Neural Mechanisms of Light Driven Analgesia
University of North Carolina, Chapel Hill · with National Institute of Neurological Disorders and Stroke (NINDS) · NCT07245303
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18+ · All sexes
- Healthy volunteers
- Accepted
- Study type
- Interventional · Not applicable
- Target enrollment
- 60
- US sites recruiting
- 1
- Study start
- February 24, 2026
- Record last updated
- May 13, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
The goal of this study will be to understand the biological mechanisms that are responsible to light-driven analgesia. Light presented to the retina has been shown to have pain relieving properties in pre-clinical and clinical studies. In this study the investigators will evaluate the functional connectivity between subcortical visual areas and non-image forming brain areas that are involved in pain sensation. The investigators will also evaluate how three colored light stimuli presented to the retina results in changes in whole brain evoked activation patterns in participants with chronic musculoskeletal pain and in healthy controls. The investigators will also assess while brain evoked activation patterns in response to a pressure pain stimulus in the presence of three light stimuli in individuals with chronic musculoskeletal pain and healthy controls.
Being studied: S-cone modulating visual stimulus; Equal Energy White Visual Stimulus; Green light visual stimulus (S-OFF); Evoked Pressure Pain Stimulus
Conditions: Musculoskeletal Pain; Fibromyalgia; Healthy Controls Group - Age and Sex-matched
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria for participants with cMSP and healthy controls (n=30)
- Adults ≥18 years of age.
- Individuals who do not have any plans for medication or treatment changes for the next 3 months.
- Participants must be willing and able to undergo an MRI.
- Participants must not be claustrophobic
- Participants must be alert and oriented and able to provide informed consent.
- Individuals must be able to speak and read English.
Inclusion Criteria for participants with cMSP only (n=30)
- To be eligible, participants must have a score of ≥7 on the Widespread pain index (WPI) and ≥5 on the symptom severity scale (SSS), or 4-6 on the WPI and ≥9 on the SSS in the 2016 Fibromyalgia Questionnaire.
- Pain symptoms must have been present for 3 months or longer.
- Pain must be present in 4 out of 5 body regions.
- Individuals enrolled will have an average pain severity ≥4 on the 0-10 NRS over the month prior to enrollment to recruit individuals with moderate to severe chronic MSP.
Inclusion Criteria for Participants with Congenital Stationary Night Blindness (n=2)
-2 additional participants without chronic MSP will be recruited with diagnosed congenital stationary night blindness
Exclusion Criteria
- Presence of retinal vision disorders or conditions resulting in vision impairment.
- Patient-reported photosensitivity, photophobia, or aversion (as may occur in autoimmune diseases such as systematic lupus erythematosus).
- Disorders including uveitis, cataracts, color-blindness, history of seizure disorder.
- Plans for analgesic treatment plan changes in next 3 months (surgery, analgesic medication changes, injections, pain procedures, etc).
- Prisoner Status.
- Pregnancy.
- Contraindications to MRI imaging. These include the presence of implanted/embedded ferromagnetic materials, implanted medical devices that are not MRI compatible, and claustrophobia.
Recruiting US locations
University of North Carolina at Chapel Hill
Chapel Hill, NC 27599
Site contact: Matthew Mauck, MD, PhD · 919-966-5136 · matt_mauck@med.unc.edu
Study contacts (from the official record)
- Matthew Mauck, MD, PhD · 919-966-5136 · matt_mauck@med.unc.edu
Similar studies in North Carolina
All pain studies in North Carolina →- RecruitingHealthy volunteersOvernight stay mentioned
The Osteoarthritis Prevention Study
Wake Forest University
- Location
- Winston-Salem, NC + 1 other US site
- Eligibility basics
- Ages 50+ · Women only
- RecruitingPhase 3
Efficacy and Safety of VER-01 in the Treatment of Participants With Chronic Painful Lumbosacral Radiculopathy
Vertanical GmbH
- Location
- Monroe, NC + 22 other US sites
- Eligibility basics
- Ages 18+
- RecruitingPhase 1
Study to Evaluate Safety of C-1101 Versus Sterile Saline in Adults With Chronic Painful Lumbosacral Radiculopathy
Consano Bio
- Location
- Winston-Salem, NC + 1 other US site
- Eligibility basics
- Ages 18–70
- Recruiting
MagnetOs Flex Matrix Compared to Trinity Elite Mixed With Local Autograft in Patients Undergoing up to Four-level Instrumented Posterolateral Fusion
Kuros Biosurgery AG
- Location
- Pinehurst, NC + 8 other US sites
- Eligibility basics
- Ages 18+