A Single-Group Clinical Trial to Evaluate the Effects of Health Nag's BioActive Collagen Jelly on Skin, Hair, Nail, and Joint Health

September 30, 2025 updated by: Nag Food Supplement Trading LLC
This decentralized, single-arm, open-label study evaluates the effects of Health Nag's BioActive Collagen Jelly on skin, hair, nail, and joint health in 40 female participants over 12 weeks. Participants will submit online questionnaires and standardized digital photos, which will be analyzed by dermatology experts.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Study Type

Interventional

Enrollment (Actual)

40

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • United States
    • Nevada
      • Las Vegas, Nevada, United States, 89118
        • Citruslabs

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Be female
  • Be aged 30-55.
  • Anyone who has concerns surrounding their skin health and appearance over the last four weeks.
  • Anyone who has concerns surrounding their hair health and hair fall or thinning over the last four weeks.
  • Anyone who has been using the same hair and skincare routine and products for at least one month prior to the study, i.e., shampoo, conditioner, products, cleanser, toner, and makeup remover.
  • Anyone willing to maintain the same hair and skincare routine and products throughout the 6-month trial, i.e., shampoo, conditioner, products, cleanser, toner, and makeup remover.
  • Is willing to discontinue any other supplements or herbal remedies that target skin or hair health including but not limited to collagen.
  • Anyone willing to avoid introducing any other supplements, medications, or herbal remedies for the duration of the trial.
  • Anyone who is generally healthy - does not live with any uncontrolled chronic disease.
  • Resides in the United States.
  • Not currently partaking in another research study and will not be partaking in any other research study for the next 6 months and at any point during this study's duration.
  • Anyone who owns a smartphone or camera.

Exclusion Criteria:

  • Anyone unwilling to follow the study protocol
  • Anyone who is planning to undergo facial treatments during the study period, including botox, dermal filler, chemical peels, etc.
  • Anyone who has undergone chemical treatments to the hair in the last three months e.g., chemical straightening, hair extensions with chemical bonding, perms, and relaxers.
  • Anyone with planned chemical treatments to the hair during the study period, e.g., chemical straightening, hair extensions with chemical bonding, perms, and relaxers.
  • Anyone currently taking any prescription medication for hair loss.
  • Anyone who has undergone any surgeries or invasive treatments in the last six months or is planning to undergo any surgeries or invasive treatments during the study.
  • Anyone who has had any major illness in the last three months.
  • Anyone who has any conditions that could affect the hair or scalp (e.g., alopecia areata)
  • Anyone who has stopped using hormonal birth control within the past month.
  • Anyone who has any chronic skin conditions on the face (e.g., eczema or psoriasis).
  • Anyone with pre-existing chronic conditions that would prevent participants from adhering to the protocol, including oncological and psychiatric disorders.
  • Anyone with any allergies or sensitivities to any of the study product ingredients.
  • Any women who are pregnant, breastfeeding, or trying to conceive (or who will be at any point during the study period).
  • Anyone who is vegan and/or does not consume animal products for any reason.
  • Anyone with a history of substance abuse.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: BioActive Collagen Jelly Intervention
Participants will consume 10 g of BioActive Collagen Jelly daily, on an empty stomach, for 12 weeks.
Dietary supplement: Dietary Supplement
The supplement is intended to support improvements in skin health, hair strength, nail strength, joint health, and overall well-being.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in Skin and Hair Health Assessed by Dermatologist Evaluation
Time Frame: Baseline to Week 12
Assessment of changes in skin and hair health from baseline to Week 12 based on standardized digital photographs evaluated by a dermatologist.
Baseline to Week 12

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in Participant-Reported Nail Strength, Joint Mobility, and Well-Being
Time Frame: Baseline, Week 2, Week 4, Week 8, and Week 12
Self-reported changes in nail strength, joint health, muscle recovery, and overall well-being measured via study-specific online questionnaires.
Baseline, Week 2, Week 4, Week 8, and Week 12

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Nag Food Supplement Trading LLC

Collaborators

Citruslabs

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

April 1, 2025

Primary Completion (Actual)

August 25, 2025

Study Completion (Actual)

August 25, 2025

Study Registration Dates

First Submitted

September 30, 2025

First Submitted That Met QC Criteria

September 30, 2025

First Posted (Estimated)

October 6, 2025

Study Record Updates

Last Update Posted (Estimated)

October 6, 2025

Last Update Submitted That Met QC Criteria

September 30, 2025

Last Verified

September 1, 2025

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 20743

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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