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Electromagnetic Field Protection Device Use Impact in Healthy Volunteers

Clinical and Molecular Impact of In-home Resonance-based Electromagnetic Field Protection Device Usage in Healthy Individuals

Status
UNKNOWN
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05001646
Enrollment
44
Registered
2021-08-12
Start date
2022-03-31
Completion date
2023-04-30
Last updated
2022-03-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Aging, Aging Well

Brief summary

This is a prospective, single group, self-controlled study to evaluate the clinical and molecular impact of continuous in-home resonance-based electromagnetic field (EMF) protection device usage in healthy individuals.

Interventions

DEVICEIn-home resonance-based electromagnetic field protection device

Participants will have an in-home EMF protection device

Sponsors

Blushield USA
CollaboratorUNKNOWN
TruDiagnostic
Lead SponsorINDUSTRY

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
30 Years to 70 Years
Healthy volunteers
Yes

Inclusion criteria

* Any sex, gender orientation, and ethnicity * Between ages 30 and 70 * Must be willing and able to participate in venipuncture, health history and clinical assessments, passive monitoring (Oura ring), and continuous in-home Blushield device usage

Exclusion criteria

* Significant change in diagnosis and/or treatment of major illness or injury within 2 years prior to screening, e.g., diabetes, cancer, cardiovascular disease, psychiatric condition 2. Any ongoing immune system concerns or immunodeficiency disease * History of any viral illness in preceding year * Body mass index (BMI) \> 35 kg/m2 * Presence of active infection * Any other illness, disorder, alcohol or chemical dependence that in the opinion of investigators would render study participation unsuitable * Unable or unwilling to provide required biological sample * Unable or unwilling to avoid pregnancy during study period

Design outcomes

Primary

MeasureTime frame
Epigenetic TestingChange from baseline to 12 weeks

Contacts

Primary ContactNatalie Amalani
natalie@blushield-us.com816-377-4651
Backup ContactAnnie Prestrud
annie@trudiagnostic.com

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026