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

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorEfforia, Inc

About this trial

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.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

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

Disqualifiers

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

Trial design

Design model

Single group

Treatments tested in this trial

  • Leptin Balance Formula

    Dietary supplement

    Participants 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.

Treatment groups

100 Participants
are divided into 1 treatment group
Group A: Single Arm longitudinal where participants act as their own controlExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Change in Hunger Perception

Change from baseline in self-reported hunger perception as measured by a standardized hunger perception questionnaire.

Time frame
Baseline and Week 12

Secondary outcomes

1

Change in Body Weight

Self-reported body weight change from baseline.

Time frame
Baseline and Week 12
2

After-Meal Hunger and Fatigue Perception

Self-reported hunger and fatigue levels following meals using a structured questionnaire.

Time frame
Baseline, Week 4, Week 8, and Week 12

Other outcomes

Sponsors and contacts

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