Red light therapy
and migraines
Ten million people in the UK live with migraines. Most manage it with triptans, Botox, or ibuprofen and hope for the best. The evidence on light therapy is more interesting than most people know about.
A condition that medicine still doesn't fully understand
If you have migraines, you already know that "it's just a headache" doesn't begin to cover it. The nausea, the light sensitivity, the hours or days of being completely non-functional - it's a neurological event, not a head complaint. And despite decades of research, the options remain limited. Triptans work for some people and not others. Preventive beta-blockers or topiramate come with side effects that can feel almost as disabling as the migraines themselves. Botox injections, every three months, for the rest of your life. CGRP inhibitors are the newest addition and genuinely effective, but expensive and not available to everyone on the NHS.
A lot of people with migraines spend years cycling through treatments, looking for something that works consistently without making their daily life harder. That's the context in which light therapy research is worth paying attention to - not as a miracle alternative, but as a genuine non-pharmaceutical option with a clinical evidence base that is more developed than most people realise.
One thing worth knowing upfront: the green light story is separate from the red light story, the mechanism is completely different, and the results in some studies are striking in their own right.
The scale of it
Migraine is the second leading cause of disability globally according to the World Health Organisation. More than a billion people worldwide are affected, a figure that has grown by over 58% in the past 30 years. In the UK, the Migraine Trust puts the number at approximately ten million people, with more than a million of those living with chronic migraine - defined as 15 or more headache days per month. Women are three times more likely to be affected than men, and the condition is most prevalent in people aged 20-40, which means a significant proportion of sufferers are managing it through their working years.
Only about half of people with migraine have seen a healthcare provider for it in the last 12 months, according to WHO data. The reasons are familiar: misdiagnosis, being told to just manage it with over-the-counter medication, or being in a cycle where preventive treatments either don't work well enough or cause side effects that make them impractical. It's a condition that is simultaneously extremely common and extremely poorly served.
What actually happens during a migraine
The full biology of migraines is still being worked out - which is part of why treating them is so difficult. What we do know is that a migraine involves a cascade of neurological events, not just blood vessel dilation. The current understanding centres on a few key processes that are relevant to why light therapy has any plausible effect at all.
The biology behind why light therapy is relevant
The trigeminal nerve releases inflammatory neuropeptides including CGRP, which dilates blood vessels and sensitises pain receptors in the meninges. PBM at red and NIR wavelengths has been shown to modulate inflammatory neuropeptide release and reduce peripheral sensitisation in pain pathways.
Elevated prostaglandins, cytokines, and oxidative stress in brain tissue drive the sustained pain phase. PBM's anti-inflammatory effects via NF-kB suppression and reduction of pro-inflammatory cytokines are well-established - the same pathway relevant to chronic pain more broadly.
Low serotonin is associated with migraine attacks - it causes blood vessel dilation and lowers pain threshold. PBM has been shown to increase serotonin levels in clinical studies. Nitric oxide modulation, another established PBM effect, influences vascular tone directly relevant to migraine pathophysiology.
None of this means red light therapy is targeting migraines the way a CGRP inhibitor does - that would be an overstatement. What it means is that the mechanisms PBM is known to affect are directly relevant to migraine pathophysiology. The question is whether that translates into clinical benefit, and that's what the trials were designed to answer.
A migraine attack - four phases and where PBM acts
Hours to days before
Mood changes, fatigue, food cravings, neck stiffness. Neurological changes are already underway before any head pain begins.
PBM potential
Regular preventive use targets the inflammatory and vascular environment before the cascade begins.
20-60 minutes
Visual disturbances, tingling, speech changes. Caused by cortical spreading depression - a wave of electrical activity across the brain.
PBM potential
Not all migraines involve aura. PBM's role here is less studied than in the headache phase.
4-72 hours
Throbbing head pain, nausea, light and sound sensitivity. Trigeminovascular activation and neuroinflammation are at their peak.
PBM potential
The Loeb RCT demonstrated reductions in pain intensity and headache days. Green light shows benefit in reducing pain during this phase.
Hours to days after
Exhaustion, brain fog, sensitivity. Often called the "migraine hangover." Brain and body recovering from the neurological event.
PBM potential
PBM's tissue repair and cellular recovery effects may support resolution of the residual neuroinflammation driving postdrome symptoms.
What the red and near-infrared light trials found
The most notable piece of clinical evidence here is a 2018 randomised controlled trial published in Arquivos de Neuropsiquiatria (Loeb et al., PMID 30427505). Thirty-six patients with chronic migraine were split into two groups - one received low-level laser therapy, the other received botulinum toxin A injections (Botox). Both groups kept pain diaries for 30 days before treatment, 30 days during, and 30 days after.
Both treatments reduced headache days, acute medication intake, and pain intensity. There was no statistically significant difference between them. Botox had the edge on reducing anxiety; laser therapy had the edge on reducing sleep disturbance. The authors concluded that both treatments are efficient against chronic migraine, with no difference between them in overall outcomes.
That finding deserves a moment. Botox for chronic migraine is a licensed, NICE-recommended treatment that costs several hundred pounds per round of injections and needs repeating every three months. Being comparable to it in a head-to-head RCT is not a small thing, even accounting for the study's limitations - 36 patients total, single-centre, clinical laser rather than home panel.
A 2022 systematic review registered on PROSPERO (CRD42021223429) pulled together the available RCTs on PBM for primary headache. Positive results appeared across included studies for both pain reduction and headache frequency, but the authors rated certainty of evidence as very low - mainly because the trials were small and properly blinding participants to light therapy is difficult. No adverse events were reported across any included study.
Separately, a 2024 paper in Scientific Reports (Campos et al., DOI 10.1038/s41598-024-82412-9) examined vascular photobiomodulation for tension-type headache and orofacial pain in post-COVID patients. PBM was applied over blood vessels rather than the head directly, and pain scores dropped significantly versus sham (p=0.010). A different delivery approach, but the same underlying mechanism.
What "very low certainty" actually means
When a systematic review rates certainty of evidence as very low, it does not mean the results are wrong or that the treatment doesn't work. It means the available studies are too small and variable for the review authors to be confident the effects will replicate consistently across a wider population. The results from the individual trials - including the Botox comparison - are real. What is missing is the large, multi-centre, well-powered RCT that would give the field higher confidence. That work is ongoing. The current evidence justifies cautious optimism, not dismissal and not overclaiming.
The green light story - and why it matters
While the red and NIR evidence works through tissue photobiomodulation - stimulating mitochondria, reducing inflammation, modulating pain signalling at the cellular level - green light operates through a completely different pathway. It works through the visual system itself.
Research from the University of Arizona, led by Dr Mohab Ibrahim, found that narrow-band green light exposure (approximately 520nm) significantly reduced migraine frequency and intensity in patients who had already failed multiple conventional treatments including Botox. In a crossover clinical trial of 29 patients, green light exposure for 1-2 hours daily resulted in roughly 60% reduction in both pain intensity during attacks and the number of migraine days per month. The effects appeared to be mediated through retinal pathways that connect to intrinsic pain-modulating systems in the brain - specifically the descending pain inhibition pathway via serotonin.
A 2025 RCT published in Brain Sciences (Mahmood et al., DOI 10.3390/brainsci15111209) compared green light therapy directly against transcranial direct current stimulation in migraine patients. After four weeks, 30% of participants in the green light group reported no migraine attacks at all, and the majority showed significant reductions in both frequency and duration. No serious adverse events occurred in either group.
A 2023 RCT in the Journal of Clinical Neuroscience (Posternack et al., PMID 37150129) tested the Avulux lens - a precision-tinted spectacle lens that blocks wavelengths known to exacerbate migraine pain while transmitting green light. Worn at the onset of a migraine, the lens significantly reduced pain intensity at both 2 and 4 hours post-onset compared to sham lenses, and reduced light sensitivity. Worth noting: two of the study authors have equity interests in Avulux, which is standard to flag when interpreting the results. This is green light being used as an acute treatment during an attack, not a preventive protocol - a different use case again.
Green light exposure is simple, inexpensive, and entirely non-invasive. Dedicated green LED strips or lamps are widely available and cheap. The Arizona research used 1-2 hours of daily exposure. One important clarification: this has nothing to do with a red light panel. NovaThera panels - and red light panels generally - emit red and near-infrared wavelengths, not green. The two approaches address migraines through completely different mechanisms and require completely different tools. A panel covers the red/NIR preventive evidence. For the green light protocol, you need a separate narrow-band green LED lamp. Both are worth considering; neither replaces the other.
Red/NIR vs green light - two different tools
Red and NIR panel
Preventive. Tissue-level. Applied to the head and neck.
Wavelengths: 630-670nm red and 810-850nm NIR
Targets: temples, forehead, back of neck - 10-20 min, several times weekly
Mechanism: neuroinflammation reduction, serotonin modulation, trigeminovascular pathway
Best evidence: RCT vs Botox, systematic review of PBM for primary headache
Green light exposure
Preventive and acute. Visual system. Ambient exposure.
Requires a dedicated narrow-band green LED lamp - not a red light panel.
Wavelength: narrow-band green ~520nm LED
Protocol: 1-2 hours daily ambient exposure in a dimly lit room
Mechanism: retinal photoreceptor pathways, descending serotonin pain inhibition - not tissue PBM
Best evidence: Arizona crossover study (60% reduction), 2025 Brain Sciences RCT, Avulux lens RCT
What this means if you have migraines
None of this supports replacing prescribed migraine treatment with light therapy. What it does support is treating light therapy as an adjunct - something that addresses mechanisms conventional treatments don't fully cover, with essentially no downside in terms of side effects.
For panel use, the protocol that makes most sense based on the clinical data is preventive: regular sessions on the upper face, temples, and back of the neck - the areas where the trigeminovascular and cervicogenic components of migraine originate. The Loeb study used clinical laser equipment, but the wavelengths (red and NIR) and the mechanisms they target are identical to what a full-body panel delivers. Ten to twenty minutes, several times a week, built into a consistent routine rather than used reactively when a migraine is already underway.
Green light is a different approach entirely - and not something a NovaThera panel delivers. You're not applying it to tissue; you're sitting in ambient green light for 1-2 hours a day. The Arizona protocol used narrow-band green LEDs at approximately 520nm in a dimly lit room. A dedicated green LED lamp is the right tool here, available cheaply online. It works through retinal pathways, not tissue photobiomodulation, and the two approaches address different parts of the migraine picture without overlapping.
Migraine management is personal in a way that few conditions match. What triggers one person's attacks doesn't trigger another's. Give any new approach enough time to evaluate - weeks, not a handful of sessions - and keep your neurologist or GP in the loop. None of this is a substitute for medical care.
When to talk to a doctor
If your migraines are frequent, severe, or significantly affecting your life and you are not currently under any kind of neurological or GP management for them, that conversation should happen before you start experimenting with any complementary approach. The same applies if you are pregnant, have a history of seizures, or are on multiple medications. Light therapy is low-risk, but migraine management is a medical topic and your care should be led by someone who knows your history.
Key takeaways
- A 2018 RCT found low-level laser therapy matched Botox for reducing headache days, pain intensity, and medication use in chronic migraine patients - with no significant difference between the two treatments.
- A systematic review of RCTs on PBM for primary headache found positive results but rated certainty as very low due to small study sizes. No adverse events were reported across any included trial.
- Green light therapy works through a completely different mechanism - via the visual system and serotonin pathways - and has separate strong evidence, including a 60% reduction in migraine frequency in a University of Arizona crossover study.
- Red and NIR panel use (preventive, regular sessions on temples and neck) and green light exposure (ambient, 1-2 hours daily from a dedicated green LED lamp) are different tools addressing different mechanisms. A NovaThera panel covers the red/NIR evidence; green light requires a separate lamp.
- The evidence justifies trying both as adjuncts to existing management. Give it weeks, not days, to evaluate. Keep your GP or neurologist aware of what you are doing.
Where this sits in the bigger picture
Migraines are one of those conditions where the gap between how debilitating they are and how well medicine addresses them remains frustratingly wide. The newer CGRP inhibitors are a real step forward, but they're not available to everyone and they don't work for everyone. For the majority of migraine sufferers who are navigating a patchwork of partially effective options, something safe with an actual evidence base and a negligible barrier to trying is worth knowing about.
Light therapy across both wavelengths clears that bar. The Botox comparison trial is a real and meaningful data point. The green light work from Arizona is hard to dismiss. The certainty of evidence needs to improve before anyone should be recommending this with the same confidence as a CGRP inhibitor - but that's a different question from whether it's worth trying as part of a broader approach. For most people with migraines, it probably is.
Sources
NovaThera
Built on verified science.
630-670nm red and 810-850nm NIR - the wavelengths used across the migraine and pain research literature. Published irradiance data, no overclaiming.