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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.

Studieoversikt

Status

Fullført

Forhold

Detaljert beskrivelse

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.

Studietype

Observasjonsmessig

Registrering

80

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiesteder

    • Maryland
      • Bethesda, Maryland, Forente stater, 20892
        • National Institute of Mental Health (NIMH)

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

  • Barn
  • Voksen
  • Eldre voksen

Tar imot friske frivillige

Ja

Kjønn som er kvalifisert for studier

Alle

Beskrivelse

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.

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Publikasjoner og nyttige lenker

Den som er ansvarlig for å legge inn informasjon om studien leverer frivillig disse publikasjonene. Disse kan handle om alt relatert til studiet.

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart

1. oktober 1998

Studiet fullført

1. oktober 2003

Datoer for studieregistrering

Først innsendt

3. november 1999

Først innsendt som oppfylte QC-kriteriene

3. november 1999

Først lagt ut (Anslag)

4. november 1999

Oppdateringer av studieposter

Sist oppdatering lagt ut (Anslag)

4. mars 2008

Siste oppdatering sendt inn som oppfylte QC-kriteriene

3. mars 2008

Sist bekreftet

1. oktober 2003

Mer informasjon

Begreper knyttet til denne studien

Andre studie-ID-numre

  • 990008
  • 99-M-0008

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .

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