Light-based immune boost to help prevent viral upper respiratory infections
Official title: Light-based Immunomodulation for Guarding Against Human Respiratory Tract Infections
Run by Mike O'Callaghan Military Hospital · NCT07610967 · Data updated 2026-11-12
A daily handheld light therapy device is tested to see if it can lower how often adults at a military medical facility get colds, flu, or other upper respiratory infections.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 130 (estimated) |
| Sponsor | Mike O'Callaghan Military Hospital Federal |
| Locations | 1 site (Nellis Air Force Base, Nevada) |
| Status | Recruiting |
| Started | October 1, 2026 |
| Main results expected | June 2028 |
| Study ends | June 2028 |
| Registry record updated | October 26, 2026 |
| Trial ID | NCT07610967 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Active duty personnel or DoD beneficiaries aged 18+ employed at Mike O’Callaghan Military Medical Center (Nellis AFB, NV).
✕Probably not a fit
Individuals with very low risk of URI or those unable to use the device as instructed may not experience benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This randomized trial compares an active photobiomodulation device (RD-X19) with a sham device in adults 18+ working at a DoD and VA medical facility. Participants use the device at home every other day for five minutes, starting from enrollment, with baseline and symptom-driven viral PCR testing to identify infections. Research staff monitor symptoms biweekly and perform daily check-ins during active illness to track outcomes such as symptom duration, work days missed, healthcare visits, and medication use. Eligibility focuses on active duty or DoD beneficiaries at the Mike O’Callaghan Military Medical Center, with exclusions for procedures that would interfere with device use. The study aims to determine whether this home-use device can reduce incidence and impact of respiratory viral infections.
Why it matters
Potential benefit: If successful, participants may experience fewer infections or milder symptoms, with fewer work absences and healthcare visits.
How similar studies have gone: Previous safety work supports the device; this trial tests effectiveness in preventing infections.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Active Duty and DoD Beneficiaries (i.e. former military, spouse, dependent child) aged 18 years and older who work in the Mike O'Callaghan Military Medical Center at Nellis Air Force Base. Exclusion Criteria: * Unable to comfortably insert RD-X19 into the mouth and keep in place for 5 minutes * Plans for head, neck or mouth surgery during the study period * Plans for major dental procedures (ie implants, wisdom teeth extraction etc) during the study
Where it's running
-
Mike O'Callaghan Military Medical Center
Nellis Air Force Base, Nevada, United States Recruiting
Study contacts
- Study coordinator: Sandra Huffman
- Email: Sandra.g.huffman.ctr@health.mil
- Phone: 7026533583
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.