseline, In-Training, Post-training (at least 6 weeks after the race)
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Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Heart architecture and function
Time Frame: Baseline, In-training, Post-training
|
Baseline, In-training, Post-training
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Collaborators and Investigators
Investigators
- Principal Investigator: Eveline Stock, MD, University of California, San Francisco
- Principal Investigator: Nelson Schiller, MD, University of California, San Francisco
Study record dates
Study Major Dates
Study Start
Primary Completion (ACTUAL)
Study Completion (ACTUAL)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ESTIMATE)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- CTSI-6212
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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Sohag UniversityNot yet recruitingLeft Ventricular Hypertrophy
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University of LeipzigCompletedLeft Ventricular Hypertrophy | Left Ventricular Failure | Left Ventricular Non-compaction CardiomyopathyGermany
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