Fatigue Clinical Trial
Official title:
A Clinical Trial to Assess the Effects of a Vitamin Shot on Energy Levels
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 |
Verified date | August 2023 |
Source | Vitamin Energy® |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
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.
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. |
Country | Name | City | State |
---|---|---|---|
United States | Citruslabs | Santa Monica | California |
Lead Sponsor | Collaborator |
---|---|
Vitamin Energy® | Citruslabs |
United States,
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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