A Clinical Trial to Evaluate the Effects of EMF Protection Devices on Sleep and Energy Levels

This study evaluates the effects of a selection of EMF protection devices (Home Harmonizers, Better ZZZs, iCell Chip, Car Harmonizer, Laptop Chip, XL Band, and Device Chips) on sleep quality, sleep quantity, and energy levels in adults aged 30-60 who currently experience sleep difficulties. The trial is a single-arm, unblinded, virtual study conducted over 4 weeks and 4 days (including a 4-day calibration period).

Twenty-four participants will use all test products daily and complete self-reported questionnaires at Baseline, Day 2, Day 4, Week 1, Week 2, Week 3, and Week 4. Objective sleep data will be collected via an Oura Generation 3 ring worn throughout the study. Secondary outcomes include participants' perceptions of effects on sleep, energy, focus, and general well-being.

Study Overview

• Status: Completed
• Conditions: Fatigue; Insomnia; Sleep Disturbance; Electromagnetic Field Exposure
• Intervention / Treatment: Device: EMF Protection

• Study Type: Interventional
• Enrollment (Actual): 24
• Phase: Not Applicable

Contacts and Locations

Study Locations

• United States
  • Nevada
    • Las Vegas, Nevada, United States, 89118
      • Citruslabs

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: Adult
• Accepts Healthy Volunteers: No

Description

Inclusion Criteria:

• Be male or female
• Be aged 30-60
• Anyone currently experiencing issues regarding any of the following: sleeping, falling asleep, staying asleep, or failing to feel refreshed after sleep
• Must have all of the following items: bed with a foam or spring mattress, a car with a single cigarette lighter, iPhone 12, 13, 14, 15, or 16, laptop, and Wi-Fi router
• Must have at least two of the following: Wi-Fi extender, smart TV, personal computer, ceiling fan in the bedroom, air purifier
• Must have access to where the electricity enters the home, such as an electric (smart) meter outside, the pipe closest to the electric meter, or the fuse box inside the home
• If taking any products, medications, or supplements that target sleep and/or energy during the test period, has been doing so consistently for three months, and is willing to maintain this routine for the duration of the study
• Willing to maintain their current diet, sleep schedule, and activity level for the duration of the study
• Must be able to sleep at home consistently and must not plan to travel for business, vacation, or any other reason during the study period
• Anyone who lives in a single-family residence (i.e., no apartments, condos, or mobile homes)
• Willing to stop using a cellphone watch for the duration of the study
• Must be willing to wear a wristband all day, shaped much like a cellphone watch, and to remove it at night while sleeping
• Willing to remove any other fitness tracking or sleep tracking devices during the study, such as Fitbits, Garmin, and Whoop products
• Must be willing to wear an Oura Ring 24 hours per day during the duration of the study
• Resides in the United States

Exclusion Criteria:

• Anyone with pre-existing chronic conditions that would prevent participants from adhering to the protocol, such as cancer, auto-immune conditions, mental health disorders, history of serious illness in the last three months, history of substance abuse, or planned surgery during the study period
• Sleeps on any of the following beds: adjustable beds, beds equipped with grounding mats, or any bed that connects to an electrical outlet
• Anyone with a sleep-related condition or disorder
• Anyone who is pregnant, breastfeeding, or trying to conceive (or who will be at any point during the study period)
• Anyone who drinks heavily (i.e., 8 or more alcoholic drinks per week for women or 15 or more alcoholic drinks per week for men)
• Anyone who lives within 50 miles of a military base or one block of XL powerlines or a cell tower
• Anyone who lives in a rural/country home
• Anyone unwilling to follow the study protocol
• Currently partaking in another research study and will not be partaking in any other research study for the next four weeks or at any point during this study's duration
• Anyone who has Starlink internet or fiber-optic internet

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: N/A
• Interventional Model: Single Group Assignment
• Masking: None (Open Label)

Number of Arms

1

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: EMF Protection Devices	Device: EMF Protection; All participants receive and use all test products simultaneously: 2 Home Harmonizers, 1 Better ZZZs pad (placed under mattress), 1 iCell Chip (for iPhone 12-16), 1 Car Harmonizer (inserted into car cigarette lighter), 1 Laptop Chip, 1 XL Band (worn on wrist during waking hours), and 8 Device Chips (placed on household EMF-emitting devices).

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Change in objective sleep quality	Assessed using Oura Generation 3 ring sleep metrics. Change from baseline will be evaluated at each subsequent assessment.	Baseline, Day 2, Day 4, Week 1, Week 2, Week 3, and Week 4

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Change in Self-Reported Sleep	Assessed using validated sleep questionnaire total score(s). Change from baseline will be evaluated at each subsequent assessment.	Baseline, Day 2, Day 4, Week 1, Week 2, Week 3, and Week 4
Change in Self-Reported Energy Levels	Assessed via self-reported questionnaire measuring participants' perceptions of the product's effects on energy levels	Baseline, Day 2, Day 4, Week 1, Week 2, Week 3, and Week 4
Change in Self-Reported Focus	Assessed via self-reported questionnaire measuring participants' perceptions of the product's effects on focus	Baseline, Day 2, Day 4, Week 1, Week 2, Week 3, and Week 4
Change in Self-Reported Calmness	Assessed via self-reported questionnaire measuring participants' perceptions of the product's effects on calmness	Baseline, Day 2, Day 4, Week 1, Week 2, Week 3, and Week 4
Change in Self-Reported General Well-Being	Assessed via self-reported questionnaire measuring participants' perceptions of the product's effects on general well-being	Baseline, Day 2, Day 4, Week 1, Week 2, Week 3, and Week 4

Collaborators and Investigators

• Sponsor: Life Harmony Energies, Inc.
• Collaborators: Citruslabs

Study record dates

Study Major Dates

• Study Start (Actual): August 15, 2025
• Primary Completion (Actual): November 15, 2025
• Study Completion (Actual): November 15, 2025

Study Registration Dates

• First Submitted: July 28, 2026
• First Submitted That Met QC Criteria: August 3, 2026
• First Posted (Actual): August 4, 2026

Study Record Updates

• Last Update Posted (Actual): August 4, 2026
• Last Update Submitted That Met QC Criteria: August 3, 2026
• Last Verified: August 1, 2026

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Nervous System Diseases; Mental Disorders; Sleep Wake Disorders; Sleep Disorders, Intrinsic; Dyssomnias; Pathological Conditions, Signs and Symptoms; Signs and Symptoms; Parasomnias; Fatigue; Sleep Initiation and Maintenance Disorders
• Other Study ID Numbers: 20760; legacy-20760

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No