Actively Recruiting

Phase Not Applicable
Age: 18Years - 30Years
All Genders
Healthy Volunteers
ID06138106

Developing a Nutritional Supplement to Increase Collagen Synthesis in People

Led by University of California, Davis · Updated on 2026-01-30

20

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating whether a natural dietary supplement can enhance collagen production in healthy young adults aged 18 to 30 years. The study focuses on understanding if the supplement can increase collagen synthesis after consuming collagen protein, using a model that tests natural products certified as safe that stimulate collagen production in laboratory settings. The investigation aims to see how this supplement affects collagen synthesis in connective tissue with the support of exercise. Participants will be randomly assigned to one of two groups. One group will consume a supplement containing hydrolyzed collagen (20 grams) combined with vitamin C, epicatechin, vitamin E, and stevia extract. The other group will receive a placebo supplement with hydrolyzed collagen, vitamin C, and sweetener. Both groups will perform load-bearing exercise daily for 7 days while consuming their assigned supplement. Blood samples will be collected before and one hour after supplement intake, and also four hours after the final exercise session on day seven. During the study, researchers will analyze blood samples and treat engineered human ligaments with these serum samples to assess collagen production. They will measure collagen protein synthesis over 7 days, as well as the strength and collagen content of ligament constructs 60 minutes after exercise. Participants will be closely monitored throughout the trial, which is expected to last about one week. The study is conducted by the University of California, Davis, and includes healthy volunteers within the specified age range.

CONDITIONS

Brief Title

Developing a Nutritional Supplement to Increase Collagen Synthesis in People

Who Can Participate

Age: 18Years - 30Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Young healthy adults aged 18 to 30 years
Not Eligible

You will not qualify if you...

  • Pregnancy
  • Smoking
  • Receiving any medication that may interfere with the study outcomes

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - 7 days

Participants consume either the natural product supplement or placebo for 7 days while performing load-bearing exercise. Blood samples are collected before and one hour after consuming the supplement on the first day, and on the final day, blood is collected 4 hours after the exercise.

Daily supplement intake with blood draws on Day 1 and Day 7

Trial Site Locations

Total: 1 location

1

Hickey Laboratory

Davis, California, United States, 95616

Actively Recruiting

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Research Team

K

Kevin Paulussen, PhD

K

Keith Baar, PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

CROSSOVER

Primary Purpose

TREATMENT

Number of Arms

2

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