A Study to Evaluate the Effects of a Beef Liver Supplement on Energy, Mood, and Mental Clarity
2 other identifiers
interventional
100
1 country
1
Brief Summary
This is a randomized, triple-blind, placebo-controlled clinical trial evaluating the effects of the Ancestral Supplements Grass Fed Beef Liver oral supplement on energy, mood, and mental clarity over 12 weeks. One hundred male and female participants aged 18-50 who report concerns regarding energy levels, mood, and mental clarity will be enrolled and randomized equally into an intervention arm (beef liver supplement) or a placebo arm. Participants will take their assigned product once daily and complete self-reported questionnaires at Baseline, Week 4, Week 8, and Week 12. Blood testing (iron panel) will be conducted at Baseline and Week 12 at a local Quest Diagnostics Clinic. The primary objective is to evaluate the product's effects on energy and mood; the secondary objective is to assess participants' perceptions of the product's effects on energy, mood, and mental clarity, including happiness, anxiety, well-being, brain fog, and concentration.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Sep 2026
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
September 1, 2026
CompletedFirst Submitted
Initial submission to the registry
October 19, 2026
CompletedFirst Posted
Study publicly available on registry
October 23, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 1, 2026
October 23, 2026
October 1, 2026
3 months
October 19, 2026
October 19, 2026
Conditions
Outcome Measures
Primary Outcomes (3)
Change in Iron Status
Change in blood iron levels assessed via iron panel blood test (Quest Diagnostics, iron test code 001339)
Baseline and Week 12
Change in Energy Levels
Change in self-reported energy levels assessed via self-reported questionnaire
Baseline, Week 4, Week 8, and Week 12
Change in Mood
Change in self-reported mood assessed via self-reported questionnaire
Baseline, Week 4, Week 8, and Week 12
Secondary Outcomes (6)
Change in Self-Reported Vitality
Baseline, Week 4, Week 8, and Week 12
Change in Self-Reported Happiness
Baseline, Week 4, Week 8, and Week 12
Change in Self-Reported Anxiety
Baseline, Week 4, Week 8, and Week 12
Change in Self-Reported Well-being
Baseline, Week 4, Week 8, and Week 12
Change in Self-Reported Brain Fog
Baseline, Week 4, Week 8, and Week 12
- +1 more secondary outcomes
Study Arms (2)
Intervention (Beef Liver Supplement)
EXPERIMENTALPlacebo Comparator
PLACEBO COMPARATORInterventions
Participants receive the Ancestral Supplements Grass Fed Beef Liver supplement (Grass Fed Liver \[Bovine\], 3000 mg per serving of 6 capsules) taken once daily, with a graduated dose escalation from 1 capsule/day over the first 18 days up to the full serving of 6 capsules/day, for 12 weeks.
Participants receive a matched placebo product (microcrystalline cellulose and natural food color) taken once daily using the same dosing regimen as the intervention arm, for 12 weeks. The taste and appearance of the placebo are matched to the test product.
Eligibility Criteria
You may qualify if:
- Be male or female
- Be aged 18-50
- Anyone experiencing issues regarding all of the following over the past four weeks: energy levels, mood, and mental clarity
- Anyone who is generally healthy - does not live with any uncontrolled chronic disease
- Anyone who is willing to maintain their current diet, sleep schedule, and activity level for the duration of the study
- Resides in the United States
You may not qualify if:
- Anyone with pre-existing chronic conditions that would prevent participants from adhering to the protocol, including oncological and psychiatric disorders
- Currently taking iron supplements or being treated for anemia
- Anyone currently taking oral contraceptives that contain iron
- Anyone currently taking vitamin A supplements, or supplements that contain vitamin A
- Anyone with any allergies or sensitivities to any of the study product ingredients
- Any women who are pregnant, breastfeeding, or trying to conceive (or who will be at any point during the study period)
- Anyone with hemochromatosis
- Anyone unwilling to follow the study protocol
- Has stopped using hormonal birth control in the past month
- Anyone who is vegan and/or does not consume animal products for any reason
- Anyone who is considered to be a heavy drinker (i.e. 8 or more alcoholic drinks per week for women or 15 or more alcoholic drinks per week for men)
- Planning on introducing any products or any new forms of prescription medication or supplements that target energy levels, mood, or mental clarity, during the study duration
- Currently partaking in another research study or will be partaking in any other research study at any point during this study's duration
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Ancestral Supplements, LLClead
- Citruslabscollaborator
Study Sites (1)
Citruslabs
Las Vegas, Nevada, 89118, United States
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- TRIPLE
- Who Masked
- PARTICIPANT, INVESTIGATOR, OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- INDUSTRY
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
October 19, 2026
First Posted
October 23, 2026
Study Start
September 1, 2026
Primary Completion (Estimated)
December 1, 2026
Study Completion (Estimated)
December 1, 2026
Last Updated
October 23, 2026
Record last verified: 2026-10