Hunger Perception and Weight-Related Outcomes Following Use of a Leptin-Supporting Dietary Supplement

Recruiting now · Not applicable

Conditions studied: Hunger, Weight Change

In brief

This study evaluates changes in hunger perception and body composition-related measures following daily use of a commercially available dietary supplement formulated to support leptin-related metabolic signaling. Adult participants will self-administer the supplement for 12 weeks and complete periodic self-reported assessments related to appetite, hunger, and weight-related outcomes. Participants serve as their own control, with comparisons made between baseline and follow-up measurements. The study is designed to generate preliminary, real-world evidence regarding supplement use in a general wellness context.

Key facts

Study ID

NCT07442864

Run by

Efforia, Inc

People needed

100

Starts

2025-09-10

Expected to finish

2026-09-10

Last updated by the study team

2026-03-02

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Adults aged 18 years or older
• Willing to pay for study supplies and able to take the dietary supplement daily for 12 weeks
• Willing to complete electronic questionnaires and self-reported measurements
• Able to provide informed consent

You may not qualify if…

• Pregnant or breastfeeding individuals
• Known allergy or sensitivity to any supplement ingredients
• Use of medications or supplements that could interfere with appetite or weight without medical clearance
• Any medical condition that would make participation unsafe, as determined by the participant

Where it is running

• Efforia — New York, New York, United States (enrolling)

Full record on ClinicalTrials.gov

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