Eligibility Module

Eligibility Module

The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.

Eligibility Module path is as follows:

Study -> Protocol Section -> Eligibility Module

Eligibility Module


Ignite Creation Date: 2025-12-24 @ 9:33 PM
Ignite Modification Date: 2025-12-24 @ 9:33 PM
NCT ID: NCT01849432
Eligibility Criteria: Inclusion Criteria: * 18 - 65 years of age * Right-handed (Edinburgh Inventory - Oldfield 1971) * SCID diagnosis consistent with group designation: Current PTSD (PTSD group; none current or past (NC and TENC group); Current SP (must be to small animal phobia, SP group); Current PD (PD group) * To be matched for age, gender, and years of education, as well as self-identified race/ethnicity. * For female subjects, stage of menstrual cycle will be ascertained by history (see appendix), and dates of fMRI acquisition will be scheduled to prevent systematic differences between groups with respect to this variable. Exclusion Criteria: * Neurologic or medical condition that would interfere with study procedures or confound results, ascertained by history. * History of seizure or significant head trauma (i.e., extended loss of consciousness, neurological sequelae, or known structural brain lesion) * History of exclusionary Axis I psychiatric diagnosis (other than as specified); i.e., history of substance use disorder, psychotic disorder, bipolar disorder, tic disorder, or eating disorder. Note that comorbid current major depressive disorder will be allowed in up to one half of each study group. This will enable inclusion of this common comorbidity, but also enable a definitive assessment of whether or not the presence of this comorbid diagnosis is driving any observed significant between group differences. * Use of psychotropic medication within 4 weeks prior to study (within 6 weeks for fluoxetine, or other long-lived compounds; within one year for neuroleptics). * Pregnancy (to be ruled out by urine ß-HCG). * Metallic implants or devices contraindicating magnetic resonance imaging.
Healthy Volunteers: True
Sex: ALL
Minimum Age: 18 Years
Maximum Age: 65 Years
Study: NCT01849432
Study Brief:
Protocol Section: NCT01849432