Emotion Study -- A Neurofeedback Approach

NCT ID: NCT02194907

Last Updated: 2020-01-22

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

19 participants

Study Classification

INTERVENTIONAL

Study Start Date

2014-10-31

Study Completion Date

2020-01-08

Brief Summary

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This study will determine whether brain activity can be modified and improves performance on a task by showing participants live 'video feed' of their brains on advanced imaging technology. The study is particularly interested in brain regions that have been shown to be relevant for emotions, specifically the anterior insula and the medial prefrontal cortex. Advanced technology will map the brain using magnetic pulses with a real-time functional Magnetic Resonance Imaging (rt-fMRI) machine.

Detailed Description

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Overview: All participants of both age groups will be randomly divided (like tossing a coin) into two groups:

* One group will have training sessions using a special feedback technique to learn to actively increase blood flow in the front of the brain, while thinking of and viewing emotional faces, scenes, and text
* The other group will have training sessions using a special feedback technique to learn to actively increase blood flow in the back of the brain while thinking of and viewing emotional faces, scenes, and text

Further, each of these two groups will be divided into two sub-groups that are different with respect to the training procedure that is used:

\* Use of a 3.0 Tesla, 32-channel Seimens whole-body human MR scanner (fMRI) during training, that has not been associated with any known side effects or safety risks

Number of Study Visits:

This study has the following parts: A pre-training visit, six training visits, and a post-training visit.

With a few exceptions as explained below, the procedures during pre-training, training, and post-training visits are identical.

* At the beginning of the first visit, the investigator will tell the participant about the study and what is involved and will ask them to sign a consent form. The participant may ask as many questions as they would like before deciding about study participation.
* For each of the visits, the investigator will review questions with the participant about their health to ensure their eligibility to undergo fMRI on the day of testing.
* Also for each visit, the investigator will ask the participant to respond to a short questionnaire related to their current mood.
* In the pre-training and the post-training visits only, the investigator will ask the participant to answer questions about their feelings, emotions, and thoughts.
* For each of the participant's visits, they will spend 50-60 minutes either in the MRI scanner, while viewing pictures and text on a screen. During this time, pictures of the participant's brain at work and at rest will be acquired. In the training visits only, the participant will learn to increase blood flow in certain brain regions with the help of information presented to them on the screen.
* For each of the participant's visits, they will be asked to respond to a short questionnaire related to their current mood.
* In the pre-training/post-training visits only, the investigator will ask the participant to answer questions about their feelings, emotions, and thoughts as well as their personality. The participant will also perform brief tests related to the thinking process.
* At the end of each visit, the participant will complete a questionnaire about how they approached the study tasks and whether they experienced any discomfort in the MRI scanner or while wearing the fNIRS system.
* Upon study completion, the investigator will tell the participant about the general goals of the study and answer any questions that they may have.

The procedure can be stopped at any time.

The study will conclude with debriefing and reimbursement.

Conditions

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Aging Emotion

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

BASIC_SCIENCE

Blinding Strategy

NONE

Study Groups

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Anterior insula cortex activation

Participants will receive training sessions using a special feedback technique to learn to actively increase blood flow in the front of the brain, while thinking of and viewing emotional faces, scenes, and text.

Group Type ACTIVE_COMPARATOR

Brain activity training - anterior insula

Intervention Type BEHAVIORAL

training sessions using a special feedback technique to learn to actively increase blood flow in the front of the brain

Primary auditory cortex activation

Participants will have training sessions using a special feedback technique to learn to actively increase blood flow in the back of the brain while thinking of and viewing emotional faces, scenes, and text.

Group Type ACTIVE_COMPARATOR

Brain activity training - medial prefrontal cortex

Intervention Type BEHAVIORAL

training sessions using a special feedback technique to learn to actively increase blood flow in the back of the brain

Interventions

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Brain activity training - anterior insula

training sessions using a special feedback technique to learn to actively increase blood flow in the front of the brain

Intervention Type BEHAVIORAL

Brain activity training - medial prefrontal cortex

training sessions using a special feedback technique to learn to actively increase blood flow in the back of the brain

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* Between the ages of 18-30 years or 63-90 years
* Right-handed
* Native English speaker

Exclusion Criteria

* Pregnant or possibly pregnant
* Claustrophobia
* Large pieces of metal in the body, particularly in the face and neck.
* Piercings or metal implants that cannot be removed from the body
* Surgery on the brain or any prior serious brain damage or disease
* Dementia or severe cognitive disorders
Minimum Eligible Age

18 Years

Maximum Eligible Age

90 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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University of Florida

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Natalie Ebner, PhD

Role: PRINCIPAL_INVESTIGATOR

University of Florida, Department of Psychology

Locations

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University of Florida

Gainesville, Florida, United States

Site Status

Countries

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United States

Related Links

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http://www.frontiersin.org/articles/10.3389/fnagi.2016.00239/full

Real-Time fMRI in Neuroscience Research and Its Use in Studying the Aging Brain

Other Identifiers

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IRB201300814 closed

Identifier Type: -

Identifier Source: org_study_id

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