Evaluating Heart & Soil's Lifeblood on Iron and Energy Levels

Efforia, Inc

Status: Enrolling

Conditions: Energy

Treatments: Dietary Supplement: Heart & Soil Lifeblood

Study type: Interventional

Funder types: Industry

Identifiers

NCT07293117

40434

Details and patient eligibility

About

This study explores how Heart & Soil's Lifeblood impacts iron levels and energy.

Full description

This remotely administered decentralized trial is designed to meticulously investigate the testimonials provided by individuals who have experienced changes in their iron levels and energy after using Heart & Soil's Lifeblood supplement. Recognizing the pivotal role of iron in red blood cell formation, oxygen transport, and numerous other physiological processes, this study aims to bridge the gap in current research concerning the effects of natural products, particularly freeze-dried organ extracts, on human biology. Unlike the extensively studied synthetic iron sulfate supplements, the study focuses on exploring the benefits of a natural alternative, aiming to enhance the understanding of how such products can support healthy iron stores and, by extension, improve overall vitality.

The objective of this study is to empower participants with personalized data and insights regarding their iron and energy levels. Through the evaluation of a comprehensive iron panel conducted before and after the supplementation of Lifeblood, investigators intend to establish a correlation between these iron levels and the perceptions of energy and fatigue, as reported through supplementary survey data. This approach transcends the realm of generic claims, delving into tangible, real-world outcomes that are directly influenced by participant engagement.

The specific aim is to quantify the impact of Lifeblood supplementation on iron levels and the subsequent enhancement of energy levels, thereby providing participants with personalized health insights. This will not only offer tailored feedback on how the supplement influences individual vitality but will also empower participants with the knowledge to make informed lifestyle decisions based on their unique health profiles.

The significance of this study lies in its potential to revolutionize the way individuals perceive and manage their energy levels through the consumption of natural, whole food, organ extracts. By integrating clinical studies with scientific rigor, investigators are set to validate the real-world experiences of individuals using supplementation to support their health. Although individual results may vary, the anticipated outcome is a personalized understanding of the role of iron in energy maintenance, presenting participants with a navigational tool for future wellness decisions. This study represents a pivotal step towards elevating our understanding of natural health products and their potential to enrich human health and vitality.

Enrollment: 100 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

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

Trial design

Primary purpose: Health Services Research

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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100 participants in 1 patient group

Single arm where participants act as their own control

Experimental group

Description:

Single Arm observational where participants act as their own control

Treatment:

Dietary Supplement: Heart & Soil Lifeblood