Comparing the effects of bovine and marine collagen on skin, hair, nails, and overall health
BECOME Study: Comparative Efficacy of Bovine and Marine Collagen Versus Placebo on Skin, Hair, Nails and Whole Body Health Markers
This study is testing whether taking bovine or marine collagen supplements can improve skin, hair, nails, and overall health in healthy women aged 35-55.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 90 (estimated) |
| Ages | 35 Years to 55 Years |
| Sex | Female |
| Sponsor | Ancient + Brave Industry-sponsored |
| Locations | 1 site (Chelmsford, Essex) |
| Trial ID | NCT06603194 on ClinicalTrials.gov |
What this trial studies
The BECOME Study evaluates the effectiveness of bovine and marine collagen supplements compared to a placebo in improving skin, hair, nails, and overall health in healthy adults. This randomized controlled trial will assess various health parameters, including skin elasticity and joint health, over a specified period. Participants will be women aged 35-55 who are comfortable with the collagen sources being tested. The study aims to determine which collagen source is more effective for enhancing health outcomes.
Who should consider this trial
Good fit: Ideal candidates are healthy females aged 35-55 who are comfortable with bovine or marine collagen.
Not a fit: Patients who are pregnant, breastfeeding, or have chronic skin conditions may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide insights into the most effective collagen source for improving skin, hair, and nail health.
How similar studies have performed: Other studies have explored collagen supplementation, but this specific comparison of bovine versus marine collagen is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: Females aged 35-55 years. Participants must be comfortable with bovine or marine collagen (non-vegan/vegetarian). Must provide informed consent and be willing to comply with study requirements. Exclusion Criteria: Pregnant or breastfeeding women. History of chronic skin conditions (e.g., eczema, psoriasis) that might interfere with study outcomes. Any active skin infections or severe acne. Currently taking collagen supplements or have taken them within the last 6 months. Use of medications or topical agents that can affect skin, hair, nails, or gastrointestinal health (e.g., corticosteroids, retinoids). Excessive alcohol consumption or current smokers. Regular use of sunbeds. Recent cosmetic procedures (e.g., Botox, fillers, chemical peels, laser treatments) on skin, hair, or nails within the last 3 months. Any condition or situation that, in the opinion of the investigator, may interfere with the participant's ability to comply with the study requirements or give informed consent. Poor adherence to previous study protocols
Where this trial is running
Chelmsford, Essex
- Princeton Consumer Research, 8 Richmond Road, Dukes Park — Chelmsford, Essex, United Kingdom (Recruiting)
Study contacts
- Principal investigator: Jenna Macciochi, PhD — jenna@ancientandbrave.earth
- Study coordinator: Jenna Macciochi, PhD
- Email: jenna@ancientandbrave.earth
- Phone: +447799090189
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.