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OpenTrials
Completed

NCT Number: NCT06019858

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

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.

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Key information

Conditions

Energy Body Weight Body Weight Changes Cognition Fatigue Mood Pathological Conditions, Signs and Symptoms Signs and Symptoms Weight Loss

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Citruslabs

Santa Monica, California, 90404, United States

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Vitamin Energy Shot

Other

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

Primary outcomes

  1. Change in energy levels. [Baseline to Day 30]

    Time frame: 30 days

    Survey-based assessment (0-5 scale) of participant reported energy levels.

Secondary outcomes

  1. Change in ability to concentration. [Baseline to Day 30]

    Time frame: 30 days

    Survey-based assessment (0-5 scale) of participant reported concentration abilities.

  2. Change in participant-perceived productivity. [Baseline to Day 30]

    Time frame: 30 days

    Survey-based assessment (0-5 scale) of participants perception of their productivity during the day.

  3. Changes in mood. [Baseline to Day 30]

    Time frame: 30 days

    Survey-based assessment (0-5 scale) of mood.

  4. Changes in brain fog. [Baseline to Day 30]

    Time frame: 30 days

    Survey-based assessment (0-5 scale) of brain fog experienced by participants.

  5. Change in body weight. [Baseline to Day 30]

    Time frame: 30 days

    Participants will weight themselves at baseline and endline and provide their body weight.

Sponsors and collaborators

Lead sponsor

Vitamin Energy®

Industry

Collaborators

  • Citruslabs

Registry information

Important dates

Study start
2023
Primary completion
2023
Study completion
2023
First posted
Aug 31, 2023
Registry last updated
Aug 31, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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