このページは自動翻訳されたものであり、翻訳の正確性は保証されていません。を参照してください。 英語版 ソーステキスト用。

The Functional Anatomy of Personality Trait Knowledge: An fMRI Study

The Functional Anatomy of Personality Trait Knowledge: an fMRI Study

This study will identify the regions of the brain that are involved in personality trait knowledge-that is, what a person knows about aspects of personality such as "generous," "honest," and others. It will also examine brain areas relating to a person's knowledge of how likeable those personality traits are, being familiar with the traits, and the degree of associating such traits with one's self. There has not been any previous study, through modern imaging techniques, on the location of the brain and the concepts of personality traits.

Patients ages 21 to 65 who are in good health, are right handed, and native speakers of English may be eligible for this study. Pregnant women are not eligible. There will be 200 participants involved in pencil-and-paper or computer tasks. Also, there will be three functional magnetic resonance imaging (fMRI) experiments with 32 participants. Patients may participate in up to three fMRI experiments.

Patients will be recruited through NIH's Normal Control Database. They would need to have had a neuroexamination conducted by an NIH doctor within the last year. Patients will be interviewed for any medical, neurological, or psychological condition that would make it difficult to read the fMRI results. Depending on the studies that patients take part in, they will have different questionnaires to complete. They may also perform a computerized test that measures word associations. These tests will take about 1 to 2 hours.

The technique of MRI uses a strong magnetic field and radio waves to obtain images of body organs and tissues. During the initial MRI scan, patients will lie still on a table that will slide into the enclosed tunnel of the scanner. They will be in the scanner not longer than 2 hours. During the procedure, they may be asked to lie as still as possible for up to 1 hour at a time. As the scanner takes pictures, patients will hear knocking or beeping sounds, and they will wear earplugs to reduce the noise. Patients will be able to communicate with the MRI staff at all times during the scan, and they may ask to be moved out of the machine at any time. Then the functional MRI (fMRI) scan will involve taking pictures of the brain while patients are performing tasks. All the tasks will be explained, and patients will have the chance to practice them before entering the scanner. For this activity, patients will be asked to make decisions about what they are seeing in the tasks presented to them. They will decide "yes" and "no" by pressing a left or right button. This scan will take about 1 hour. Afterward, patients may be asked to fill out written questionnaires or to perform reaction time tasks by using a computer.

This study will not have a direct benefit for participants. However, it is hoped that information gained will enhance researchers' understanding about which areas of the brain are necessary to perform certain tasks.

調査の概要

状態

完了

条件

詳細な説明

Objective. The purpose of the protocol is to identify the brain regions involved in personality trait knowledge, associated affective valence and person-trait associations. We propose using parametric event-related fMRI in addition to classical reaction time measures, to answer the question of whether a specialized neural system is involved in semantic processing of personality trait concepts. We will apply methods that have been used in previous investigations to identify category-specific semantic (meaning) systems for living and non-living objects.

Study Population. Healthy, normal adult, right-handed volunteers will be studied during functional neuroimaging and in behavioral pre-tests.

Design. Behavioral pre-tests (N=200 subjects) are used to obtain psycholinguistic stimulus parameters used in the fMRI experiments. Three parametric event-related functional MRI experiments (for a total of 104 subjects) using personality trait concept words as main input stimuli will be conducted.

Outcome Measures. The data collected will consist of questionnaire results, behavioral measures of cognitive performance and corresponding fMRI images. The results gained from this protocol will be of value in advancing the neuroscience of person perception and social cognition.

研究の種類

観察的

入学 (実際)

190

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究場所

    • Maryland
      • Bethesda、Maryland、アメリカ、20892
        • National Institutes of Health Clinical Center, 9000 Rockville Pike

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

21年~65年 (大人、高齢者)

健康ボランティアの受け入れ

いいえ

受講資格のある性別

全て

説明

  • INCLUSION CRITERIA:

In all the studies, subjects will consist of healthy, native English-speaking, right-handed volunteers, as measured by the Edinburgh Handedness Inventory (Oldfield, 1971). Subjects will range in age from 21 to 65 years old and they will be included regardless of race and gender.

EXCLUSION CRITERIA:

Non-native English speakers and non-right handers will be excluded as mentioned above, as will non-neurologically normal volunteers. Subjects younger than 21 and older than 65 will be excluded. A urine pregnancy test will be employed with all women of childbearing age no more than 24 hours prior to the MRI. The results must be negative in order to proceed with the MRI.

Participants with any of the following: aneurysm clip; implanted neural stimulator; implanted cardiac pacemaker or auto-defibrillator; cochlear implant; ocular foreign body, e.g. metal shavings; permanent eyeliner; insulin pump; or irremovable body piercing will be excluded from the study due to the possible dangerous effects of the magnet upon metal objects in the body. Participants taking central nervous system active medications will be excluded.

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

出版物と役立つリンク

研究に関する情報を入力する責任者は、自発的にこれらの出版物を提供します。これらは、研究に関連するあらゆるものに関するものである可能性があります。

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始

2004年10月29日

研究の完了

2011年12月29日

試験登録日

最初に提出

2004年11月3日

QC基準を満たした最初の提出物

2004年11月3日

最初の投稿 (見積もり)

2004年11月4日

学習記録の更新

投稿された最後の更新 (実際)

2017年7月2日

QC基準を満たした最後の更新が送信されました

2017年6月30日

最終確認日

2011年12月29日

詳しくは

本研究に関する用語

その他の研究ID番号

  • 050018
  • 05-N-0018

この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。

3
購読する