Status:
UNKNOWN
Efficacy of Mobile Neurofeedback for Adult Attention-Deficit/Hyperactivity Disorder (ADHD)
Lead Sponsor:
Sheba Medical Center
Collaborating Sponsors:
Myndlift Ltd.
Conditions:
Attention Deficit Hyperactivity Disorder
Eligibility:
All Genders
18-50 years
Phase:
NA
Brief Summary
This study is an assessor-blind, parallel-group, controlled trial to evaluate the benefit of home-based training with a low-cost, mobile neurofeedback system (Myndlift) in adults with ADHD. Randomized...
Eligibility Criteria
Inclusion
- willingness to provide consent
- diagnosis of Attention Deficit/Hyperactivity Disorder (ADHD) of any type as ascertained by clinical interview conducted by a board-certified psychiatrist
- at the time of enrollment, not receiving treatment for symptoms of ADHD
Exclusion
- comorbid psychotic or bipolar disorder or an active affective disorder
- medical disorder with potentially confounding psychiatric effects (either due to direct effects of the condition or medication effects)
- diagnosis of substance abuse disorder (SUD), sleep apnea, restless legs syndrome (RLS), or borderline intellectual functioning
- unable to attend in-clinic follow-up assessment
- antipsychotic agent in the three months prior to baseline assessment
- any selective serotonin reuptake inhibitor (SSRI) treatment in the four weeks prior to baseline
- other psychiatric medication in the two weeks prior to baseline that the principal investigator deems to be confounding
- experimental group only: plans to start stimulant medication during the course of the study (use of nutritional supplements including "prescription medical foods" is not exclusionary)
- neurofeedback treatment in the two years prior to baseline
Key Trial Info
Start Date :
December 22 2019
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
June 1 2021
Estimated Enrollment :
70 Patients enrolled
Trial Details
Trial ID
NCT04112082
Start Date
December 22 2019
End Date
June 1 2021
Last Update
October 2 2019
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