Gastrointestinal Issues, Intimacy, Libido
Conditions
Brief summary
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.
Interventions
DIETARY_SUPPLEMENTReset
Pure for Men Reset is a Vegan, Proprietary Blend of Toxin Eliminating Cleanser: Cascara Sagrada Bark, Senna Leaf, Psyllium Husk, Licorice Root, and Aloe Vera Gel. Taken on Day 1 to Day 5.
DIETARY_SUPPLEMENTStay Ready Fiber
Stay Ready Fiber is a Vegan, 100% Natural, Proprietary Blend of Digestive Aids: Psyllium Husk, Aloe Vera Extract, Chia Seeds & Flaxseed. Taken from Day 7 through Day 21.
DIETARY_SUPPLEMENTLibido
Supplement designed to support endurance and increased arousal. Contains L-Citrulline, L-Arginine and Black Pepper Fruit Extract (Piper Nigrum). Taken from Day 7 through to Day 28.
DIETARY_SUPPLEMENTTestosterone supplement
Supplement designed to enhance testosterone production. Contains Ashwagandha, Zinc, Vitamin D, Maca, and Tongkat Ali. Taken from Day 28 through Day 84.
Sponsors
Citruslabs
906 CMVI Holdings
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE
Eligibility
Sex/Gender
MALE
Age
18 Years to 44 Years
Healthy volunteers
Yes
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.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Changes in subject's perception of readiness and confidence for intimacy, and sex drive/arousal [Time Frame: Baseline to 12 weeks] | 12 weeks | Survey-based assessment (0-5 scale) of changes in reduction in preparation time for intimacy, sexual arousal, and sexual endurance. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Changes in digestion, stamina and endurance during workouts, overall confidence, mood and quality of life [Time Frame: Baseline to 12 weeks] | 12 weeks | Survey-based assessment (0-5 scale) of changes in digestion, stamina and endurance during workouts, overall confidence, mood and quality of life. |
Countries
United States
Outcome results
None listed