A Clinical Trial to Evaluate the Effects of a Herbal Tincture on Energy Levels, Weight Management, and Markers of Metabolic Health

Apothekary

Status: Active, not recruiting

Conditions: Fatigue; Stress

Treatments: Dietary Supplement: Blue Burn Tincture

Study type: Interventional

Funder types: Industry

Identifiers

NCT06949540

20716

Details and patient eligibility

About

This study will evaluate the effects of the Blue Burn Tincture on energy levels, weight management, and markers of metabolic health. It is a single-arm, hybrid trial involving 40 participants over a 12-week period. Participants will use the product daily, complete scheduled questionnaires, attend blood tests at Labcorp (Baseline and Week 12), and provide body mass measurements. Primary outcomes include changes in cortisol levels, energy levels, and body mass.

Enrollment: 40 estimated patients

Sex: All

Ages: 30+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Be male or female.

• Be aged 30 or over.

• Anyone who owns a body weight scale.

• Anyone currently experiencing issues regarding all of the following:

  1. Self-reported feelings of stress.
  2. Self-reported issues with maintaining their current body weight or losing weight.

• Exercises at least once per week.

• If taking prescription medications, are willing to discuss this study with their physician before starting the study.

• Willing to maintain the study protocol for the study duration.

• Willing to refrain from taking any products, new medication, or supplements that target cortisol levels, stress, energy levels, or weight management during the study duration.

• If taking oral over-the-counter supplements or herbal remedies targeted at improving cortisol levels, stress, energy levels, or weight management, has been consistently taking these for at least 3 months prior to starting the study and is willing to maintain this routine for the study duration.

• Willing to maintain their current diet, sleep schedule, and activity level for the study duration.

• Anyone who is generally healthy - does not live with any uncontrolled chronic disease.

• Resides in the United States.

• Not currently partaking in another research study and will not be partaking in any other research study for the next 12 weeks and at any point during this study's duration.

Exclusion criteria

• Anyone with pre-existing chronic conditions that would prevent participants from adhering to the protocol, including oncological and psychiatric disorders.
• Anyone who is planning to undergo any surgeries or invasive treatments for the study duration.
• Anyone diagnosed with a condition related to the thyroid.
• Anyone diagnosed with Type I or Type II diabetes.
• Anyone who has had any major illness in the last three months.
• Anyone who drinks heavily (i.e., eight or more alcoholic drinks per week for women or 15 or more alcoholic drinks per week for men).
• Anyone with an allergy to nightshade vegetables.
• Anyone with known severe allergic reactions to any of the study product ingredients.
• Any women who are pregnant, breastfeeding, or trying to conceive (or who will be at any point during the study period).
• Anyone with a history of substance abuse.
• Anyone who is currently a smoker or has been a smoker in the past 3 months.

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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40 participants in 1 patient group

Blue Burn Tincture Group

Experimental group

Description:

Participants will receive 4 mL of the Blue Burn Tincture daily for 12 weeks. The dose is split into 2 mL in the morning and 2 mL at lunchtime (before 2 PM), mixed with water or another liquid.

Treatment:

Dietary Supplement: Blue Burn Tincture