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Effects of EEG- Microstate Neurofeedback on Attention and Impulsivity in Adult Attention-deficit/Hyperactivity Disorder (ADHD) and Neurotypical Controls (ADHDmicroNFB)

Primary Purpose

ADHD, Healthy

Status
Recruiting
Phase
Not Applicable
Locations
Switzerland
Study Type
Interventional
Intervention
Neurofeedback
Sponsored by
Nader Perroud
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for ADHD

Eligibility Criteria

18 Years - 50 Years (Adult)All SexesAccepts Healthy Volunteers

ADHD POPULATION GROUP

A subject will be eligible if all the following criteria apply:

  • Age: between 18-50 years
  • Gender: male and female
  • Health: general good health and normal or corrected-to-normal visual acuity
  • Patients clinically able to stop the following psychotropic medications for 48h: psychostimulants, benzodiazepines
  • Having provided written informed written consent

A subject will not be eligible if any of the following criteria apply:

  • Past or current history of a clinically significant central nervous system disorder, including structural brain abnormalities; cerebrovascular disease; history of other neurological disease, epilepsy, stroke or head trauma (defined as loss of consciousness > 5 min or requiring hospitalization)
  • Impaired vision (normal or corrected acuity below 20/40)
  • Medical illness (e.g., cardiovascular disease, renal failure, hepatic dysfunction)
  • Comorbidities with current psychiatric disorders (bipolar disorder, borderline personality disorder, major depressive disorder, anxiety disorder) including substance use disorder as defined by the DIGS.

HEALTHY POPULATION GROUP

A subject will be eligible if all of the following criteria apply:

  • Age: between 18-50 years
  • Gender: male and female
  • Health: general good health and normal or corrected-to-normal visual acuity
  • Having provided written informed written consent

A subject will not be eligible if any of the following criteria apply:

  • Past or current history of ADHD
  • Past or current history of main psychiatric disorders (bipolar disorder, borderline personality disorder, major depressive disorder, anxiety disorder), including substance use disorder as defined by the DIGS.
  • Past or current history of a clinically significant central nervous system disorder, including structural brain abnormalities; cerebrovascular disease; history of other neurological disease, including epilepsy, stroke or head trauma (defined as loss of consciousness > 5 min or requiring hospitalization)
  • Impaired vision (normal or corrected acuity below 20/40)
  • Medical illness (e.g., cardiovascular disease, renal failure, hepatic dysfunction)

Sites / Locations

  • TRE Unit (Trouble de la Régulation Emotionnelle) Department of psychiatry, HUGRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

healthy population group

ADHD population group

Arm Description

The experimental design includes three sessions: session 1 will be used to evaluate diagnostic using different targeted questionnaires. sessions 2 and 3 will be decomposed into 3 consecutives parts: Pre evaluation Neurofeedback Post evaluation

The experimental design includes three sessions: session 1 will be used to evaluate diagnostic using different targeted questionnaires. sessions 2 and 3 will be decomposed into 3 consecutives parts: Pre evaluation Neurofeedback Post evaluation

Outcomes

Primary Outcome Measures

Change in microstate coverage during training
Difference in EEG microstate time coverage (%) between training and rest periods for each session (session 2, session 3) independently.
Change in microstate coverage during rest
Difference in EEG microstate time coverage (%) between rest periods for each session (session 2, session 3) independently.

Secondary Outcome Measures

Correlations between EEG microstate time coverage (%) and task performance: error rates (%) and reaction time.
Change in EEG Event Related potentiels before and after neurofeedback training.
For each condition (Go/NoGo) we will investigate differences in Global map dissimilarity (GMD), amplitude and microstate segmentation between pre and post neurofeedback training tasks.

Full Information

First Posted
October 10, 2022
Last Updated
October 13, 2022
Sponsor
Nader Perroud
Collaborators
University of Geneva, Switzerland, University Hospital, Geneva
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1. Study Identification

Unique Protocol Identification Number
NCT05582928
Brief Title
Effects of EEG- Microstate Neurofeedback on Attention and Impulsivity in Adult Attention-deficit/Hyperactivity Disorder (ADHD) and Neurotypical Controls
Acronym
ADHDmicroNFB
Official Title
Effects of EEG- Microstate Neurofeedback on Attention and Impulsivity in Adult Attention-deficit/Hyperactivity Disorder (ADHD) and Neurotypical Controls
Study Type
Interventional

2. Study Status

Record Verification Date
October 2022
Overall Recruitment Status
Recruiting
Study Start Date
September 19, 2022 (Actual)
Primary Completion Date
June 2025 (Anticipated)
Study Completion Date
June 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Nader Perroud
Collaborators
University of Geneva, Switzerland, University Hospital, Geneva

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
EEG neurofeedback (NFB) may represent a new therapeutic opportunity for ADHD, a neuropsychiatric disorder characterized by attentional deficits and high impulsivity. Recent research of the Geneva group has demonstrated the ability of ADHD patients to control specific features of their EEG (notably alpha desynchronization) and that this control was associated with reduced impulsivity. In addition, alterations in EEG brain microstates (i.e., recurrent stable periods of short duration) have been described in adult ADHD patients, potentially representing a biomarker of the disorder. The present study aims to use neurofeedback to manipulate EEG microstates in ADHD patients and healthy controls, in order to observe the effects on neurophysiological, clinical and behavioural parameters.
Detailed Description
Neurofeedback (NFB) is a broadly used method that enables individuals to self-regulate one or more neurophysiological parameters. In the case of electroencephalography (EEG) the parameters most often used so far are slow cortical potentials (SCPs), coherence training and frequency training. Protocols based on these measures have been applied to many clinical populations exhibiting abnormal EEG patterns including schizophrenia, insomnia, dyslexia, drug addiction, autistic spectrum disorder and attention deficit/hyperactivity disorder (ADHD). Today, the most widely used neurofeedback protocol for the ADHD population is based on the theta/beta ratio (TBR). However more recent studies have failed to replicate this finding of elevated TBR as a diagnostic feature in ADHD, which was also confirmed in a meta-analysis. These divergent results motivate the need for research to explore new markers to diagnose and treat ADHD. In a recent study, Férat and colleagues proposed EEG microstate analysis as a new framework to study ADHD. Microstate analysis models spontaneous EEG as a sequence of states defined by recurring appearance of a given distribution of scalp potentials. The authors observed a significantly increased contribution of one specific state commonly referred to microstate D in the ADHD population compared to healthy subjects. This state is often associated with attentional functions and brain regions in the dorsal attention networks are involved . It would therefore be interesting to study the causal link between this microstate and attention by manipulating this biomarker with neurofeedback. In this context, a recent study by Hernandez and colleagues has already demonstrated that healthy participants were able to control such brain microstates by neurofeedback. The aim of the present study is to test whether patients with ADHD are also capable of self-regulating their microstate dynamics. In the light of recent findings on EEG microstate and the ADHD population, the hypothesis is that microstate D could be a potential functional biomarker of ADHD. To test it, the proposal is to modulate this microstate using a neurofeedback training protocol directly targeting microstate parameters. According to the main hypothesis, changes in microstate parameters should be correlated with change in attentional and impulsive behaviour. To answer this question, a two-session study was designed, where participants will perform a continuous performance task (CPT) before and after 30 minutes of microstate-based neurofeedback training. During one of the sessions participants will be trained to upregulate microstate parameters, while during the other one, they will be trained to downregulate the same parameters. Intra- and across-section statistical contrasts, both in terms of brain activity changes and behavioural performance, should provide evidence to evaluate the impact of microstate changes relative to behaviour. In addition, and according to a large number of studies on ERP components in ADHD patients the recording of event related potentials (ERPs) during the behavioural task could help us understand the neurophysiological changes linked to attention and impulsivity measures.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
ADHD, Healthy

7. Study Design

Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
Participant
Allocation
Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
healthy population group
Arm Type
Experimental
Arm Description
The experimental design includes three sessions: session 1 will be used to evaluate diagnostic using different targeted questionnaires. sessions 2 and 3 will be decomposed into 3 consecutives parts: Pre evaluation Neurofeedback Post evaluation
Arm Title
ADHD population group
Arm Type
Experimental
Arm Description
The experimental design includes three sessions: session 1 will be used to evaluate diagnostic using different targeted questionnaires. sessions 2 and 3 will be decomposed into 3 consecutives parts: Pre evaluation Neurofeedback Post evaluation
Intervention Type
Device
Intervention Name(s)
Neurofeedback
Intervention Description
Neurofeedback training during which participant will be asked to change the size of a bar using different strategies to vary the parameters of its current brain's states (neurofeedback training) computed on the realtime EEG signals.
Primary Outcome Measure Information:
Title
Change in microstate coverage during training
Description
Difference in EEG microstate time coverage (%) between training and rest periods for each session (session 2, session 3) independently.
Time Frame
Change within session at week 1 (session 2) and week 2 (session 2)
Title
Change in microstate coverage during rest
Description
Difference in EEG microstate time coverage (%) between rest periods for each session (session 2, session 3) independently.
Time Frame
Change within session week 1 (session 2) and week 2 (session 2)
Secondary Outcome Measure Information:
Title
Correlations between EEG microstate time coverage (%) and task performance: error rates (%) and reaction time.
Time Frame
Within session at week 1 (session 2) and week 2 (session 2)
Title
Change in EEG Event Related potentiels before and after neurofeedback training.
Description
For each condition (Go/NoGo) we will investigate differences in Global map dissimilarity (GMD), amplitude and microstate segmentation between pre and post neurofeedback training tasks.
Time Frame
Within session at week 1 (session 2) and week 2 (session 2)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
ADHD POPULATION GROUP A subject will be eligible if all the following criteria apply: Age: between 18-50 years Gender: male and female Health: general good health and normal or corrected-to-normal visual acuity Patients clinically able to stop the following psychotropic medications for 48h: psychostimulants, benzodiazepines Having provided written informed written consent A subject will not be eligible if any of the following criteria apply: Past or current history of a clinically significant central nervous system disorder, including structural brain abnormalities; cerebrovascular disease; history of other neurological disease, epilepsy, stroke or head trauma (defined as loss of consciousness > 5 min or requiring hospitalization) Impaired vision (normal or corrected acuity below 20/40) Medical illness (e.g., cardiovascular disease, renal failure, hepatic dysfunction) Comorbidities with current psychiatric disorders (bipolar disorder, borderline personality disorder, major depressive disorder, anxiety disorder) including substance use disorder as defined by the DIGS. HEALTHY POPULATION GROUP A subject will be eligible if all of the following criteria apply: Age: between 18-50 years Gender: male and female Health: general good health and normal or corrected-to-normal visual acuity Having provided written informed written consent A subject will not be eligible if any of the following criteria apply: Past or current history of ADHD Past or current history of main psychiatric disorders (bipolar disorder, borderline personality disorder, major depressive disorder, anxiety disorder), including substance use disorder as defined by the DIGS. Past or current history of a clinically significant central nervous system disorder, including structural brain abnormalities; cerebrovascular disease; history of other neurological disease, including epilepsy, stroke or head trauma (defined as loss of consciousness > 5 min or requiring hospitalization) Impaired vision (normal or corrected acuity below 20/40) Medical illness (e.g., cardiovascular disease, renal failure, hepatic dysfunction)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Nader Perroud, Professor
Phone
+41 22 305 45 11
Email
nader.perroud@hcuge.ch
First Name & Middle Initial & Last Name or Official Title & Degree
Marie-Pierre Deiber, PhD
Phone
+41 22 379 11 25
Email
marie-pierre.deiber@hcuge.ch
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Nader Perroud, Professor
Organizational Affiliation
University Hospital, Geneva
Official's Role
Principal Investigator
Facility Information:
Facility Name
TRE Unit (Trouble de la Régulation Emotionnelle) Department of psychiatry, HUG
City
Geneva
ZIP/Postal Code
1201
Country
Switzerland
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Nader Perroud, Professor
Phone
+41 (0)22 305 45 11
Email
nader.perroud@hcuge.ch
First Name & Middle Initial & Last Name & Degree
Roland Hasler, PhD
Phone
+41 (0)22 305 45 11
Email
roland.hasler@hcuge.ch

12. IPD Sharing Statement

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Effects of EEG- Microstate Neurofeedback on Attention and Impulsivity in Adult Attention-deficit/Hyperactivity Disorder (ADHD) and Neurotypical Controls

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