Effects of a Vitality Dietary Supplement on Physical and Mental Function in Middle-aged Adults

Pharmanex

Status

Completed

Conditions

Health-related Quality of Life

Treatments

Dietary Supplement: Vitality Product

Dietary Supplement: Placebo

Study type

Interventional

Funder types

Other

Industry

Identifiers

NCT01155076

10-SUS-03-NU-01

Details and patient eligibility

About

The purpose of the study is to determine the effects of 8 weeks Vitality Product supplementation on physical and mental function in middle-aged adults

Enrollment

116 patients

Sex

All

Ages

40 to 70 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Males and females aged 40-70 years
Signed Informed Consent
BMI between 19 and 30 kg/m2
Normotensive, defined as systolic blood pressure 90-140 mmHg and diastolic blood pressure 50-90 mmHg

Exclusion criteria

Regular dietary supplement use and unwilling to discontinue use at least 1 month prior to enrollment in the study
Self-reported chronic condition that may affect subject safety (e.g. diabetes, cardiovascular disease) or significantly impact product effectiveness (e.g. chronic fatigue)
Pregnancy/suspected pregnancy, breastfeeding
Antihypertensive medication use
Allergies to any supplement ingredients
Consumption of more than 600mg caffeine from any source per day
Consumption of "energy drinks" (e.g. Red Bull, Monster) or any herbal supplement known to affect energy levels
Known iron anemia
Medically treated for insomnia
Medically treated for depression
Taking medications known to affect energy, e.g. thyroid medication
Tobacco user
Planned surgical procedure in next 2 months
Participating in another clinical (medical or nutritional) study or likely to enroll in another medical or nutritional study