Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT02251743 · ClinicalTrials.gov registry record · NA

Double-Blind 2-Site Randomized Clinical Trial of Neurofeedback for ADHD

A NA study, sponsored by Ohio State University.

Completed
Registry status
NA
Development phase
144
Enrollment target

NCT02251743: Completed NA study, sponsored by Ohio State University.

NCT02251743 is a NA study that has completed, run by Ohio State University. The registered enrollment target is 144 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (90% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT02251743, a NA study, has completed, sponsored by Ohio State University.

COMPLETED
Registry status
NA
Development phase
144 participants
Enrollment target

Study Summary

Additional treatments with long-term benefit for attention-deficit/hyperactivity disorder (ADHD) are needed; one of the more promising is neurofeedback (EEG biofeedback), which has several randomized controlled trials showing significant benefit, but which are inconclusive because they were not double-blinded; the benefit could have been nonspecific (placebo response). Because of neurofeedback's labor-intensive cost (1 treatment costing as much as a month's medication), It is important to know how much specific benefit it yields. This 2- site placebo-controlled double-blind randomized clinical trial is the first to test for a specific benefit of neurofeedback with adequate power, the first designed and implemented collaboratively by experts in neurofeedback, ADHD, and clinical trials, the first to rigorously monitor quality not only of treatment, but also of placebo and blinding, and the first to follow up for 2 years to examine enduring effect; the results, whether positive or negative, will provide evidence for clinical practice and public policy regarding ADHD.

Primary Outcome

The primary outcome measure is the composite scores of teacher and parent-rated inattentive symptoms on the Conners-3, rated on a scale of 0-3. Lower scores represent a better outcome, with a maximum score of 3 and a minimum score of 0.

Interventions

  • DEVICE Neurofeedback treatment

Trial Details

FieldValue
Enrollment Target 144 participants
Start Date 2014-09
Est. Completion 2020-08
Phase NA
Ohio State University

552 total trials

What the finished NCT02251743 record still lists

NCT02251743 is an interventional study that assigns participants to a tested intervention. The registered 144 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (90% lower).

The record links to 0 conditions, and to 1 intervention - of which Neurofeedback treatment is the first listed.

NCT02251743 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02251743 about?

NCT02251743 is a clinical study titled "Double-Blind 2-Site Randomized Clinical Trial of Neurofeedback for ADHD". Additional treatments with long-term benefit for attention-deficit/hyperactivity disorder (ADHD) are needed; one of the more promising is neurofeedback (EEG biofeedback), which has several randomized controlled trials showing significant benefit, but which are inconclusive because they were not doub...

What is the current status of trial NCT02251743?

This trial is currently completed. It is a NA study. The enrollment target is 144 participants. The study started on 2014-09. Estimated completion is 2020-08.

What interventions are being tested in trial NCT02251743?

The interventions under investigation include: Neurofeedback treatment (DEVICE).

Who is sponsoring clinical trial NCT02251743?

This trial is sponsored by Ohio State University, which has 552 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02251743's enrollment target sits among peer trials

144 706th of 2000 higher than 1,290 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT01861106 · 144 participants · Phase 2

    Allogeneic Hematopoietic Stem Cell Transplant for GATA2 Mutations

  • NCT03482245 · 144 participants · NA

    The Role of Circadian Clock Proteins in Innate and Adaptive Immunity

  • NCT03504683 · 144 participants · NA

    MEAL TIMING Study: Effect of Time-Restricted Feeding on 24-hour Glycemic Control, Blood Pressure, and Cardiovascular Disease Risk Factors in Adults With Prediabetes

  • NCT03905603 · 144 participants · Early Phase 1

    Relative Contributions of Predictors of Hyperandrogenism in Older vs. Young Women With PCOS

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT02251743, the US trial registry maintained by the National Library of Medicine. NCT02251743 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.