Phase
Condition
N/ATreatment
Ventral tegmental area of dopaminergic midbrain (VTA) fMRI neurofeedback
Clinical Study ID
Ages 18-45 All Genders Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Age between 18 and 45 years
Male or female
Right-handed
In good general health
Women of childbearing capacity: use of effective method of birth control
Exclusion
Exclusion Criteria:
Current or diagnosis within past six months of an DSM-V Axis I or Axis II disorder (self-reported)
CES-D score of 20 or higher (indicating significant current depression symptoms)
Current or past six month use of prescription medications indicated for psychiatricconditions (e.g.,depression, anxiety)
Current serious medical illness (self-reported)
Head injury resulting in loss of consciousness
For participants age > 59 years, a total scaled score < 8 on the Dementia RatingScale-2.
A clinically-defined neurological disorder including, but not limited to:
Any condition likely to be associated with increased intracranial pressure
Space occupying brain lesion
History of stroke
Transient ischemic attack within two years
Cerebral aneurysm
Dementia
Mini Mental Status Exam (MMSE) score of <24
Parkinson's disease
Huntington's disease
Multiple sclerosis
Presence of cochlear implants or other implanted electronic devices or non-removablemetal (e.g., non-removable piercing, IUD)
History of an eye injury involving metal. Participants who worked with metal may beallowed to participate on a case-by-case basis with prior written approval fromBIAC.
Claustrophobia or unwillingness to tolerate the confinement associated with being inthe MRI scanner.
Weight of more than 250 pounds
Study Design
Study Description
Connect with a study center
Center for Cognitive Neuroscience
Durham, North Carolina 27708
United StatesActive - Recruiting
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