NCT07746011

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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
24

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Aug 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

August 15, 2025

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 15, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

November 15, 2025

Completed
9 months until next milestone

First Submitted

Initial submission to the registry

July 28, 2026

Completed
7 days until next milestone

First Posted

Study publicly available on registry

August 4, 2026

Completed
Last Updated

August 4, 2026

Status Verified

August 1, 2026

Enrollment Period

3 months

First QC Date

July 28, 2026

Last Update Submit

August 3, 2026

Conditions

Outcome Measures

Primary Outcomes (1)

  • 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 Outcomes (5)

  • Change in Self-Reported Sleep

    Baseline, Day 2, Day 4, Week 1, Week 2, Week 3, and Week 4

  • Change in Self-Reported Energy Levels

    Baseline, Day 2, Day 4, Week 1, Week 2, Week 3, and Week 4

  • Change in Self-Reported Focus

    Baseline, Day 2, Day 4, Week 1, Week 2, Week 3, and Week 4

  • Change in Self-Reported Calmness

    Baseline, Day 2, Day 4, Week 1, Week 2, Week 3, and Week 4

  • Change in Self-Reported General Well-Being

    Baseline, Day 2, Day 4, Week 1, Week 2, Week 3, and Week 4

Study Arms (1)

EMF Protection Devices

EXPERIMENTAL
Device: EMF Protection

Interventions

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).

EMF Protection Devices

Eligibility Criteria

Age30 Years - 60 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • 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

You may not qualify if:

  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Citruslabs

Las Vegas, Nevada, 89118, United States

Location

MeSH Terms

Conditions

ParasomniasSleep Initiation and Maintenance DisordersFatigue

Condition Hierarchy (Ancestors)

Sleep Wake DisordersNervous System DiseasesMental DisordersSleep Disorders, IntrinsicDyssomniasSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Sponsor Type
INDUSTRY
Responsible Party
SPONSOR

Study Record Dates

First Submitted

July 28, 2026

First Posted

August 4, 2026

Study Start

August 15, 2025

Primary Completion

November 15, 2025

Study Completion

November 15, 2025

Last Updated

August 4, 2026

Record last verified: 2026-08

Locations