See the article here: Neurofeedback and standard pharmacological intervention in ADHD: A randomized controlled trial with six-month follow-up
Disclaimer: The content below was generated with the assistance of AI and then reviewed and edited by BrainMaster Technologies, Inc. It is provided for educational and informational purposes only and does not constitute medical advice.
Overview #
This randomized controlled trial compared EEG-based neurofeedback (NF) with standard methylphenidate treatment in children with ADHD. A total of 23 children (ages 7–14) were assigned to either 40 sessions of theta/beta neurofeedback using BrainMaster Atlantis II or to standard pharmacological care. Follow-ups were conducted at 2 months and 6 months.
1. Study Purpose #
The study aimed to determine whether neurofeedback produces improvements comparable to stimulant medication in reducing ADHD symptoms and functional impairments over time. It is the first RCT to include a 6-month naturalistic follow-up for both interventions.
2. Methods #
Participants #
Final sample: 23 children (12 NF, 11 medication)
Diagnosis: ADHD per DSM-IV; no major comorbidities except ODD
IQ: All participants had an IQ higher than 80
Setting: University of Balearic Islands and Son Llatzer Hospital
Interventions #
Neurofeedback Protocol #
Equipment: Atlantis II 2×2, BrainMaster Technologies
Protocol: Theta (4–7 Hz) inhibition & Beta (15–20 Hz) enhancement
Electrode sites: Cz (younger children) or FCz (older participants)
Sessions: 40 total; two per week; ~35 minutes each
Reinforcement: Adaptive thresholds, visual & auditory feedback
Pharmacological Treatment #
Medication: Methylphenidate (approx. 1 mg/kg/day)
Ongoing use: Continued through post-assessment and follow-ups
Outcome Measures #
Collected from mothers, fathers, teachers, and parents (WFIRS):
ADHD-RS (Inattention, Hyperactivity/Impulsivity)
Oppositional Defiant Disorder Scale (ODD)
Weiss Functional Impairment Rating Scale (WFIRS)
Academic performance (teacher-rated, 5 domains)
3. Key Findings #
3.1 Symptom Reduction #
Both neurofeedback and medication led to significant reductions in:
Inattention
Hyperactivity/Impulsivity
Overall ADHD-RS scores
Functional impairment (WFIRS)
These improvements were comparable across groups at most timepoints.
Figures and tables (e.g., Table 3, Figure 3) show parallel improvement trajectories.
3.2 Academic Performance #
A major differentiator:
Only the Neurofeedback group showed significant improvements in: #
Reading
Reading comprehension
Writing
Later gains in math at follow-up
(See Table 4 & Table 5 for effect sizes.)
The medication group did not demonstrate significant academic gains.
3.3 Long-Term Outcomes #
2-Month Follow-Up #
NF group largely maintained gains without ongoing NF
Some NF participants began medication, but excluding them did not change results
6-Month Follow-Up #
Improvements generally maintained in both groups
One-third of NF participants required no additional treatment at 6 months
Mixed NF+medication effects limit interpretation at this timepoint
4. Strengths & Limitations #
Strengths #
Randomized controlled design
Two follow-up periods
Multi-informant (parents + teachers) evaluation
Detailed academic performance assessment
Use of standardized BrainMaster NF hardware
Limitations #
Small sample size (n=23)
Naturalistic follow-up (some NF participants began medication)
No neurophysiological results included in this paper
No specific transfer/generalization training within NF protocol
5. Conclusions #
Neurofeedback and medication produced similar reductions in core ADHD symptoms.
Neurofeedback uniquely supported academic performance improvements.
NF benefits persisted for months after training, even without continued NF sessions.
NF may serve as a valuable non-pharmacological or complementary option for ADHD clinical management.
(Full details in Highlights section on p.38.)
