A Clinical Study to Evaluate the Efficacy of Four Supplements on Improving Readiness for Intimacy

906 CMVI Holdings

Status: Active, not recruiting

Conditions: Gastrointestinal Issues; Libido; Intimacy

Treatments: Dietary Supplement: Stay Ready Fiber; Dietary Supplement: Libido; Dietary Supplement: Testosterone supplement; Dietary Supplement: Reset

Study type: Interventional

Funder types: Industry

Identifiers

NCT05862519

20287

Details and patient eligibility

About

This study is to evaluate the efficacy of four supplements designed to help participants get ready for sexual intimacy through improving digestion, weight management, sexual drive and stamina, and physical endurance during workouts and overall mood and quality of life. This study will be conducted as a single group, virtual trial, in which all participants will take all four supplements and complete online questionnaires. Participants will take the indicated supplements for the indicated amounts of time over 12 weeks. Questionnaires will be completed at baseline, and then at indicated times throughout the trial.

Enrollment: 36 patients

Sex: Male

Ages: 18 to 44 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Male (biological at birth) within the LGBTQIA+ community
• Aged between 18-44
• Generally healthy - don't live with any uncontrolled chronic disease
• Generally active lifestyle or seeking to achieve health improvement
• Sexually active with a partner

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.
• Unwilling to follow the study protocol.
• Currently experiencing significant symptoms of a mental disorder that might interfere with study participation (e.g. eating disorder, obsessive-compulsive disorder, posttraumatic stress syndrome, bipolar disorder)
• Current substance abuse disorder
• Diagnosis of an autoimmune disease, such as multiple sclerosis and rheumatoid arthritis
• Self-reported or diagnosed high blood pressure or hypotension (BP < 90 over 60)
• Currently, or in the past 6 months, undergoing hormone therapy
• Any medical condition that is unstable or uncontrolled
• A history of sexual trauma or abuse
• Has introduced any new prescription medication or supplements within the past 12 weeks that influence gastrointestinal issues, libido, or testosterone production.

Trial design

Primary purpose: Other

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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36 participants in 1 patient group

Intervention Group

Experimental group

Description:

Participants will begin taking the Reset supplement for 5 days. Then there will be a 2-day break with no products taken (wash out period). Participants will then begin taking the following 2 supplements: Stay Ready Fiber and libido with a partial overlap of products. Stay Ready Fiber will be taken from day 7 through 21, three capsules will be taken twice daily in the morning and afternoon. Libido will be taken from day 7 through 28, 2 capsules will be taken daily, preferably with a meal. Participants will then begin taking the Testosterone supplement. Testosterone will be taken from day 28 through to 84, 2 capsules will be taken daily, preferably with a meal.

Treatment:

Dietary Supplement: Reset

Dietary Supplement: Testosterone supplement

Dietary Supplement: Libido

Dietary Supplement: Stay Ready Fiber