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A Study to Observe Well-Being in Healthy Volunteers Using Healy Zero Hertz

An Observational, Prospective, Open-Label Pilot Study to Evaluate Psychophysiological Wellbeing with Use of Healy Zero Hertz on Healthy Volunteers - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2026/03/105158
Enrollment
50
Registered
2026-03-02
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-30

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

Conditions

None listed

Interventions

Intervention1: Nil: Nil Intervention2: Nil: Nil

Sponsors

Gaya International & Co.
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1 Male and female participants aged 18 years and above 2 Willing to provide written informed consent prior to any study-specific procedures being performed 3 The study will be done on healthy volunteers identified by the investigators of the study 4 Participant is able to comply with study procedures and protocol requirements throughout the study period

Exclusion criteria

Exclusion criteria: 1 Any finding in the medical examination including BP PR Body Temp etc is clinically significant as per the investigator 2 Persons having any device like a pacemaker implant with an electrical interface batteries or cochlear implants 3 Pregnant and lactating women 4 Anyone using a mobile phone Laptop for less than 2 hours 5 Participation in another clinical study within 30 days prior to screening of the current study 6 Evidence of immediate life threatening disease or a life expectancy of less than 3 months as per the Investigator s clinical judgement 7 Any history of a medical or psychiatric condition that in the opinion of the investigator(s) could affect the participant safety or interfere with the study assessments 8 Participants with any clinically significant acute or chronic medical condition that in the opinion of the Investigator may interfere with study participation or the assessment of outcomes

Design outcomes

Primary

MeasureTime frame
Change in Overall Wellness, comfort and digital fatigue from baseline to end-of-study (Day 14, +2) assessed using Healy Wellness and Psychophysiological Response Scale (HWPRS)Timepoint: Day 14

Secondary

MeasureTime frame
1. Change from baseline to Day 14 (+2 days) in participant reported relaxation, focus, & calmness scores associated with use of the Healy Zero Hertz Cap. 2. Change from baseline to Day 14 (+2 days) in sleeping pattern, sleep efficiency, & post-sleep wellness reported with use of the Healy Zero Hertz Mask. 3. Change from baseline to Day 14 (+2 days) in overall fabric comfort & mental refreshment scores related to use of the Healy Zero Hertz BlanketTimepoint: The outcomes will be assessed at baseline (Day 0) & at the end-of-study visit on Day 14 ( 2 days), as per the study protocol & schedule of assessments.

Countries

India

Contacts

Public ContactGaurav Rao

Yadav Hospital

drgauravrao@yahoo.co.in7290005252

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Apr 4, 2026