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CompletedNCT07209137Updated Oct 6, 2025

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

An interventional study of Dietary Supplement in Joint Health, Hair Health and Skin Health, sponsored by Nag Food Supplement Trading LLC. Completed at 1 site in United States. Open to female participants aged 30 Years to 55 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-10-06.

Sponsored by Nag Food Supplement Trading LLC · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 5 months after the study started (first participant enrolled Apr 2025, registered Sep 2025).
Phase
Not applicable
Study type
Interventional
Enrollment
40
Allocation
Not applicable
Ages
30 Years to 55 Years
Sex
Female
01

Study summary

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.

02

Conditions studied

  • Joint Health
  • Hair Health
  • Skin Health

Keywords

  • Collagen Supplement
  • Muscle Recovery
03

In context

Lead sponsor

This is the only study on the registry with Nag Food Supplement Trading LLC as lead sponsor.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
30 Years to 55 Years
Sexes eligible
Female
Accepts healthy volunteers
Yes

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

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.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
40 participants (actual)

Study arms

  • 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

Interventions

  • Dietary supplementDietary Supplement

    The supplement is intended to support improvements in skin health, hair strength, nail strength, joint health, and overall well-being.

06

What researchers measure

Primary outcomes

  1. Change in Skin and Hair Health Assessed by Dermatologist Evaluation

    Assessment of changes in skin and hair health from baseline to Week 12 based on standardized digital photographs evaluated by a dermatologist.

    Time frame: Baseline to Week 12

Secondary outcomes

  1. Change in Participant-Reported Nail Strength, Joint Mobility, and Well-Being

    Self-reported changes in nail strength, joint health, muscle recovery, and overall well-being measured via study-specific online questionnaires.

    Time frame: Baseline, Week 2, Week 4, Week 8, and Week 12

07

Study locations

1 site
  • Citruslabs
    Las Vegas, Nevada 89118, United States
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 6, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07209137
Lead sponsor
Nag Food Supplement Trading LLC
Collaborators
Citruslabs
Responsible party
Sponsor
First posted
Oct 6, 2025
Start date
Apr 1, 2025
Primary completion
Aug 25, 2025
Completion
Aug 25, 2025
Last update
Oct 6, 2025

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Sep 2025. You cannot join it, but the record below documents what was studied.

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