Neural Mechanisms of Light Driven Analgesia
A legfontosabb adatok
- Ki végzi
- University of North Carolina, Chapel Hill
- Hol
- Chapel Hill (Egyesült Államok)A helyszín megnézése
- Azonosító
- Állapot
- Toboroz
- Résztvevők
- 60 fő, tervezett
- Kezdés
- 2026. febr. 24.
- Várható befejezés
- 2030. jan. 31.
- A vizsgálat típusa
- Beavatkozással járó
- A vizsgált kezelések
- S-cone modulating visual stimulus
- Equal Energy White Visual Stimulus
- Green light visual stimulus (S-OFF)
- Evoked Pressure Pain Stimulus
- A regiszteradat frissítve
- 2026. május 13.
Ki vehet részt
MI-összefoglaló
A vizsgálat saját részvételi feltételeiből. Gép olvasta ki az oldalon álló regiszterszövegből, ezért tévedhet. Hogy ki vehet részt, azt a lenti regiszterszöveg és a vizsgálat csapata dönti el.
The trial is looking for adults with chronic muscle and joint pain (including fibromyalgia) and healthy adults. It studies how colored light changes brain activity and pain during MRI scans. 2 people with congenital stationary night blindness and no chronic pain will also join.
- Életkor
- 18 years or older
- Nem
- All sexes
- A betegség stádiuma
- People with pain must score ≥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 (2016 Fibromyalgia Questionnaire). Pain must have lasted 3 months or longer, be in 4 out of 5 body regions, and average ≥4 on a 0-10 scale over the past month.
- Korábbi kezelés
- No planned changes to medicines or treatment for the next 3 months.
A részvétel fő kizáró okai
- Eye or retina problems that harm vision, such as uveitis, cataracts or color-blindness
- Sensitivity to or dislike of light
- History of seizures
- Pregnancy
- Cannot have an MRI, for example metal implants, devices not safe for MRI, or fear of closed spaces
A regiszter feltételei, szó szerint
Mind a 18 feltétel megnézéseKevesebb
Ki vehet részt
- 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
- 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
- -2 additional participants without chronic MSP will be recruited with diagnosed congenital stationary night blindness
Ki nem vehet részt
- Plans for analgesic treatment plan changes in next 3 months (surgery, analgesic medication changes, injections, pain procedures, etc)
- 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
- 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
Helyszínek itt: Egyesült Államok
- University of North Carolina at Chapel HillChapel Hill, Egyesült ÁllamokContact: Matthew Mauck, MD, PhDRésztvevőt keres
A vizsgálatról
Mit akar kideríteni a vizsgálat
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.
A vizsgálat csoportja
- Light sequence during imagingA vizsgált kezelés
The sequence of stimulus presentation for resting state scans will be Equal Energy White (with luminance modulation) for 8 minutes then Static Green for 8 minutes, followed by an anatomical scan, then S-cone modulating stimuli for 8 minutes.
Kezelés: S-cone modulating visual stimulus, Equal Energy White Visual Stimulus, Green light visual stimulus (S-OFF) és Evoked Pressure Pain Stimulus
Kérdések a vizsgálat csapatának
- Milyen gyakran kell bejárnom, és egy-egy alkalom mennyi ideig tart?
- Megtérítik az utazási költséget?
- Megtarthatom a saját orvosomat?
- Mi történik, ha ki akarok lépni?
Contact the study team: see the registry record → Contacts and Locations
Oldal nyomtatása az orvosomnakAdatok és források
- Regiszteradat
- Szerepel a ClinicalTrials.gov-on.
- MI-összefoglaló
- A vizsgálat saját részvételi feltételeiből. Gépi kiolvasás: 2026. november 14.
- A regiszteradat frissítve
- 2026. május 13.