Physical Performance Clinical Trial
Official title:
Effects of Increased Protein Intake and Exercise Training on Body Composition, Cardiovascular Health and Physical Performance
Verified date | October 2015 |
Source | Skidmore College |
Contact | n/a |
Is FDA regulated | No |
Health authority | United States: Institutional Review Board |
Study type | Interventional |
A primary aim of the current proposal is to compare the effect of daily consumption of healthy lean protein as either whey protein (2 meals per day) or whole food (25% of total daily caloric intake) consumed as 6 small meals throughout the day, one of which is consumed immediately following exercise training (within 30 min) and another 2 hours prior to going to bed at night, over a 16 week period on muscle and fat mass, cardiovascular health, aerobic fitness, glucose, insulin, blood lipids, heart rate and muscle strength in overweight men and women.
Status | Completed |
Enrollment | 25 |
Est. completion date | August 2013 |
Est. primary completion date | June 2011 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Both |
Age group | 30 Years to 60 Years |
Eligibility |
Inclusion Criteria: - Each participant was screened prior to participating in the study using the Health and Fitness History, Physical Activity, and Physical Activity Readiness questionnaires administered by the investigators. - Medical clearance was secured from the participant's primary care physician to verify no cardiovascular,metabolic or orthopedic issues that would prohibit them from performing the exercises for the duration of the study period - Depending on the outcome of the health history, fitness and activity questionnaires and the physician's clearance, participants were informed of eligibility to participate in the study. A group meeting was scheduled for all eligible and interested participants to review the entire study. This process took place prior to administering any tests. Exclusion Criteria: - Participants were excluded if they smoked, had a whey protein intolerance, or orthopedic conditions that prohibited them from engaging in strenuous exercise |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Skidmore College |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Cardiometabolic Hormones | Changes in plasma insulin levels | baseline and post 16 week intervention | No |
Other | Aerobic Fitness | Changes in oxygen consumption | baseline and post 12 week intervention | Yes |
Other | Hunger Ratings | Changes in hunger visual analog scale ratings | baseline and post 12 week intervention | No |
Other | Blood Lipids | Changes in total, LDL, HDL cholesterol | baseline and post 12 week intervention | No |
Other | Blood Pressure | Changes in systolic and diastolic blood pressure | baseline and post 12 week intervention | No |
Primary | Athletic Performance | Changes in one repetition maximum muscular strength of upper and lower body | baseline and post 16 week intervention | Yes |
Secondary | Total and Regional Body Composition | Changes in total and regional body fat assessed by dual energy xray | baseline and post 16 week intervention | No |
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