A Clinical Trial to Assess the Effects of a Vitamin Shot on Energy Levels

Not Applicable

Completed

• Conditions: Weight Loss; Fatigue; Cognition; Energy; Mood
• Interventions: Other: Vitamin Energy Shot

• Registration Number: NCT06019858
• Lead Sponsor: Vitamin Energy®

Brief 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.

Detailed Description

Not available

Study Timeline

• Study Start: 2023-06-21
• Primary Completion: 2023-07-20
• Study Completion: 2023-07-20
• Status Verified: 2023-08
• Study First Submitted: 2023-08-24
• Study First Submitted QC: 2023-08-24
• Last Update Submitted: 2023-08-24
• Study First Posted: 2023-08-31
• Last Update Posted: 2023-08-31

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 30

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

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Vitamin Energy Shot	Vitamin Energy Shot	Participants will take one bottle daily of the Vitamin Energy® shot, in the morning.

Primary Outcome Measures

Name	Time	Method
Change in energy levels. [Baseline to Day 30]	30 days	Survey-based assessment (0-5 scale) of participant reported energy levels.

Secondary Outcome Measures

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

Trial Locations

Locations (1)

Citruslabs; 🇺🇸 Santa Monica, California, United States