Overview
What It Is Photobiomodulation uses red or near-infrared light delivered by lasers or LEDs to support cellular energy production and modulate inflammation. In neurological applications the light is typically applied to the scalp or forehead. Sessions last 10–30 minutes and are often given several times per week.
How It Works Light at specific wavelengths is absorbed by mitochondrial enzymes, which may increase cellular energy (ATP) and influence inflammatory and signaling pathways. In injured or under-functioning brain tissue, this is hypothesized to support a metabolic environment more conducive to repair and adaptive plasticity. Human evidence is still emerging.
Conditions - Studied for: traumatic brain injury and cognitive symptoms (small trials and pilots). - Also explored for: other neurological and mood applications. - Note: Larger rigorous studies are still limited. Temporary headache or fatigue can occur; overall risk is very low.
How it is administered
In-clinic sessions in which red or near-infrared light is applied to the scalp or forehead. Sessions often last 10–30 minutes and may be given 2–3 times per week for a course of weeks. Home devices are also used in some protocols.
Conditions connected in the NPA database
The NPA Treatment Database lists this treatment in connection with 10 condition records. A database relationship does not establish effectiveness, safety, or suitability for an individual.
Related questions
These controlled question pages reference this treatment through stored condition relationships.
- What treatments are listed for Alzheimer's Disease (AD) in the NPA database?
- What treatments are listed for Anxiety Disorders in the NPA database?
- What treatments are listed for Clinical Depression in the NPA database?
- What treatments are listed for Developmental Delays in the NPA database?
- What treatments are listed for Dyslexia & Learning Disabilities in the NPA database?
- What treatments are listed for Migraine & Headaches in the NPA database?
- What treatments are listed for Parkinson's Disease (PD) in the NPA database?
- What treatments are listed for Persistent Pain in the NPA database?
- What treatments are listed for Stroke in the NPA database?
- What treatments are listed for Traumatic Brain Injury (TBI) in the NPA database?
Symptoms connected in the NPA database
The current record associates this treatment with the following symptom information. This is not a claim that the treatment will improve these symptoms.
Cognition & Memory
- confusion with time/place
- Delayed cognitive skill development
- difficulty concentrating
- Difficulty concentrating (“brain fog”)
- difficulty with familiar tasks
- Difficulty with sequencing
- indecisiveness
- Later memory and thinking changes
- memory complaints
- Memory loss (especially recent events)
- mental fog
- mental fog during/after attacks
- processing speed for written information
- racing thoughts
- Short-term memory issues
- Short-term memory problems
- slowed mental processing
- slowed processing
- slowed thinking
- spatial neglect
- trouble planning or problem-solving
- working memory challenges
- worry
Emotion & Behavior
- anxiety
- apathy
- avoidance behaviors
- avoidance of reading tasks
- Depression
- difficulty with regulation
- emotional lability (uncontrollable laughing/crying)
- Excessive fear or worry
- feelings of worthlessness
- Frustration
- impulsivity
- irritability
- loss of interest/pleasure
- lowered self-confidence
- Mood and personality changes
- mood changes
- mood changes before or during attacks
- mood swings
- Persistent sadness
- social withdrawal
- Social-emotional delays
- withdrawal from activities
Motor Control
- Balance and coordination problems
- balance and gait problems
- Delayed gross or fine motor milestones
- difficulty walking
- guarding
- Later-stage mobility and coordination decline
- Minimal (occasional fine-motor or coordination differences)
- muscle stiffness/spasticity
- muscle tension
- Occasional weakness or coordination changes during aura (rare subtypes)
- One-sided weakness or paralysis
- poor balance and coordination
- reduced fine motor skills
- Reduced mobility
- Restlessness
- rigidity/stiffness
- slowed movement (bradykinesia)
- slowed movements
- Slowed movements or restlessness (psychomotor changes)
- trembling
- Tremor
- weakness
Sensory & Pain
- central post-stroke pain (burning, shooting pain, and sensitivity to touch, temperature)
- Generally minimal primary sensory changes
- headaches
- heightened sensitivity
- muscle aches
- nausea
- Numbness or altered sensation
- numbness or tingling
- Pain
- Persistent headaches
- Persistent pain (aching, burning, stabbing)
- Physical sensations (heart racing, chest tightness, sweating)
- reduced sense of smell
- sensitivity to light/noise
- sensitivity to light/sound/smell
- sensory changes
- Throbbing or pulsing head pain
- tinnitus
- Unexplained aches and pains
- Variable sensory processing differences
Sleep & Fatigue
- Excessive fatigue
- fatigue
- Insomnia or excessive sleepiness
- Insomnia or hypersomnia
- Mental fatigue from reading effort
- post-attack exhaustion
- profound fatigue and low energy
- profound physical and mental fatigue
- restlessness at night
- sleep disruption
- Sleep disruption due to pain
- sleep disturbances
- Sleep problems (including REM sleep behavior disorder)
- Trouble falling or staying asleep
- Variable sleep pattern issues
Visual & Auditory Processing
- Blurred or double vision
- Difficulty distinguishing letter/word shapes and sounds (core auditory-phonological and visual processing issues)
- difficulty judging distances or recognizing objects
- difficulty processing sounds
- difficulty processing visual information
- double vision
- Heightened sensitivity to sensory input in some cases
- light sensitivity
- phonophobia (sound sensitivity)
- Possible delays in visual-motor or auditory processing skills
- Spatial and visual perception problems
- Visual auras (flashes, zigzags, blind spots)
- Visual field loss
- Visual processing or spatial difficulties in some cases
Practical information
Insurance coverage
Rarely covered for TBI.
Cost information
$100–$300 per session; courses often $2,000–$6,000+.
Results and outcomes described in the source record
Some report benefits within a few sessions; more consistent changes often after 8–20 sessions.
Side effects and risks
Very low risk. Possible temporary headache or fatigue.
Research context in the NPA database
This section reproduces the current database's research summary and detail. Structured citation metadata has not been supplied, so it should not be read as an independently verified literature review.
Research summary
Evidence Level: Emerging
What the research shows: Small trials and pilot studies, especially in traumatic brain injury, report cognitive and symptom benefits. Larger rigorous studies are still limited.
Key takeaway: A low-risk light-based therapy being explored mainly for brain injury and some pain conditions; evidence is still developing.
Research detail
Overview Photobiomodulation uses red or near-infrared light delivered by lasers or LEDs to support cellular energy production (via mitochondrial cytochrome-c oxidase) and to modulate inflammation. In neurological applications the light is typically applied to the scalp or forehead. Sessions last 10–30 minutes and are often given two or three times per week for a course of weeks. Wavelength, power density, and placement are adjusted according to the clinical goal. Both clinic-based professional devices and home devices exist.
Evidence Base and Published Work • Small randomized controlled trials and pilot studies, especially in moderate traumatic brain injury (including Figueiro Longo et al., JAMA Network Open 2020), report cognitive and symptom benefits. • Pilot work by Naeser, Bogdanova and others, and systematic reviews note emerging but still limited rigorous evidence. • Key published work includes: – Figueiro Longo et al. (2020) and related small RCTs/pilot trials in moderate TBI. – Pilot work by Naeser and Bogdanova groups. – Systematic reviews noting emerging but still limited rigorous evidence. – Temporary headache or fatigue can occur; overall risk is very low. Evidence remains emerging.
Outcomes in small trials include cognitive and symptom benefits, especially in traumatic brain injury. Larger rigorous studies are still limited.
Questions to ask a provider
1. Is photobiomodulation appropriate for my cognitive or post-concussion symptoms, and what protocol (wavelength, dose, placement) do you use? 2. How many sessions are recommended, and over what timeframe? 3. What evidence exists for PBM in traumatic brain injury or cognitive symptoms, and what results are realistic? 4. Are there any risks or contraindications (e.g., photosensitivity, certain medications)? 5. Is this delivered only in clinic, or are home devices used, and what is the cost?
Website and contact information
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