Actively Recruiting

Phase Not Applicable
Age: 35Years - 55Years
FEMALE
Healthy Volunteers
NCT06603194

Benefit of Bovine or Marine Collagen Vs. Placebo on Skin, Hair, Nails and Whole Body Health in Healthy Adults

Led by Ancient + Brave · Updated on 2024-09-19

90

Participants Needed

1

Research Sites

16 weeks

Total Duration

On this page

Sponsors

A

Ancient + Brave

Lead Sponsor

P

Princeton Consumer Research

Collaborating Sponsor

AI-Summary

What this Trial Is About

The BECOME Study (Bovine and Marine Collagen Efficacy for Skin, Hair, Nails and Whole Body Health Markers Evaluation) is a randomized controlled trial designed to compare the effects of bovine and marine collagen supplements versus a placebo on skin, hair, nails and whole body health markers. The trial aims to determine the most efficacious collagen source for improving health outcomes and to establish if both types of collagen are equally effective. Participants will be assessed on various health parameters, including skin elasticity, joint health, digestive health, and overall well-being, over a specified period.

CONDITIONS

Official Title

Benefit of Bovine or Marine Collagen Vs. Placebo on Skin, Hair, Nails and Whole Body Health in Healthy Adults

Who Can Participate

Age: 35Years - 55Years
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Female aged 35 to 55 years
  • Comfortable with bovine or marine collagen (non-vegan/vegetarian)
  • Provide informed consent and willing to follow study requirements
Not Eligible

You will not qualify if you...

  • Pregnant or breastfeeding women
  • History of chronic skin conditions such as eczema or psoriasis
  • Active skin infections or severe acne
  • Currently taking or taken collagen supplements within the last 6 months
  • Use of medications or topical agents affecting skin, hair, nails, or digestive health (e.g., corticosteroids, retinoids)
  • Excessive alcohol consumption or current smoker
  • Regular use of sunbeds
  • Recent cosmetic procedures on skin, hair, or nails within the last 3 months (e.g., Botox, fillers, chemical peels, laser treatments)
  • Any condition that may interfere with study compliance or informed consent
  • Poor adherence to previous study protocols

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Princeton Consumer Research, 8 Richmond Road, Dukes Park

Chelmsford, Essex, United Kingdom, CM2 6UA

Actively Recruiting

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Research Team

J

Jenna Macciochi, PhD

CONTACT

B

Becky Clarke

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

3

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