The Impact of Familiarity and Emotional Attachment on the Visual Processing of Faces

This study uses functional magnetic resonance imaging (fMRI) to look at brain activity while patients view pictures of people's faces that they are familiar with or have emotional attachment to.

The functional MRI (fMRI) procedure allows researchers to "see the brain at work." It uses the same powerful magnetic fields and weak electromagnetic radiation (radiowaves) as standard structural MRI. However, functional MRI can also show areas of increased blood flow, which relates to increased activity by brain cells.

This research study builds on previous studies that identified specific areas of the brain that are activated by visual stimuli showing faces. However, previous research used anonymous faces as stimuli. This study will use faces of individuals known to the patient.

There are three experiments that will be conducted in the study;

  1. Experiment 1 will attempt to determine the effects of familiarity of the photographed face on brain activity patterns. Patients will view familiar faces, the faces of close friends and relatives, and the faces of famous people.
  2. Experiment 2 will look at how maternal attachment affects the response to visual stimuli. Mothers will view pictures of their first born child, as well as those of familiar children to whom they are not related, unfamiliar children, and unfamiliar adults.
  3. Experiment 3 will explore the effects of interpersonal attachment and loss on response to visual stimuli. In this experiment, bereaved spouses will view pictures of their deceased spouse, those of living family members, and those of unfamiliar people.

Study Overview

Status

Completed

Conditions

Detailed Description

This functional magnetic resonance imaging protocol uses a face recognition activation task to ascertain how brain activation patterns differ depending on the subject's familiarity with, and emotional attachment to, the person depicted in the visual stimulus. In a series of studies, subjects will view unfamiliar and familiar (including personally familiar and famous) faces; mothers will view pictures of their own child and those of familiar and unfamiliar children; and bereaved and non-bereaved spouses will view pictures of their spouse, other family members, and unfamiliar people. The use of emotionally significant faces as activation stimuli may help to elucidate the neural circuitry underlying interpersonal attachment and psychological responses to loss.

Study Type

Observational

Enrollment

80

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Maryland
      • Bethesda, Maryland, United States, 20892
        • National Institute of Mental Health (NIMH)

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

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

INCLUSION CRITERIA:

Subjects will be recruited through advertisements within Bethesda and surrounding communities.

All subjects must be right-handed.

For experiments #1 and 2, subjects will be 20-40 years old.

For study #3, subjects will be 45-75 years old.

For experiment #2, all subjects will be mothers with a non-adopted child aged 6-12 years old.

For experiment #3, subjects in the bereaved group will have become spousally bereaved within the past 6 months.

EXCLUSION CRITERIA:

Subjects will be excluded if they have a history of significant medical disorders (including learning disabilities, seizures, history of head trauma, hypertension, or cerebrovascular disease) or psychiatric disorders, including substance abuse. (An exception to this is that bereaved subjects in experiment #3 will not be excluded if they meet DSM-IV criteria for major depressive disorder (non-psychotic), adjustment disorder with depressed mood, or bereavement, as long as their current Hamilton-D score is less than 13).

Subjects will also be excluded if they take any prescribed medications (including birth control pills), if they are pregnant, or if their vision is inadequate to see the visual stimulus.

In addition, subjects in experiment #2 will receive a DICA-P (Diagnostic Interview for Children and Adolescents, Parent Version), and will be excluded if their child meets diagnostic criteria for a psychiatric illness.

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?

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

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

October 1, 1998

Study Completion

October 1, 2003

Study Registration Dates

First Submitted

November 3, 1999

First Submitted That Met QC Criteria

November 3, 1999

First Posted (Estimate)

November 4, 1999

Study Record Updates

Last Update Posted (Estimate)

March 4, 2008

Last Update Submitted That Met QC Criteria

March 3, 2008

Last Verified

October 1, 2003

More Information

Terms related to this study

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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