Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Pharmanex
With
University of North Carolina, Chapel Hill
Age
25–50
Sex
ALL
Healthy volunteers
Accepted
You may be eligible if
Participant is an adult between the ages of 25-50 years
Participant has a recorded BMI of 20-35 kg/m2
Participant exercises less than 3 hours per week for at least 8 weeks preceding the study
Participant has provided written and dated informed consent to participate in the study
Participant is willing to and able to comply with the protocol
Participant is apparently healthy and no reported metabolic disorders, heart disease, arrhythmias, thyroid disease, renal, hepatic, autoimmune or neurological diseases, as determined by a health history questionnaire
Participant agrees to maintain current diet and exercise routine during the study
Participant agrees to refrain from taking any anti-inflammatory supplement 48 hours prior to exercise or for exercise related pain or medications to prevent any further nutritional or drug related protection against exercise induced muscle damage
Participant agrees to wear an accelerometer to track activity during entire study
Participant has a resting (seated for 5 minutes) blood pressure of systolic pressure between 140-90 mmHg and a diastolic pressure between 90-50 mmHg
You may not be if
Participant is currently enrolled in a separate clinical trial or weight loss program involving diet, exercise, physical activity, or the potential ingestion of an active drug or dietary supplement Participant is using, or has consistently used one of the following dietary supplements within 12 weeks prior to enrollment: Beta-alanine, Creatine, HMB, Carnosine, Vitamin D
Participant has consistently consumed whey protein/plant protein and/or 1,000 mg of fish oil within the previous 4 weeks prior to enrollment
Participant has gained or lost ≥ 8 lbs in the previous month
Participant has a known allergy or sensitivity to the placebo or active ingredients
Participant has used tobacco more than three days per week (on average) in the previous 6 months, or refuses to abstain from all tobacco use for the duration of the study
Participant is pregnant or planning to become pregnant
Participant has any musculoskeletal condition prohibiting them from participation
