Personalized at-home neurofeedback compared with long-acting methylphenidate in an european non-inferiority randomized trial in children with ADHD

被引:20
|
作者
Bioulac, Stephanie [1 ,2 ,3 ]
Purper-Ouakil, Diane [4 ]
Ross, Tomas [5 ]
Blasco-Fontecilla, Hilario [6 ,7 ]
Prats, Marie [8 ]
Mayaud, Louis [8 ]
Brandeis, Daniel [9 ,10 ,11 ]
机构
[1] CHU Pellegrin, Clin Sommeil, F-33076 Bordeaux, France
[2] Univ Bordeaux, Sommeil Addict & Neuropsychiat, USR 3413, F-33000 Bordeaux, France
[3] CNRS, SANPSY, USR 3413, F-33000 Bordeaux, France
[4] CHU Montpellier St Eloi Hosp, Unit Child & Adolescent Psychiat MPEA1, Montpellier, France
[5] Univ Geneva, Dept Neurosci, Lab Neurol & Imaging Cognit, Geneva, Switzerland
[6] Puerta de Hierro Univ Hosp, Segovia de Arana Hlth Res Inst IDIPHISA, Dept Psychiat, Ave Manuel Falla S-N, Madrid, Spain
[7] Univ Autonoma Madrid, Madrid, Spain
[8] Mensia Technol, 130 Rue Lourmel, F-75015 Paris, France
[9] Univ Zurich, Zurich, Switzerland
[10] Swiss Fed Inst Technol, Neurosci Ctr Zurich, Zurich, Switzerland
[11] Heidelberg Univ, Cent Inst Mental Hlth, Dept Child & Adolescent Psychiat & Psychotherapy, Med Fac Mannheim, Mannheim, Germany
关键词
Attention deficit hyperactivity disorder; Neurofeedback; Methylphenidate; Clinical trial; ATTENTION-DEFICIT/HYPERACTIVITY DISORDER; DEFICIT HYPERACTIVITY DISORDER; DIFFICULTIES QUESTIONNAIRE; VALIDITY; SCALE; EEG; BRAIN; CONSISTENCY; ANNOTATION; VALIDATION;
D O I
10.1186/s12888-019-2218-0
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
BackgroundNeurofeedback (NF) has gained increasing interest among non-pharmacological treatments for Attention Deficit Hyperactivity Disorder (ADHD). NF training aims to enhance self-regulation of brain activities. The goal of the NEWROFEED study is to assess the efficacy of a new personalized NF training device, using two different protocols according to each child's electroencephalographic pattern, and designed for use at home. This study is a non-inferiority trial comparing NF to methylphenidate.MethodsThe study is a prospective, multicentre, randomized, reference drug-controlled trial. One hundred seventy-nine children with ADHD, aged 7 to 13years will be recruited in 13 clinical centres from 5 European countries. Subjects will be randomized to two groups: NF group (Neurofeedback Training Group) and MPH group (Methylphenidate group). Outcome measures include clinicians, parents and teachers' assessments, attention measures and quantitative EEG (qEEG). Patients undergo eight visits over a three-month period: pre-inclusion visit, inclusion visit, 4 discovery (NF group) or titration visits (MPH group), an intermediate and a final visit. Patients will be randomized to either the MPH or NF group. Children in the NF group will undergo either an SMR or a Theta/Beta training protocol according to their baselineTheta/Beta Ratio obtained from the qEEG.DiscussionThis is the first non-inferiority study between a personalized NF device and pharmacological treatment. Innovative aspects of Mensia Koala (TM) include the personalization of the training protocol according to initial qEEG characteristics (SMR or Theta/Beta training protocols) and an improved accessibility of NF due to the opportunity to train at home with monitoring by the clinician through a dedicated web portal.Trial registrationNCT02778360. Date registration (retrospectively registered): 5-12-2016. Registered May 19, 2016
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页数:13
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