- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03297437
Predictors for Successful Neurofeedback Training (Predictors)
September 28, 2017 updated by: Frank Scharnowski
The primary objective of this study is to identify predictors of neurofeedback training success.
Study Overview
Detailed Description
In the last decades, neurofeedback has been established as a promising scientific tool.
Learning voluntary control over their own brain activity allows for establishing causal links between brain activity and mental functions.
However, patients participants differ in their ability to learn control over their own brain activity with neurofeedback.
It is thus crucial to understand why some participants are more successful in regulating their own brain activity than others.
The objective of the present study is thus to identify predictors for successful learning self-regulation with real-time fMRI neurofeedback.
To achieve this goal, we will evaluate the introspection ability of healthy participants using standardized psychological questionnaires and tasks.
These scores will then be correlated with how well they learned self-regulation skills using established real-time fMRI neurofeedback protocols.
Study Type
Interventional
Enrollment (Anticipated)
192
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Frank Scharnowski, Prof. Dr.
- Phone Number: +41443842953
- Email: Frank.Scharnowski@uzh.ch
Study Locations
-
-
Zürich-
-
Zürich, Zürich-, Switzerland, 8032
- Recruiting
- Hospital of Psychiatry, University of Zurich
-
Contact:
- Frank Scharnowski, Prof. Dr.
- Phone Number: +41443842953
- Email: Frank.Scharnowski@uzh.ch
-
Contact:
- Ronald Sladky, PD Dr.
- Phone Number: +41443842667
- Email: ronald.sladky@uzh.ch
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 65 years (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
Age 18 - 65 years. Magnetic resonance imaging compatibility.
Exclusion Criteria:
Physical or psychiatric disorders (DSM-V diagnosis). Current substance abuse. Exclusion criteria applicable to MRI (metallic implants, claustrophobia, epilepsy).
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Randomized
- Interventional Model: Single Group Assignment
- Masking: Triple
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
correlation between introspection scores and learning success
Time Frame: 48 months
|
The primary outcome measure is a correlation between introspection scores and neurofeedback learning success across all subjects.
|
48 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Anticipated)
October 1, 2017
Primary Completion (Anticipated)
September 30, 2021
Study Completion (Anticipated)
September 30, 2021
Study Registration Dates
First Submitted
September 26, 2017
First Submitted That Met QC Criteria
September 26, 2017
First Posted (Actual)
September 29, 2017
Study Record Updates
Last Update Posted (Actual)
October 2, 2017
Last Update Submitted That Met QC Criteria
September 28, 2017
Last Verified
September 1, 2017
More Information
Terms related to this study
Other Study ID Numbers
- PsychiatricUHZPUK
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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