A Clinical Trial to Evaluate the Effects of EMF Protection Devices on Sleep and Energy Levels | NCT07746011

NCT07746011

Overview

NCT ID: NCT07746011
Lead Sponsor: Life Harmony Energies, Inc.INDUSTRY
Official Title: A Clinical Trial to Evaluate the Effects of EMF Protection Devices on Sleep and Energy Levels
Brief Summary: 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.
Conditions: Sleep Disturbance

Status and Timeline

Status: Completed
Last Update Posted: Aug 4, 2026Actual
Start Date: Aug 15, 2025Actual
Primary Completion Date: Nov 15, 2025Actual
Completion Date

Participation Criteria

Ages Eligible for Study: Adult (18-64)
Sexes Eligible for Study: All
Accepts Healthy Volunteers?: No
Eligibility Criteria: 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

Study Type: Interventional
Phase: Not Applicable
Enrollment: 24Actual
Primary Purpose: Treatment
Allocation: N/A
Interventional Model: Single Group Assignment
Masking: None (Open Label)

Contacts and Locations

Central Contacts: No data available
Locations: Citruslabs

Similar Studies

NCT04737434Unknown status

The Effect of Extremely Low Frequency Electromagnetic Field Device Improving Sleep and Stress

NCT05463302Completed

Investigating the Efficacy of Sleepgift Blanket on Sleep Quality and Heart Health

NCT05001646Unknown status

Electromagnetic Field Protection Device Use Impact in Healthy Volunteers

NCT07353021Not yet recruiting

Longterm Effects of a Biofield Patch on Anxiety, Sleep, and Energy

NCT04571775Unknown status

Effects of a Lifestyle Product on Physiological Measures and Subjective Well-being in Humans: A Systematic Study

NCT03074617Completed

Electromagnetic Field Effects of Mobile Communication (LTE) on Sleep in the Context of Genetic Variation

NCT05908344Completed

Frequen-ZZZ SleepPad Investigational Device POC

NCT04301440Completed

THE PHYSIOLOGICAL EFFECTS OF ELECTROMAGNETIC EMISSIONS ON THE GENERAL CONDITION OF THE PATIENT