Hunger Perception and Weight-Related Outcomes Following Use of a Leptin-Supporting Dietary Supplement
Part of paid clinical trials in New York, New York.
- Sponsor
- Efforia, Inc
- Study ID
- NCT07442864
- Status
- Recruiting
Conditions
- Hunger
- Weight Change
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Accepted
Interventions
- Leptin Balance Formula — DIETARY_SUPPLEMENTParticipants will self-administer the Leptin Balance Formula daily for 12 weeks according to product labeling. The supplement is commercially available and includes African mango seed extract, chromium picolinate, Ceylon cinnamon, and alpha lipoic acid.
Study Details
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 Dates
- Start date
- Sep 10, 2025
- Status verified
- Sep 2025
- Primary completion
- Sep 10, 2026
- Completion
- Sep 10, 2026
Study Design
- Enrollment
- 100 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- HEALTH_SERVICES_RESEARCH
Arms
- Experimental: Single Arm longitudinal where participants act as their own controlSingle Arm longitudinal where participants act as their own control
Primary Outcome Measure
Change in Hunger Perception [ Time Frame: Baseline and Week 12 ]
Central Contacts
- Matthew Amsden646-679-2479
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Efforia | New York | New York | 10003 |
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