2021 PMT iAge® Intervention Trial by Edifice Health

Edifice Health

Status: Terminated

Conditions: Inflammaging; Chronic Inflammation

Treatments: Other: Placebo; Dietary Supplement: Dietary supplement

Study type: Interventional

Funder types: Industry

Identifiers

NCT04983017

EH_21_01_PMT_iAge_INT

Details and patient eligibility

About

This is a decentralized, double-blind, randomized, placebo-controlled study to assess the effectiveness of different dietary supplements in decreasing systemic chronic inflammation (SCI) and lowering inflammatory age (iAge®). iAge® is a metric for age-related chronic inflammation and immune function decline calculated from a standard blood draw utilizing immune phenotyping and artificial intelligence algorithms. SCI is a natural process that occurs within the body. It is believed to accelerate the process of biological aging. As opposed to acute inflammation, iAge® is not a reflection of illness, infection, trauma or injury. It naturally occurs in the ambulatory healthy population as we age as a function of the body.

This study will use immunotype specific dietary supplement formulations to improve a participant's Inflammatory Age® (iAge®).

Full description

This decentralized, double-blind, randomized, placebo-controlled study will identify interventions that may lower a participant's inflammatory age (iAge®) and will increase the number of participants with objective and subjective health information that have associated iAge® scores. The study will also (1) correlate secondary endpoints with baseline and subsequent iAge® scores, (2) confirm the compatibility of the iAge® test with the Tasso device, ADX100 or ViveBio home blood collection systems, and (3) confirm the compatibility of the iAge® test with saliva home sample collection kit.

Ambulatory adults, 18 years old and over of diverse ethnicities will be invited to participate in this study from a single site in Marin County. We will choose an equal number of male and female participants by selecting households within a 60 mile radius of the study site.

The study involves fasting blood sample collection to measure and characterize immunomes and inflammatory biomarkers, metabolites, lipid panel, hemoglobin, hemoglobin A1C, and high-sensitivity c-reactive protein (hsCRP). Participants will be asked to provide a blood sample by routine venipuncture at Baseline and approximately 2, 4 and 7 months after the start of the dietary supplement/placebo.

Participants will be given interventions to be taken daily based on their associated immunogroup cluster after each iAge® test is completed. Participants can continue on their current supplements but should not start any new supplements except those given by the study. This study has a different intervention for nine of the ten immunotype clusters. All interventions are i) generally recognized as safe (GRAS) or ii) from compounds at similar concentrations to those found in foods. Participants will be placed in one of ten immunotype clusters after each iAge® test and randomized either to a placebo or the given formulation to be taken once daily (either one, two or three pills depending on the formulation). A participant who changes his/her immunotype cluster after a follow up iAge® test will be given a new dietary intervention (or placebo based on their previous category).

All participants will also be given a Whoop wearable watch to collect information on strain, sleep and heart rate variability. Participants will be asked to complete questionnaires assessing mood, stress level, well-being, cognition, health and lifestyle. We will also obtain the following measurements: (1) Height and weight, (2) blood pressure, (3) waist and hip measurements, (4) pulse wave velocity (PWV) to measure arterial stiffness (5) timed up and go to assess frailty and (6) facial and scalp photos.

A gut microbiome sampling using a third party kit for fecal collection will be obtained at each designated time point from those participants who agree to have fecal sample collection. A subset of participants will have the following procedures done at any time point during the study: (1) saliva collection, (2) heel bone density, (3) audiometry test, (4) home blood sample collection using the Tasso device, ADX100, and ViveBio device.

Enrollment: 781 patients

Sex: All

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• 18+ years old
• Ambulatory
• Willing and able to comply with the study protocol

Exclusion criteria

• Participants with any condition that may preclude venipuncture or venous blood draws will be excluded.
• Participants with known allergies to interventions will be removed from the study.
• Vulnerable subjects including children, employees and those with cognitive disabilities will not be included in this study.
• Male participants on iron supplementation
• Participants on >1 mg manganese, >5 mg biotin
• Pregnant women
• Nursing women
• Membership in the clinical study team
• Any condition that might interfere with volunteer safety, study objectives or the ability of the participant to understand or comply with the study protocol

At the time of enrollment:

• Active systemic or serious concurrent illness
• History of immunodeficiency
• Any known or suspected impairment of immunologic function
• Diabetes mellitus treated with any diabetic medication
• Moderate to severe renal disease
• Blood pressure greater than 140/90
• Chronic hepatitis B or C
• Recent or current use of immunosuppressive medication
• Malignancy other than squamous cell or basal cell skin cancer, including solid tumors such as breast cancer or prostate cancer with recurrence in the past year, and any hematologic cancer such as leukemia, which might jeopardize volunteer safety or compliance with the protocol
• Autoimmune disease
• Auto-inflammatory disease
• History of blood dycrasias or hemoglobinopathies requiring regular medical follow up or hospitalization during the preceding year
• Use of any anticoagulation medication
• A medical or psychiatric condition or occupational responsibilities that would preclude subject compliance with the protocol
• History of Guillain-Barre syndrome

Trial design

Primary purpose: Other

Allocation: Randomized

Interventional model: Factorial Assignment

Masking: Double Blind

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781 participants in 2 patient groups, including a placebo group

Dietary supplements

Active Comparator group

Description:

Dietary supplements are either (1) designated as Generally Recognized As Safe (GRAS) by the Food and Drug Administration or (2) compounds at similar concentrations to those found in foods.

Treatment:

Dietary Supplement: Dietary supplement

Placebo

Placebo Comparator group

Description:

Placebo-matched formulations

Treatment:

Other: Placebo