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fMRI in Blood Phobia Syncope

This study has been withdrawn prior to enrollment.
(Could not get funding for fMRI studies at this time.)
National Institutes of Health (NIH)
Information provided by (Responsible Party):
Satish R. Raj, Vanderbilt University Identifier:
First received: July 10, 2008
Last updated: January 7, 2013
Last verified: January 2013
We plan to study patient who faint in response to the sight of blood and compare them to healthy subjects who do not. We are going to use a special type of MRI scan (functional MRI) to determine if there are differences in brain activation in response to seeing bloody or gory pictures that occur before the fainting occurs.

Condition Intervention
Blood Injury Phobia
Autonomic Dysfunction
Procedure: fMRI Scan

Study Type: Observational
Study Design: Observational Model: Case Control
Time Perspective: Prospective
Official Title: Neuroimaging in Blood Phobia Syncope

Resource links provided by NLM:

Further study details as provided by Satish R. Raj, Vanderbilt University:

Primary Outcome Measures:
  • fMRI BOLD signal [ Time Frame: Immediate ]

Secondary Outcome Measures:
  • Blood Injection Symptoms Scale [ Time Frame: Single visit ]
  • Disgust Scale (Revised) [ Time Frame: Single Visit ]

Enrollment: 0
Study Start Date: June 2010
Estimated Study Completion Date: June 2010
Estimated Primary Completion Date: June 2010 (Final data collection date for primary outcome measure)
Groups/Cohorts Assigned Interventions
Healthy control subjects (who do not faint at the sight of blood)
Procedure: fMRI Scan
Subjects will undergo a functional MRI scan of the head lasting ~45 minutes. They will be repeatedly shown video clips of blood, other disgusting things, or are neutral.
People who faint at sight of blood
Procedure: fMRI Scan
Subjects will undergo a functional MRI scan of the head lasting ~45 minutes. They will be repeatedly shown video clips of blood, other disgusting things, or are neutral.

Detailed Description:
Another aim of the study is to determine whether or not differences in personality traits among people with blood phobia is associated with differences in BOLD signal responses during fMRI.

Ages Eligible for Study:   18 Years to 30 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population
  1. Patients with at least 1 prior syncopal episode in response to viewing blood
  2. Healthy subjects without a history of syncope

Inclusion Criteria:

  • 18-30 years of age
  • 1. History of at least one syncopal episode upon exposure to viewing blood (Case Group)
  • Negative urine pregnancy test on study day

Exclusion Criteria:

  • Vasoactive medications (within 2 weeks of study day)
  • antihypertensives
  • beta blockers
  • vasoconstrictors
  • Psychotropic medications (within 4 weeks of study day)
  • History of psychostimulant or opiate use
  • History of alcohol, benzodiazepine or cannabis abuse or dependence
  Contacts and Locations
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Please refer to this study by its identifier: NCT00715065

United States, Tennessee
Vanderbilt University Autonomic Dysfunction Center
Nashville, Tennessee, United States, 37232-2195
Sponsors and Collaborators
Vanderbilt University
National Institutes of Health (NIH)
Principal Investigator: Satish R Raj, MD MSCI Vanderbilt University
  More Information

Responsible Party: Satish R. Raj, Assistant Professor, Vanderbilt University Identifier: NCT00715065     History of Changes
Other Study ID Numbers: 080608
NIH UL1 RR024975
Study First Received: July 10, 2008
Last Updated: January 7, 2013

Keywords provided by Satish R. Raj, Vanderbilt University:
blood injury phobia

Additional relevant MeSH terms:
Phobic Disorders
Autonomic Nervous System Diseases
Primary Dysautonomias
Consciousness Disorders
Neurobehavioral Manifestations
Neurologic Manifestations
Nervous System Diseases
Signs and Symptoms
Anxiety Disorders
Mental Disorders processed this record on May 25, 2017