- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05858476
An Investigation Into a 21-Day Detoxification Diet With a Seven-Day Continuation
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
California
-
Santa Monica, California, United States, 09404
- Citruslabs
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Must be in good general health with no chronic health conditions
- BMI under 35.
- Must own a scale at home.
- Must experience at least one of the following issues: the feeling of being tired at least several times a week, brain fog, sleep issues, trouble with focus and concentration, or having a busy, stressful life.
- A subgroup of 10 study participants must be diagnosed with T2D for ≥ 90 days, with an hbA1c of 7.5 to 10.5, inclusive
- Eat fast food at least twice a week.
- Does not exercise regularly.
- Does not consume fruits and vegetables daily.
- Must experience at least one of the following gastrointestinal problems: often bloating, excessive gas, heartburn, and irregular bowel movements.
- Must experience at least one of the following aches regularly: body aches, joint pain, back pain, or neck pain.
- Must be willing to go to Quest labs for two blood draws, one at baseline and the other at the study's conclusion.
- Willing to avoid bottled water for the duration of the study.
Exclusion Criteria:
- Suffers from pre-existing conditions that prevent them from adhering to the protocol.
- Anyone with known severe allergic reactions.
- Currently pregnant, breastfeeding, or wanting to become pregnant for the duration of the study.
- Anyone unwilling to use the test product daily as directed.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Chef V's 21-Day Starter Challenge Detox & Green Drink Supplement
The detox program provides the three primary macronutrients alongside antioxidants to promote detoxification. The 21-Day Detox schedule is below: Days 1-7: Healthy Routine- The Healthy Routine involves drinking a 16oz Green Drink and Protein Shake for breakfast and then choosing their lunch, snack, and dinner from the Meal Planner that will be provided. Days 8-10: 3-Day Cleanse- Each day during the three-day cleanse, participants will consume 4 16oz Green Drinks, 2 Protein Shakes, and a Soup designed explicitly to detox the body. Days 11-21: Healthy Routine- The last period of the 21 days will mimic the Healthy Routine from Days 1-7. Days 21-28 Participants will follow up this program by using the Green Drink supplement provided for an additional 7 days. |
Detox plan description: 7AM Water 16oz. 8AM Green Drink 16oz. 9AM Ultra Shake 16oz. 9-12PM Water 24 - 48oz. 12PM Green Drink 16oz. 12:30 - 2PM Water 24 - 48oz. 2PM Green Drink 16oz. 3PM Ultra Shake 16oz. 3:30- 6PM Water 24 - 48oz. 6PM Green Drink 16oz. 7PM Detox Soup 16oz. 7:30 - 10PM Water 24 - 48oz. This 21-day period will be followed by 7 days of consuming the Green Drink Supplement. |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Changes in participant perceptions of well-being [Time Frame: Baseline to 28 days)
Time Frame: 28 days
|
Survey-based assessment (0-5 scale) of changes in IBS symptoms).
Participants will answer surveys at the study baseline, and on Days 5, 11, 21 and 28 of the trial.
|
28 days
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in hs-CRP [Time Frame: Baseline to 28 days]
Time Frame: 28 days
|
Blood draws will be taken at Baseline and Day 28 for comparison.
|
28 days
|
|
Change in blood lipid profile [Time Frame: Baseline to 28 days]
Time Frame: 28 days
|
Blood draws will be taken at Baseline and Day 28 for comparison.
|
28 days
|
|
Change in HbA1C [Time Frame: Baseline to 28 days]
Time Frame: 28 days
|
Blood draws will be taken at Baseline and Day 28 for comparison.
|
28 days
|
|
Change in bodyweight [Time Frame: Baseline to 28 days]
Time Frame: 28 days
|
Weight will be measured using an electric scales at the study baseline and on Days 3, 5, 14, and 18.
|
28 days
|
Collaborators and Investigators
Sponsor
Collaborators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 20267
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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