Egg Cholesterol Consumption, Blood Cholesterol and Skeletal Muscle Hypertrophy
NCT ID: NCT00260442
Last Updated: 2025-09-29
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
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
36 participants
INTERVENTIONAL
2005-11-30
2018-01-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Effects of Increased, Egg-Based Protein Intake on Muscle Composition,
NCT01396915
Effectiveness of Egg Versus Whey Protein Powder During Resistance Training
NCT05206253
Supplemental Egg Protein Intervention in Older Adults
NCT03530774
Protein Intake and Step Reduction in Older Adults
NCT03285737
Egg Consumption and Muscular Adaptations
NCT04381390
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
The secondary objective of this proposal is to test the hypothesis that increased dietary cholesterol consumption in the context of an exercise program does not alter blood cholesterol concentrations or other cardiovascular risk factors.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
PREVENTION
QUADRUPLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Placebo
\< 200 mg/day dietary cholesterol, resistance training, sedentary
Resistance Training
12 weeks, 3 times a week whole body resistance training
Sedentary
Absence of physical activity
Average intake
400 mg/day dietary cholesterol, resistance training, sedentary
Resistance Training
12 weeks, 3 times a week whole body resistance training
Sedentary
Absence of physical activity
High intake
800 mg/day dietary cholesterol, resistance training, sedentary
Resistance Training
12 weeks, 3 times a week whole body resistance training
Sedentary
Absence of physical activity
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Resistance Training
12 weeks, 3 times a week whole body resistance training
Sedentary
Absence of physical activity
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* able to perform exercise testing and training
Exclusion Criteria
* cardiac arrhythmias
* cancer
* hernia
* aortic aneurysm
* kidney disease
* lung disease
* total cholesterol \> 240 mg/dl or \< 160 mg/dl
* current use of cholesterol lowering medications
* actively participating in \>1 hour per week of resistance training
50 Years
69 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Texas A&M University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Steven E.Riechman, PhD, MPH
Associate Professor
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Steven E Riechman, PhD, MPH
Role: PRINCIPAL_INVESTIGATOR
Texas A&M University
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Texas A&M University
College Station, Texas, United States
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
481031-001-CA
Identifier Type: -
Identifier Source: secondary_id
0600083
Identifier Type: -
Identifier Source: secondary_id
06-0187
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.