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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06019858
Other study ID # 20348
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date June 21, 2023
Est. completion date July 20, 2023

Study information

Verified date August 2023
Source Vitamin Energy®
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This is a virtual, single-arm clinical trial that will last 30 days. Participants will drink 1 bottle of the Vitamin Energy® shot daily and complete questionnaires at baseline, Day 7, Day 14, and Day 30. Participants' energy, mood, and cognitive function will be evaluated at baseline and at each check-in. Bodyweight will also be assessed at baseline and Day 30. Likert scale responses will be examined from baseline to each check-in. Participant responses on product feedback will be presented as % scores.


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date July 20, 2023
Est. primary completion date July 20, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: Men and women 18 years and over Self-reported issues with: - Energy - Focus - Brain fog Participants who often feel fatigued Willing to maintain the same caffeine consumption during the study period Generally healthy - don't live with any uncontrolled chronic disease Exclusion Criteria: Any pre-existing chronic conditions that would prevent participants from adhering to the protocol, including oncological and psychiatric disorders. Anyone with known severe allergic reactions. Women who are pregnant, breastfeeding, or attempting to become pregnant Unwilling to follow the study protocol.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Vitamin Energy Shot
Vitamin Energy® shot is a naturally-caffeinated functional energy shot that contains: Vitamin B3 Vitamin B6 Vitamin B12 Natural Caffeine (green tea extract) L-Carnitine Tartrate Potassium Sorbate Taurine Sucralose

Locations

Country Name City State
United States Citruslabs Santa Monica California

Sponsors (2)

Lead Sponsor Collaborator
Vitamin Energy® Citruslabs

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in energy levels. [Baseline to Day 30] Survey-based assessment (0-5 scale) of participant reported energy levels. 30 days
Secondary Change in ability to concentration. [Baseline to Day 30] Survey-based assessment (0-5 scale) of participant reported concentration abilities. 30 days
Secondary Change in participant-perceived productivity. [Baseline to Day 30] Survey-based assessment (0-5 scale) of participants perception of their productivity during the day. 30 days
Secondary Changes in mood. [Baseline to Day 30] Survey-based assessment (0-5 scale) of mood. 30 days
Secondary Changes in brain fog. [Baseline to Day 30] Survey-based assessment (0-5 scale) of brain fog experienced by participants. 30 days
Secondary Change in body weight. [Baseline to Day 30] Participants will weight themselves at baseline and endline and provide their body weight. 30 days
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