Denne side blev automatisk oversat, og nøjagtigheden af ​​oversættelsen er ikke garanteret. Der henvises til engelsk version for en kildetekst.

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

3. august 2026 opdateret af: Life Harmony Energies, Inc.

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.

Studieoversigt

Status

Afsluttet

Betingelser

Intervention / Behandling

Undersøgelsestype

Interventionel

Tilmelding (Faktiske)

24

Fase

  • Ikke anvendelig

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiesteder

  • Forenede Stater
    • Nevada
      • Las Vegas, Nevada, Forenede Stater, 89118
        • Citruslabs

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

  • Voksen

Tager imod sunde frivillige

Ingen

Beskrivelse

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

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Behandling
  • Tildeling: N/A
  • Interventionel model: Enkelt gruppeopgave
  • Maskning: Ingen (Åben etiket)

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: EMF Protection Devices
Enhed: 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).

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Change in objective sleep quality
Tidsramme: Baseline, Day 2, Day 4, Week 1, Week 2, Week 3, and Week 4
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

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Change in Self-Reported Sleep
Tidsramme: Baseline, Day 2, Day 4, Week 1, Week 2, Week 3, and Week 4
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
Tidsramme: Baseline, Day 2, Day 4, Week 1, Week 2, Week 3, and Week 4
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
Tidsramme: Baseline, Day 2, Day 4, Week 1, Week 2, Week 3, and Week 4
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
Tidsramme: Baseline, Day 2, Day 4, Week 1, Week 2, Week 3, and Week 4
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
Tidsramme: Baseline, Day 2, Day 4, Week 1, Week 2, Week 3, and Week 4
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

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Sponsor

Life Harmony Energies, Inc.

Samarbejdspartnere

Citruslabs

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Faktiske)

15. august 2025

Primær færdiggørelse (Faktiske)

15. november 2025

Studieafslutning (Faktiske)

15. november 2025

Datoer for studieregistrering

Først indsendt

28. juli 2026

Først indsendt, der opfyldte QC-kriterier

3. august 2026

Først opslået (Faktiske)

4. august 2026

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

4. august 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

3. august 2026

Sidst verificeret

1. august 2026

Mere information

Begreber relateret til denne undersøgelse

Yderligere relevante MeSH-vilkår

Andre undersøgelses-id-numre

  • 20760
  • legacy-20760

Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter

Studerer et amerikansk FDA-reguleret lægemiddelprodukt

Ingen

Studerer et amerikansk FDA-reguleret enhedsprodukt

Ingen

Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .

Abonner