Status:
COMPLETED
An Evaluation of the Effects of a Non-Caffeinated Energy Dietary Supplement
Lead Sponsor:
Nova Southeastern University
Conditions:
Health Behavior
Eligibility:
All Genders
18-50 years
Phase:
NA
Brief Summary
This study tested the effects of a botanical blend to a caffeine and a placebo condition on 1) self-reported alertness, anxiety, and headaches 2) multiple measures of attention 3) physical performance...
Detailed Description
This study aimed to build on this work by investigating the possibility that a specific botanical blend (Phytovive™); comprised of Bacopa monnieri bacosides, Kaempferia parviflora methoxy flavones, po...
Eligibility Criteria
Inclusion
- Adult males and females from 18 to 50 years (inclusive) of age who are physically active and have been engaging in athletic and sporting endeavors consistently over a period of 6 months at minimum
- BMI 18.0 (normal) to 34.9 (obese, class I) kg/ m2 inclusive
- Agrees to maintain a stable lifestyle with no change in exercise or diet for the duration of the study
- Current consumer of caffeine either through caffeinated beverages or foods
- Non-smoker
- Able to physically exercise, to run on a treadmill at moderate to high intensity for a brief time (typically less than 20 min)
- Participants with normal blood pressure or participants with hypertension that is controlled (BP \< 160/90 and who are on medication at a stable dose (same dose for ≥90 days)
- Willing and able to agree to the requirements and restrictions of this study, be willing to give voluntary consent, be able to understand and read the questionnaires, carry out all study-related procedures, communicate effectively with the study staff.
- Females must be using an acceptable method of contraception such as: abstinence, double barrier (condom, diaphragm, or cervical cap with spermicidal foam, gel, or cream), intrauterine device or hormonal contraception (oral, injectable, implantable, transdermal, or vaginal) used consecutively for at least 3 months prior to screening visit, vasectomized partner or use of implants for at least 6 months prior to screening visit; bilateral tubal ligation, hysterectomy, bilateral oophorectomy, or be postmenopausal status with amenorrhea (no menses) for at least 1 year prior to the screening visit.
Exclusion
- Have a known sensitivity or allergy to any of the study products or their ingredients
- Have any medical condition or disease based on the professional judgement and experience of the principal investigator (PI) plus research industry standards that might affect or impact the administration of study products
- Lactating, pregnant or planning to become pregnant during the study
- History of drug or alcohol abuse in the 12 months prior to screening
- History of psychiatric illness requiring hospitalization in the 6 months prior to screening
- History of diabetes (Type I or II) or uncontrolled hypertension (either systolic BP \>160 or diastolic BP \>90)
- Participation in or use of a research IP within 30 days prior to screening (cannot have been in another study within 30 days of screening)
Key Trial Info
Start Date :
January 3 2020
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
March 15 2021
Estimated Enrollment :
36 Patients enrolled
Trial Details
Trial ID
NCT04895800
Start Date
January 3 2020
End Date
March 15 2021
Last Update
June 9 2021
Active Locations (1)
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1
Nova Southeastern University
Davie, Florida, United States, 33314