Tulsa, OK
Neurofeedback Therapy clinics in Tulsa
Neurofeedback therapy in Tulsa is offered at psychology practices, ADHD and autism clinics, and brain-performance centers, with neurology referrals often routed through Saint Francis Health, Ascension St John, and OSU Medical Center. Demand reflects an energy-industry and working-class patient base.
Neurofeedback uses EEG-based operant conditioning to train brain activity patterns, with variable evidence across ADHD, anxiety, PTSD, and post-concussion syndrome. It is FDA cleared as a biofeedback modality but not approved for specific psychiatric diagnoses. Clinics in Tulsa, Oklahoma vary in protocol (standard EEG, LORETA, qEEG-guided) and in whether they combine with psychotherapy. Oklahoma Medical Board rules on delegation and IV therapy shapes which professionals can deliver neurofeedback and bill insurance.
With neurofeedback clinics on Regenerated.com in Tulsa, patients can compare clinician credentials (licensed psychologist vs technician), qEEG mapping, and realistic outcome framing.
Dr. Sarah Washatka
- PRP Therapy
- Ozone Therapy
- IV Therapy
- Neurofeedback Therapy
- Hyperbaric Oxygen Therapy (HBOT)
IV Effect
- Ozone Therapy
- IV Therapy
- Neurofeedback Therapy
- Hyperbaric Oxygen Therapy (HBOT)
- Arthritis Treatment
Chiro Effect by Dr. Brandon Washatka
- NAD IV Therapy
- Vitamin IV Therapy
- PRP Therapy
- Ozone Therapy
- IV Therapy
Regulatory context
A note on Oklahoma's neurofeedback therapy rules.
Repetitive transcranial magnetic stimulation (rTMS) is regulated as a Class II prescription device. The first 510(k) clearance went to NeuroStar in 2008 for treatment-resistant major depressive disorder. Subsequent clearances expanded the on-label scope to obsessive-compulsive disorder (BrainsWay deep TMS, 2018), smoking cessation (BrainsWay, 2020), anxious depression as an adjunct indication (2021), and migraine via single-pulse TMS devices such as eNeura SpringTMS and SAVI Dual. Biofeedback instruments are cleared under 21 CFR 882.1425 as Class II devices for relaxation training and stress reduction. EEG-based neurofeedback systems hold 510(k) clearances in the same category. Cranial electrotherapy stimulation, tDCS wellness devices, and many vagus nerve stimulation accessories sold direct to consumers are not cleared as medical devices, and clinical claims beyond cleared indications are off-label.
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Oklahoma Medical Practice Act (59 O.S. 481 et seq.)
Defines the practice of medicine and supervision framework for delegated procedures including TMS technician work. -
Oklahoma Psychologists Licensing Act (59 O.S. 1351 et seq.)
Governs licensed psychologists who deliver biofeedback and neurofeedback within scope.
The Oklahoma State Board of Medical Licensure and Supervision investigates TMS clinics for supervision lapses and off-label marketing. The Oklahoma attorney general enforces the Oklahoma Consumer Protection Act against deceptive medical device advertising, including neurofeedback cure claims. Wellness clinics offering CES or tDCS face scrutiny when marketing implies FDA-cleared medical treatment. Commercial insurers and Oklahoma Medicaid SoonerCare typically require documented treatment-resistant depression before covering TMS for major depressive disorder.