Actively Recruiting
30 Day Insulin Balance Metabolic Health Optimization Protocol
Led by Efforia, Inc · Updated on 2026-03-17
100
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
This research aims to explore how a dietary supplement called the Insulin Balance Formula may help support healthy insulin levels and its effects on weight, fatigue, and sugar cravings. The study focuses on generally healthy adults who want to maintain healthy insulin levels and improve overall metabolic health using this nutritional approach. It is an observational study where participants act as their own control in a single-arm design to detect initial signals of benefit and gather safety data. Participants will take the Insulin Balance Formula supplement daily for 30 days, starting with one capsule to assess tolerance and increasing to three capsules, ideally one before each meal or all at once. The formula contains five ingredients: Berberine, Beta Alanine, Zinc Citrate, Folate, and Fenugreek Extract. During the study, participants will follow a balanced diet and avoid introducing new supplements or health interventions. Throughout the 30-day period, participants will complete several assessments, including body composition measurement, the PROMIS Sleep Disturbance Scale, the Carbohydrate Craving Questionnaire, and evaluations of hunger and fatigue after meals. These will be done at baseline and study completion, with some hunger and fatigue assessments repeated randomly during the study. Participants are encouraged to provide honest feedback, and their privacy is protected. The study aims to generate meaningful data on how this supplement may support metabolic health and guide future research.
CONDITIONS
Brief Title
30 Day Insulin Balance Metabolic Health Optimization Protocol
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults 18 years or older who are generally healthy
- Ability to read and understand English
- Willingness and ability to provide informed consent and follow study procedures
You will not qualify if you...
- Known allergies
- Pregnant or nursing individuals
- Individuals with insulin disorders
- Individuals with gastrointestinal disorders
- Individuals with mental health conditions
- Individuals with sleep disorders
- Individuals currently on medication
- Athletes under specific regulations
- Individuals sensitive to fatigue
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 30 days
Participants take the Insulin Balance Supplement daily while following a balanced diet and complete assessments on body composition, sleep disturbance, carbohydrate cravings, and hunger & fatigue perception.
1 baseline visit and 1 visit at study completion with additional assessments repeated 6 times over 2 weeks
Trial Site Locations
Total: 1 location
1
Efforia
New York, New York, United States, 10003
Actively Recruiting
Research Team
M
Matthew Amsden
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
HEALTH_SERVICES_RESEARCH
Number of Arms
1
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