Try EmeraldLED green light to support better body composition
Discover Better Body Composition With Green Light!
This remote program will test whether twice‑weekly 15‑minute EmeraldLED green light sessions help adults in the US improve body composition and overall well‑being.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 100 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Efforia, Inc Industry-sponsored |
| Locations | 1 site (New York, New York) |
| Trial ID | NCT07282080 on ClinicalTrials.gov |
What this trial studies
This decentralized, remotely administered program uses EmeraldLED green light sessions delivered for 15 minutes twice a week to explore effects on body composition and subjective well‑being. Participants will be recruited through a network of wellness locations and complete remote data collection, including body composition measures and self‑reported well‑being feedback. The sponsor will provide personalized feedback to participants about their changes over the participation period. Individuals with eye conditions are excluded and participants must be US residents who can read and follow the protocol.
Who should consider this trial
Good fit: Adults in the United States without eye conditions who can read English and are willing to follow a twice‑weekly, 15‑minute EmeraldLED green light regimen and provide body composition and well‑being data.
Not a fit: People with existing eye conditions, those unable to comply with the protocol, or those seeking rapid or large weight loss are unlikely to benefit from this intervention.
Why it matters
Potential benefit: If effective, this approach could offer a noninvasive, low‑time‑commitment option to support modest improvements in body composition and well‑being.
How similar studies have performed: Related photobiomodulation work with red or near‑infrared light has produced mixed and limited results, and green‑light effects on body composition remain largely untested beyond anecdotal reports.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Can read and understand English. * US resident. * Willing and able to follow the requirements of the protocol. Exclusion Criteria: -individuals with eye conditions
Where this trial is running
New York, New York
- Efforia — New York, New York, United States (Recruiting)
Study contacts
- Study coordinator: Matthew Amsden
- Email: help@efforia.com
- Phone: 646-679-2479
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.