Hair Thinning, Nails, Skin Laxity
Conditions
Keywords
Collagen, Skin health, Skin density
Brief summary
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.
Interventions
DIETARY_SUPPLEMENTBovine or Marine Collagen
Bovine or Marine Collagen
Sponsors
Princeton Consumer Research
Ancient + Brave
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Investigator)
Eligibility
Sex/Gender
FEMALE
Age
35 Years to 55 Years
Healthy volunteers
Yes
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
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Changes in skin hydration | Baseline, week 6 and week 12 | Changes in skin hydration will be assessed by a Corneometer |
| Change in skin wrinkles | Baseline, week 6 and week 12 | Measurement of the reduction in skin wrinkles using Profilometer |
| Changes in skin pigmentation | Baseline, week 6 and week 12 | Changes in skin pigmentation will be assessed by Chromameter |
| Change in perceived skin health | Baseline, week 6 and week 12 | Changes in perceived skin health assessed by self perception questionnaire |
| Change in skin wrinkles by visual assessment | Baseline, week 6 and week 12 | Change in skin wrinkles will be performed by visual assessment by a dermatologist |
| Change in nail strength and growth | Baseline, week 6 and week 12 | Assessment of nail strength and growth will be assessed by self-perception questionnaire |
| Change in skin elasticity | Baseline, week 6 and week 12 | Changes in skin elasticity will be measured by a cutometer |
| Change in hair thickness and strength | Baseline, week 6 and week 12 | Strength and breakage of hair will be assessed by self perception questionnaire |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Subjective Perception Questionnaire | Baseline, week 6 and week 12 | Subjective Perception Questionnaire (SPQ) for Whole Body Health to capture participants' self-reported perceptions of their overall health and well-being |
| Digestive Quality of Life (DQDL) Assessment | Baseline, week 6 and week 12 | Participants will complete a Digestive Quality of Life (DQDL) Assessment to evaluate the digestive health benefits |
Countries
United Kingdom
Contacts
Primary ContactJenna Macciochi, PhD
Backup ContactBecky Clarke
Outcome results
None listed