NCT07756866

Brief Summary

This study evaluates the effects of Cowboy Colostrum bovine colostrum powder on gut health, body composition, hair growth, and skin appearance in generally healthy adults aged 21-47 with concerns in these areas. The trial is a single-arm, unblinded, virtual study conducted over 12 weeks in 35 participants who will use the test product daily. Participants will complete questionnaires and provide weight and waist circumference measurements at Baseline, Week 4, Week 8, and Week 12. The primary focus is on changes in weight and waist circumference, while secondary outcomes include participants' perceptions of gastrointestinal health, physical activity, hair growth, skin appearance, and overall health and well-being.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
35

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Jul 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

July 7, 2025

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 18, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

November 18, 2025

Completed
9 months until next milestone

First Submitted

Initial submission to the registry

August 5, 2026

Completed
6 days until next milestone

First Posted

Study publicly available on registry

August 11, 2026

Completed
Last Updated

August 11, 2026

Status Verified

August 1, 2026

Enrollment Period

4 months

First QC Date

August 5, 2026

Last Update Submit

August 5, 2026

Conditions

Outcome Measures

Primary Outcomes (2)

  • Change in Body Weight

    Self-reported body weight measured daily for three consecutive days at each time point using a Withings smart scale; the average of the two closest values is used

    Baseline, Week 4, Week 8, and Week 12

  • Change in Waist Circumference

    Self-reported waist circumference measured using a tape measure

    Baseline, Week 4, Week 8, and Week 12

Secondary Outcomes (13)

  • Change in Gastrointestinal Symptoms

    Baseline, Week 4, Week 8, and Week 12

  • Change in Digestion-associated Quality of Life

    Baseline, Week 4, Week 8, and Week 12

  • Change in Physical Activity

    Baseline, Week 4, Week 8, and Week 12

  • Participants' Perception of Bloating

    Baseline, Week 4, Week 8, and Week 12

  • Participants' Perception of Bowel Movement Frequency

    Baseline, Week 4, Week 8, and Week 12

  • +8 more secondary outcomes

Study Arms (1)

Cowboy Colostrum

EXPERIMENTAL
Dietary Supplement: Cowboy Colostrum

Interventions

Cowboy ColostrumDIETARY_SUPPLEMENT

All participants take two scoops of Cowboy Colostrum bovine colostrum powder daily (3.4 g serving containing 3 g bovine colostrum, organic Madagascar vanilla powder, monkfruit extract, and sea salt), either directly in the mouth or frothed into cold or warm liquids such as water, iced coffee, iced matcha, smoothies, yogurt, or oatmeal at any time of day for 12 weeks. The product must not be added to any liquid over 140 degrees.

Cowboy Colostrum

Eligibility Criteria

Age21 Years - 47 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Be male or female
  • Be aged 21-47
  • Anyone with concerns regarding all of the following over the past four weeks: gut health, healthy weight management, hair growth, and skin appearance
  • BMI 25-33 kg/m²
  • Anyone who is generally healthy and does not live with any uncontrolled chronic disease
  • Anyone who is physically active at least once per week
  • If taking any products, herbal remedies, over-the-counter medications, or supplements that target weight, gut health, physical activity, hair growth, or skin appearance, has been doing so consistently for three months and is willing to maintain this routine for the study duration
  • Willing to maintain their current diet and sleep schedule for the duration of the study
  • Willing to use the same skincare routine and make-up products for at least one month prior to the study, and willing to maintain this routine for the duration of the study
  • Resides in the United States

You may not qualify if:

  • Anyone with pre-existing chronic conditions that would prevent participants from adhering to the protocol, including oncological and psychiatric disorders
  • Anyone who has undergone any surgeries or invasive treatments in the last six months, or has any planned during the study period
  • Has had any major illness in the last three months
  • Anyone who has taken an antibiotic in the last three months
  • Anyone currently taking a weight loss medication, including but not limited to Wegovy, Mounjaro, and Ozempic
  • History of an autoimmune disorder, diabetes, or endocrine disorder
  • Food intolerances, allergies, or sensitivities such as dairy allergy and lactose intolerance
  • Has a known history of severe digestive disorders like acid reflux, Irritable Bowel Syndrome (IBS), Irritable Bowel Disease (IBD), Crohn's disease, or gastrointestinal tract surgeries
  • Anyone diagnosed with a skin or hair condition
  • Anyone who does not consume animal products for any reason
  • Currently undergoing hair treatment or using other hair growth/thickening products
  • Currently taking any prescription medication for hair loss
  • Anyone with any conditions that affect the hair or scalp (e.g., alopecia areata)
  • Anyone planning to undergo facial treatments during the study period, including Botox, dermal fillers, and chemical peels
  • Anyone with any allergies or sensitivities to any of the study product ingredients
  • +6 more criteria

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Citruslabs

Las Vegas, Nevada, 89101, United States

Location

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Sponsor Type
INDUSTRY
Responsible Party
SPONSOR

Study Record Dates

First Submitted

August 5, 2026

First Posted

August 11, 2026

Study Start

July 7, 2025

Primary Completion

November 18, 2025

Study Completion

November 18, 2025

Last Updated

August 11, 2026

Record last verified: 2026-08

Locations