Actively Recruiting

Phase Not Applicable
Age: 30Years - 60Years
FEMALE
Healthy Volunteers
NCT07526571

GLOW Study: Effects of Triple Protein in Women

Led by University of North Carolina, Chapel Hill · Updated on 2026-04-13

40

Participants Needed

1

Research Sites

34 weeks

Total Duration

On this page

Sponsors

U

University of North Carolina, Chapel Hill

Lead Sponsor

P

Perelel Inc.

Collaborating Sponsor

AI-Summary

What this Trial Is About

This single-site, randomized, blinded, placebo-controlled study will evaluate whether 4 weeks of daily Triple Support Protein powder improves glycemic control and overall well-being in healthy women aged 30-60 years. Participants will undergo baseline testing (DXA, fasting blood, standardized meal test with 2-hour glucose and insulin sampling), complete one acute supervised dose, and then consume a daily supplement for 4 weeks. During the final 14 days, participants will wear a continuous glucose monitor. Outcomes include postprandial glucose AUC, insulin sensitivity, and body composition.

CONDITIONS

Official Title

GLOW Study: Effects of Triple Protein in Women

Who Can Participate

Age: 30Years - 60Years
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Female aged 30 to 60 years
  • Body mass index (BMI) between 18.5 and 40 kg/m2
  • Recreationally active with at least 30 minutes of moderate intensity exercise per week
  • Healthy and free from disease based on health history questionnaire
  • Willing to avoid caffeine, tobacco, and alcohol for 24 hours before testing days
Not Eligible

You will not qualify if you...

  • Currently taking whey protein supplements
  • Pregnant or nursing
  • Lactose intolerant
  • Currently using creatine monohydrate
  • Severe hearing or speech impairment or unable to speak English

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Department of Exercise and Sport Science, Applied Physiology Laboratory

Chapel Hill, North Carolina, United States, 27713

Actively Recruiting

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Research Team

A

Abbie Smith-Ryan

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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