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NCT07509177Recruiting

An Examination of Whether Infrared Light Therapy Can Reduce Stress in People With Epilepsy

Photobiomodulation Radiant Intervention for Stress in Epilepsy

Source: ClinicalTrials.gov · Last updated 23 Apr 2026

Brief summary (registry, in English)

Do you have Epilepsy? Would you like to participate in a study using PhotoBioModulation (PBM)? PBM is being researched for potential benefits in resolving many stress-related brain disorders. It is a non-invasive technique that delivers light energy to cells and tissues that can promote brain stabilization and self-regulation, cell repair, reduce oxidative stress, and enhance cellular function. We ask you to participate for about 3-4 months and come to our facility for 30 minute sessions 3x a week for 15 weeks. You will receive extensive metabolic testing and an Õura ring for your participation.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
80 (estimated)
First submitted
25 Mar 2026
Start date
11 Aug 2025
Primary completion date
11 Aug 2026
Lead sponsor
Cynthia Kerson
Diseases
Epilepsy
NCT number
NCT07509177

What you commit to

  • Study type: Interventional
  • Planned participants: 80
  • From 11 Aug 2025 to the primary completion date, 11 Aug 2026
  • 4 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • \-

Who the study is looking for

  • • \>18 YO
    • Epilepsy - medical diagnosis with at least one seizure within the past 6 months: diagnosis to be obtained from medical records from the treating physician by signature of HIPAA-compliant medical release form
    • Agreement to maintain or reduce medication regimen (based upon prescribers' advice)
    • Available for intake, baseline, post-treatment, 6-month follow-up assessments, and 45 sessions of PBM
    • Willingness to wear an Õura ring at all times (except for charging) for the duration of the study.
    • Exclusion:
  • \< 17 YO
  • Substance use
  • Personality disorders
  • Heavy metal toxicity
  • Mold toxicity
  • Metabolic measures thresholded based on participant type
  • Increase in current medication (dosage and/or type)
  • No new medications prescribed (reduction as prescribed by prescribing physician OK)
  • Current brain bleed
  • Acute TBI within the last 12 months
  • History of neuromodulation, including ECT
  • Brain implants/pumps/shunts
  • History of brain surgery
  • Hormone replacement therapy for menopause or gender transition
  • Untreated sleep disorders

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (4)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Right Mind Wellness Center
Coordinator of this site? Confirm its status
CincinnatiUnited StatesRecruiting
Houston Neuroscience Brain Center
Coordinator of this site? Confirm its status
HoustonUnited StatesRecruiting
Brain Health Center Miami
Coordinator of this site? Confirm its status
North MiamiUnited StatesRecruiting
Holly Maggiano, MD
Coordinator of this site? Confirm its status
WarrenUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.