Heart & Soil Lifeblood for iron levels and energy
Evaluating Heart & Soil's Lifeblood on Iron and Energy Levels
This remote program will see if taking Heart & Soil Lifeblood raises iron levels and helps adults feel more energetic.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 100 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Efforia, Inc Industry-sponsored |
| Locations | 1 site (New York, New York) |
| Trial ID | NCT07293117 on ClinicalTrials.gov |
What this trial studies
This decentralized, remotely administered trial asks participants to take the Heart & Soil Lifeblood supplement and completes iron testing before and after the supplementation period. Investigators will collect a comprehensive iron panel and correlate lab changes with participant-reported energy and fatigue via surveys. The design focuses on a natural, freeze-dried organ extract product rather than standard synthetic iron sulfate supplements. Participants are screened for safety exclusions such as hemochromatosis, pregnancy, GI disorders, certain medications, and severe allergies.
Who should consider this trial
Good fit: US adults who report low energy, can read English, are willing to participate remotely, and who are not pregnant/nursing, not diagnosed with hemochromatosis, not on iron-related medications, and without excluded GI or severe allergy conditions.
Not a fit: People with hemochromatosis, those taking iron therapies, pregnant or nursing people, and those with the listed exclusionary GI or severe allergy conditions are unlikely to benefit and are excluded for safety.
Why it matters
Potential benefit: If effective, Lifeblood could provide a natural supplement option to increase iron stores and reduce fatigue for some people.
How similar studies have performed: While synthetic iron supplements have well-established clinical evidence, controlled clinical data on freeze-dried organ extract products like Lifeblood are limited and this approach is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Can read and understand English. * US resident. * Willing and able to follow the requirements of the protocol. Exclusion Criteria: * Individuals with Hemochromatosis * Individuals with Severe Allergies * Pregnant or Nursing Women * Individuals with Gastrointestinal Disorders * Individuals on Iron-Related Medications * Individuals with Mental Health Disorders * Competitive Athletes
Where this trial is running
New York, New York
- Efforia — New York, New York, United States (Recruiting)
Study contacts
- Study coordinator: Matthew Amsden
- Email: help@efforia.com
- Phone: 646-679-2479
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.