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Neurofeedback: What Research Shows

What randomized trials and meta-analyses show about neurofeedback for ADHD and other uses, why blinded ratings matter, and what the device rules do and do not say.

Content last updated . This page has not been medically reviewed.

What neurofeedback is

Neurofeedback is a form of biofeedback that uses brain activity. A sensor, most often an electroencephalogram (EEG) on the scalp, records the signal. A screen or sound then shows the person how that signal is changing, and the person practices shifting it. In the United States, the Food and Drug Administration (FDA) describes a biofeedback device in general terms as an instrument that provides a visual or auditory signal so that a person can consciously adjust certain body measures. [1]

This page covers the research evidence. For consumer headbands that only record signals, see consumer EEG devices. For the wider research setting, see neurofeedback research context.

ADHD: the best-studied use

Label: mixed, with no clear benefit on blinded ratings.
  • A 2025 meta-analysis in JAMA Psychiatry pooled 38 randomized trials (2,472 participants aged 5 to 40). On probably blinded reports of ADHD symptoms there was no significant improvement. The authors concluded that neurofeedback did not appear to meaningfully benefit people with ADHD, clinically or neuropsychologically, at the group level. [2]
  • An earlier 2016 meta-analysis found benefits only on ratings by people closest to the treatment, who were the least blinded. Effects were not significant with probably blinded ratings or in trials with active or sham controls. Only 4 studies checked directly whether participants had learned to change their brain signal. [3]
  • A 2013 review reached the same pattern: effects shrank to nonsignificant when the best probably blinded assessment was used. [4]
  • A 2022 meta-analysis found improvement in sustained attention on laboratory tests (Hedges' g = 0.32). That effect was much smaller (g = 0.05) when only studies that blinded participants were included. [5]
  • A sham-controlled trial of a scanner-based version (fMRI neurofeedback) in 88 boys with ADHD found no significant group difference on the main symptom scale. [6]
  • In adults with ADHD, a 2025 network meta-analysis found that the effects of non-pharmacological strategies were inconsistent across different raters. [7]

Why blinding matters: when parents, teachers or participants know a treatment is being given, they may expect improvement and rate it that way. Sham-controlled and blinded designs help separate the training itself from expectation. See placebo and expectancy effects.

Other uses

  • Tourette syndrome. A small double-blind, sham-controlled crossover trial of scanner-based neurofeedback in 21 adolescents found a greater tic reduction after real than sham feedback. [8] This is promising but limited: it was a small study, it used a research scanner rather than a consumer headset, and it does not show that home devices work.
  • Sport and performance. An umbrella review of psychological skills training for sport (which included neurofeedback among many approaches) reported that most findings were weak or non-significant and certainty was generally very low. [9] Label: insufficient evidence.
  • Sleep, anxiety, depression, focus, "peak performance". Proper evidence not found. The PubMed searches I ran for neurofeedback did not turn up a readable review or sham-controlled trial for these uses, so no claim is made.

What device rules do and do not mean

FDA's regulation for biofeedback devices places them in Class II (special controls) and exempts prescription, battery-powered units for relaxation and muscle retraining from premarket notification. [1] That describes the device category. It is not an FDA finding that neurofeedback treats ADHD, and a sold product's intended use matters. Accuracy of a device and benefit of training are separate questions.

How to judge a neurofeedback claim

  1. Which condition and age group were studied?
  2. Was there a sham or active comparison, and were raters blinded?
  3. Did the study show participants learned to change the signal, and did real-world symptoms change?
  4. Is the "brain training" claim a clinical outcome, or only a change in a brain signal? See clinical outcomes vs brain-signal changes.

Frequently asked questions

Does neurofeedback work for ADHD?

Pooled results of randomized trials are mixed. A 2025 meta-analysis found no significant improvement on probably blinded symptom reports and concluded there was no meaningful group-level benefit. [2]

Why do some studies show benefit and others do not?

Effects tended to appear in ratings by people who knew the treatment was given, and to shrink with blinded ratings or sham controls. [3]

Is neurofeedback FDA approved?

FDA regulates biofeedback devices as a category (Class II, with some exemptions). [1] I did not verify device-specific clearances or indications for neurofeedback products, so this page makes no claim about any one product.

Can neurofeedback help sleep, anxiety or focus in healthy people?

Proper evidence not found in the sources I could read. Do not rely on marketing claims for these uses.

Is it safe?

I did not find a safety review I could read this session, so no safety claim is made. Ask the clinician about your own health history first.

More details: evidence, limits and cautions

The details behind this page: cautions, limits of the evidence and where sources disagree. Open any note to read it.

How to read the evidence labels

Labels used on this page: promising but limited, mixed, insufficient evidence, no good evidence of benefit, and marketing claim. A "probably blinded" rating means the person scoring symptoms was probably unaware of which treatment the participant received.

Who should check first
  • Anyone considering neurofeedback in place of an ADHD evaluation or treatment already prescribed. Do not stop or change a medicine without the prescriber. See ADHD in adults and talking with a health professional.
  • Parents weighing multi-week programs: ask what outcome will be measured, who will rate it, and whether the rater will know the treatment.
  • People with seizures or a psychiatric condition: raise it with the clinician first.
References
  1. 21 CFR 882.5050, Biofeedback device (Cornell Legal Information Institute copy of the Code of Federal Regulations). Read 2026-10-22.
  2. Neurofeedback for Attention-Deficit/Hyperactivity Disorder: A Systematic Review and Meta-Analysis. JAMA Psychiatry 2025. Read 2026-10-22.
  3. Neurofeedback for ADHD: Meta-Analysis of Clinical and Neuropsychological Outcomes From Randomized Controlled Trials. J Am Acad Child Adolesc Psychiatry 2016. Read 2026-10-22.
  4. Nonpharmacological interventions for ADHD: systematic review and meta-analyses of randomized controlled trials of dietary and psychological treatments. Am J Psychiatry 2013. Read 2026-10-22.
  5. Surface electroencephalographic neurofeedback improves sustained attention in ADHD: a meta-analysis of randomized controlled trials. Child Adolesc Psychiatry Ment Health 2022. Read 2026-10-22.
  6. Double-Blind, Sham-Controlled Randomized Trial Testing the Efficacy of fMRI Neurofeedback on Clinical and Cognitive Measures in Children With ADHD. Am J Psychiatry 2022. Read 2026-10-22.
  7. Comparative efficacy and acceptability of pharmacological, psychological, and neurostimulatory interventions for ADHD in adults: a systematic review and component network meta-analysis. Lancet Psychiatry 2025. Read 2026-10-22.
  8. Randomized, Sham-Controlled Trial of Real-Time Functional Magnetic Resonance Imaging Neurofeedback for Tics in Adolescents With Tourette Syndrome. Biol Psychiatry 2020. Read 2026-10-22.
  9. Psychological skills training for sport-related outcomes: An umbrella review of evidence credibility and methodological quality. J Sports Sci 2026. Read 2026-10-22.
Education, not medical advice. This page is for general information. It does not diagnose or treat any condition and is not a substitute for care from a qualified health professional. Natural does not automatically mean safe. Ask a clinician or pharmacist before changing your care, especially if you take medication, are pregnant or breastfeeding, or have a health condition.