Objective qEEG brain screening using the same FDA-referenced biomarker trusted by neurologists worldwide. Real brain data. Real normative comparison. A professional report your GP will take seriously. Use it for Right to Choose referrals, EHCP evidence, or Access to Work applications.
The primary FDA-referenced biomarker for ADHD. Measured at the central midline electrode — the exact site used in the NEBA system cleared by the FDA in 2013. An elevated theta/beta ratio at Cz indicates increased slow-wave activity relative to fast-wave activity, a pattern consistently observed in individuals with ADHD across decades of published research.
Secondary frontal midline measurement. Provides corroborating data from the frontal cortex, where executive function and attention are regulated. The frontal electrode site captures activity from the prefrontal cortex — the brain region most directly implicated in ADHD-related attention and impulse control difficulties.
Low frontal beta activity may indicate cortical hypoarousal — a well-documented neurological pattern associated with attention difficulties. Beta waves are the brain's "alert" frequency. When frontal beta power is significantly below normal, it suggests the brain's attention systems may not be activating as expected during tasks requiring sustained focus.
Complete band decomposition across delta, theta, alpha, beta, and gamma frequencies. Each band tells a different story about your brain's activity state. Delta dominance may suggest drowsiness or fatigue during recording, excessive alpha can indicate a disengaged state, and the overall spectral profile provides context for interpreting your theta/beta ratio results.
A computerised attention task measuring reaction time, omission errors (inattention), commission errors (impulsivity), and response variability. This behavioural task complements the EEG data by providing a direct measure of how well your brain sustains attention over a three-minute period, capturing the same difficulties that affect daily life, school performance, and workplace productivity.
Your results are compared against age-matched norms from 311+ research subjects. We show exactly how many standard deviations you fall from the healthy average. A z-score above 1.5 at electrode Cz is considered clinically significant for ADHD screening purposes, and our report presents this data in a clear visual format that clinicians can interpret immediately.
Choose your appointment. Fill in the intake form with basic details and presenting concerns beforehand. We offer same-week appointments at our Macclesfield clinic, with morning and afternoon slots available Monday to Saturday.
We place a lightweight cap with four medical-grade EEG sensors on your scalp. Setup takes around 5 minutes. Completely painless. The electrodes are positioned at international 10-20 system locations Cz, Fz, F3, and F4 — the exact montage used in published ADHD research studies.
Two minutes eyes open, two minutes eyes closed, and a three-minute Go/No-Go sustained attention task. Sit still, relax, and let your brain do the talking. Children can sit with a parent present throughout, and we take breaks if needed. The recording environment is quiet and calm.
You receive a professional PDF report the same day with your TBR, z-scores, attention task results, and normative comparison. Ready for your GP, psychiatrist, or school SENCO. See the full process.
Attention deficit hyperactivity disorder (ADHD) is a neurodevelopmental condition characterised by persistent patterns of inattention, hyperactivity, and impulsivity that interfere with daily functioning. According to the NICE clinical guidelines (NG87), ADHD affects approximately 3–5% of children and 2–4% of adults in the UK, though recent studies suggest prevalence may be higher than previously estimated, particularly among women and girls who are systematically underdiagnosed.
ADHD is not a behavioural choice or a parenting issue. It is a neurological condition with measurable differences in brain function. Research consistently shows that individuals with ADHD have altered patterns of electrical brain activity, particularly in the frontal and central regions responsible for executive function, sustained attention, working memory, and impulse control. These differences are detectable through quantitative electroencephalography (qEEG) — the technology we use in our screening service.
ADHD presents differently in different people. The NHS describes three main presentations: predominantly inattentive (difficulty sustaining focus, easily distracted, forgetful in daily activities), predominantly hyperactive-impulsive (fidgeting, difficulty staying seated, excessive talking, acting without thinking), and combined presentation (features of both). Inattentive ADHD is particularly common in women and girls, and because it lacks the visible hyperactivity that teachers and parents notice, it is frequently missed entirely. Many adults seeking our screening have spent years wondering why they struggle with organisation, time management, and focus despite being intelligent and capable. Our qEEG screening does not distinguish between subtypes, but the theta/beta ratio pattern is consistently elevated across all three presentations, making it a useful objective data point regardless of which type of ADHD is suspected.
The standard route to an ADHD assessment in the UK typically involves a GP referral to a community mental health team, CAMHS (for children), or a specialist adult ADHD service. Average NHS waiting times now exceed two to five years in many areas, with some regions reporting waits of seven years or more. During this wait, children may fall behind academically, adults may struggle at work, and families experience significant stress without any formal support or reasonable adjustments.
When an assessment does eventually happen, it relies almost entirely on subjective measures: clinical interviews, behavioural questionnaires (such as the Conners Rating Scale, DIVA-5, or QB Test), school or workplace observations, and developmental history gathered from parents or partners. These tools are clinically valid and form the backbone of ADHD assessment worldwide, but they are inherently subjective — dependent on self-reporting accuracy, observer bias, the clinician's experience, and how the individual presents on that particular day. There is no standard brain measurement in the conventional NHS ADHD pathway, which is where our service fills a gap.
A quantitative EEG measures brain activity directly. The theta/beta ratio — the ratio between slow-wave (theta, 4–8 Hz) and fast-wave (beta, 13–30 Hz) activity at the central midline — is a well-established neurological marker that has been studied extensively since the 1990s. Individuals with ADHD consistently show elevated theta relative to beta, reflecting cortical underarousal in the prefrontal regions responsible for attention and executive function. In simple terms, the brain's "idle" waves are too dominant relative to its "alert" waves, particularly in the parts of the brain that control focus and self-regulation.
Unlike questionnaires, EEG data cannot be influenced by mood, motivation, social desirability bias, or how a person happens to feel on the day. It provides a quantitative measurement that can be compared against normative databases of healthy controls, producing a z-score that tells you exactly how far from the population average your brain activity falls. This is the same approach that led to the FDA's clearance of the NEBA System in 2013 as a diagnostic aid for ADHD in children and adolescents aged 6–17.
An MRI shows brain structure — the physical anatomy and white matter pathways. An fMRI shows blood oxygen level dependent (BOLD) signals associated with brain activity over several seconds. A CT scan uses ionising radiation to image brain tissue. None of these modalities are routinely used for ADHD assessment because they do not measure the millisecond-resolution electrical timing patterns that distinguish ADHD brains from neurotypical brains. A qEEG measures electrical brain wave patterns in real time with millisecond precision, capturing the exact cortical arousal patterns that decades of ADHD research have identified as neurological markers. It is also entirely non-invasive, takes only seven minutes of recording time, requires no radiation or contrast agents, produces no side effects, and is suitable for children as young as six years old. This combination of clinical relevance, safety, speed, and objectivity makes qEEG uniquely suited to ADHD screening.
The theta/beta ratio (TBR) has been studied in over 1,770 ADHD subjects across multiple peer-reviewed meta-analyses. In 2013, the FDA cleared the NEBA System as a diagnostic aid using this exact biomarker at electrode Cz.
Our normative database is compiled from six published research sources including Arns et al. (2013), Monastra et al. (1999), Clarke et al. (2001), and Ogrim et al. (2012), supplemented by our own computed norms from 311 real subjects across the Mendeley and IEEE open-access datasets.
The American Academy of Neurology reports an accuracy of 89–94% when TBR is combined with clinical evaluation. For clinical context, see the NICE ADHD guidelines (NG87) and the NHS ADHD overview.
The report is structured to provide both the raw data and the clinical context needed for a healthcare professional to interpret your results. It begins with a summary of your presenting concerns and the screening protocol used, followed by the core metrics: your theta/beta ratio at electrodes Cz and Fz, expressed as both absolute values and z-scores against our published normative database of 311+ subjects. The z-score tells your clinician exactly how many standard deviations your brain activity falls from the age-matched healthy average — a universally understood statistical measure.
The report includes a full frequency band decomposition showing your relative power across delta (1–4 Hz), theta (4–8 Hz), alpha (8–13 Hz), beta (13–30 Hz), and gamma (30–45 Hz) frequency bands, presented as both raw power spectral density values and percentage distributions. This complete spectral profile provides additional context — for example, elevated alpha may suggest the subject was disengaged during recording, while elevated delta may indicate drowsiness.
Your Go/No-Go sustained attention task results are presented separately, covering four key metrics: mean reaction time (how quickly you respond to targets), omission errors (targets you missed, indicating inattention), commission errors (responses to non-targets, indicating impulsivity), and reaction time variability (inconsistency in response speed, a hallmark of ADHD-related attention fluctuation). Each metric is compared against age-appropriate norms.
The report concludes with a clinical context section that cites the relevant peer-reviewed literature, explains the significance of your results in the context of published ADHD research, and provides clear guidance on recommended next steps. This may include presenting the report to your GP to support a referral, using it as evidence for a Right to Choose application, providing it to a private psychiatrist as supplementary data, or submitting it to your child's school as part of an EHCP application. Our GP appointment guide includes suggested scripts for presenting your results to a doctor who may not be familiar with qEEG technology.
Tired of waiting years on the NHS waiting list? Get objective brain data now that your GP can use to expedite a referral or support a private assessment. See our parent's guide for school support, EHCP and exam access.
Wondering if your difficulty concentrating is ADHD or something else? Our screening provides an objective neurological data point — not just another questionnaire. Women are underdiagnosed by a factor of 2:1. After your screening, our support hub guides you through next steps and GP appointments.
Support EHCP applications and SEN assessments with objective neurological evidence. Our reports are used by SENCOs across the North West to strengthen applications and demonstrate clinical need. Bulk pricing available for educational institutions.
Supplement your clinical evaluation with quantitative EEG data. Our reports include z-scores, normative comparisons, and peer-reviewed citations. Many GPs find the objective data helps strengthen referral letters and supports faster processing through CAMHS and adult assessment pathways.
Already on ADHD medication? A pre/post brain scan shows objective changes in brain activity — evidence that your treatment is working, or that an adjustment may be needed. Read our medication guide or book a medication comparison scan.
Need objective evidence for workplace adjustments, Access to Work applications, disability tribunal support, or insurance purposes? Our reports provide citable neurological data with z-scores and normative comparisons. See your full ADHD workplace rights.
Certified EEG technician with hands-on experience conducting over 200 qEEG screenings for children, adolescents, and adults. Our screening protocol is based on the FDA-cleared NEBA System methodology (2013) and normative data compiled from six published peer-reviewed research sources spanning over two decades of ADHD neuroscience. All reports follow established clinical guidelines and are designed for use by GPs, psychiatrists, CAMHS teams, and educational psychologists.
Last reviewed: April 2026 · Sources cited: Arns et al. (2013), Monastra et al. (1999), FDA NEBA Clearance, NICE NG87
A quantitative EEG (qEEG) measures the electrical activity of your brain using sensors placed on your scalp. It is completely non-invasive — no needles, no radiation, no discomfort. We analyse the patterns in your brain waves, specifically the ratio between theta and beta frequencies, which is an FDA-referenced biomarker for ADHD. The theta/beta ratio reflects the balance between your brain's resting-state activity and its alertness activity, and elevated ratios have been consistently documented in individuals with ADHD across thousands of published research subjects.
No. This is an objective brain screening that provides quantitative data to support or inform a clinical evaluation. ADHD diagnosis requires a comprehensive assessment by a qualified clinician including clinical interview, behavioural rating scales, and developmental history. Our report is designed as additional objective evidence to present to your GP or psychiatrist — it adds a neurological data point to the clinical picture that traditional assessments do not provide.
The American Academy of Neurology reports an accuracy of 89–94% when the theta/beta ratio is combined with clinical evaluation. As a standalone measure, sensitivity is approximately 58% and specificity 74%. This is why we provide it as supporting data for a clinician's assessment, not as a standalone diagnostic tool. The value of the qEEG lies in providing objective neurological evidence that complements the subjective measures used in traditional ADHD assessment, giving clinicians a more complete picture.
We screen children aged 6 and above, adolescents, and adults of all ages. Our normative database includes age-matched reference data for 10 different age groups from 6–7 years through to 60+, sourced from published peer-reviewed research. We use age-specific norms to ensure your results are compared against an appropriate reference population — a 7-year-old is not compared against adult norms, and vice versa.
Our reports include peer-reviewed citations, z-scores against published normative data, and clear clinical context. They are designed to provide objective supplementary data that a GP or psychiatrist can use alongside their own clinical evaluation. Many clinicians welcome additional neurological data to support their assessments and strengthen referral letters. Our GP appointment guide includes suggested scripts for presenting your results effectively.
A private ADHD assessment (£700–£1,500) typically involves a conversation with a psychiatrist using questionnaires and clinical interview — no brain measurement. We provide something they do not: actual objective brain data. Many clients use our screening before or alongside their private assessment. Some use it to build evidence for an NHS referral, others present it to a private psychiatrist as additional neurological evidence, and some use it for Right to Choose applications.
Wash your hair on the day (no heavy products or oils). Avoid excessive caffeine on the morning of the test. If taking ADHD medication, discuss with your clinician whether to take it before the screening — we can scan both on and off medication for comparison. For children, we recommend scheduling at a time when they are likely to be calm and cooperative. Saturday morning appointments are popular with families for this reason.
We are based in Macclesfield, Cheshire — easily accessible from Manchester (30 minutes), Stockport (20 minutes), Wilmslow, Knutsford, and the wider North West. Free parking is available. We also offer clinic sessions at selected locations across the region. Families travel from across the North West and Midlands for our service.
The full screening protocol takes approximately 30 minutes from arrival to completion. The actual recording is seven minutes: two minutes eyes-open resting EEG, two minutes eyes-closed resting EEG, and three minutes of a Go/No-Go sustained attention task. Setup of the electrode cap adds approximately 5–10 minutes, and we allow a few minutes for your child or yourself to settle comfortably before recording begins. Your report is delivered the same day by email as a professional PDF.
Yes. Our qEEG report provides objective neurological evidence that can strengthen a Right to Choose referral to a private ADHD provider such as Psychiatry-UK or Clinical Partners. Many clients use our report alongside their GP referral letter to demonstrate clinical need for assessment, particularly when NHS waiting times are prohibitively long. The report provides the kind of objective evidence that supports a compelling case for expedited assessment under the Right to Choose framework.
An MRI shows brain structure. An fMRI shows blood flow patterns associated with brain activity. Neither measures the millisecond-resolution electrical timing patterns that distinguish ADHD brains from neurotypical brains. A qEEG measures electrical brain wave patterns in real time with millisecond precision, making it uniquely suited to detecting the cortical underarousal pattern associated with ADHD. It is also non-invasive, fast (seven minutes of recording), requires no radiation or contrast agents, and is suitable for children as young as 6. This is why the FDA chose EEG-based technology for its first-ever approved ADHD diagnostic aid.
A 60-second look at the ADHD brain screening experience.
Book your ADHD brain screening today. Same-week appointments available.
Book your screening →Important: ADHD Brain Scan UK provides objective qEEG brain screening data. This is not a medical diagnosis. ADHD diagnosis requires a comprehensive clinical assessment by a qualified healthcare professional including clinical interview, behavioural observation, and developmental history. Our reports are designed as supplementary evidence to support — not replace — professional clinical evaluation. Always consult your GP or a qualified psychiatrist before making healthcare decisions. Read our full disclaimer.