Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
George Washington University
Age
20–40
Sex
ALL
Healthy volunteers
Accepted
You may be eligible if
Males or females between the ages of 20 and 40 years
A body mass index (BMI) of 20.0 - 29.9 kg/m2.
Low risk for risk of injury or health complications as determined by physical activity readiness questionnaire (PARQ).
You may not be if
Are currently taking any antioxidant supplementation (daily multivitamin not included), prescribed non-steroidal anti-inflammatory drugs (NSAIDS), antibiotics, steroids, or probiotics.
Are currently taking any medications for management of cholesterol, diabetes, or body weight/obesity, or are undergoing hormone therapy.
Are unwilling or unable to comply with study procedures, at the discretion of the investigators.
Are unwilling to have biospecimens (blood and urine) collected and stored (only blood) for future research.
Pregnant women - A urine pregnancy test will be conducted prior to any testing procedures.
A history of disordered eating, including anorexia nervosa, bulimia nervosa, binge eating disorder, or avoidant restrictive food intake disorder or deemed high-risk for disordered eating via questionnaire.
A history of gastrointestinal diseases, such as galactosemia, gastroesophageal reflux disease (GERD), irritable bowel syndrome (IBS), Celiac disease, Crohn's disease, or lactose intolerance.
Individuals with known allergies to wheat or gluten, milk, soy, tree nuts (e.g., almonds, walnuts, pecans), or peanuts.
Deemed high risk for food insecurity via the Hunger Vital Sign screener.
Have followed a ketogenic diet within the last three months or have been told to avoid a high-fat diet by a medical provider for risk of cardiovascular disease.
Cardiorespiratory fitness (VO2max) below the 30th percentile for age and sex (measured at initial screening visit)
Clareo Health | Protective Effect of Exercise on Acute High-fat Overfeeding
