Locating Regions of Interest in Generalized Anxiety Disorder Using Function Magnetic Resonance Imaging (fMRI)

NCT ID: NCT01607710

Last Updated: 2014-09-05

Basic Information

• Recruitment Status: COMPLETED
• Total Enrollment: 55 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2012-07-31
• Study Completion Date: 2014-06-30

Brief Summary

The investigators are seeking to locate the brain regions of interest in generalized anxiety disorder (GAD) using both structural (sMRI) and functional magnetic resonance imaging (fMRI). The MRI will be used to measure changes in blood flow in the brain while at rest and while completing tasks designed to elicit symptoms of anxiety. Results from a nonclinical control group and a GAD group will be compared to determine whether they exhibit different areas of brain activity during the tasks.

Detailed Description

20 healthy controls and 20 participants with GAD will be recruited. Each participant will undergo an MRI session that will last approximately 2 hours. The structural MRI will be used when the participant is at rest. During the functional MRI (fMRI), a computer screen inside the scanner will display four tasks the participant must complete: (1)Gambling Task, (2)Risk & Ambiguity Task, (3)Reading Emotion from the Eyes (REE) Task, and (4)Emotional Counting Task.

Conditions

Generalized Anxiety Disorder

Study Design

• Observational Model Type: CASE_CONTROL
• Study Time Perspective: CROSS_SECTIONAL

Study Groups

Generalized Anxiety Disorder

The group of participants diagnosed with generalized anxiety disorder.

No interventions assigned to this group

Nonclinical Control Group

The comparison group of participants with no psychiatric diagnoses.

No interventions assigned to this group

Eligibility Criteria

Inclusion Criteria

• Clinical diagnosis of Generalized Anxiety Disorder
• Hamilton Anxiety Rating Scale score of 18 or higher
• Hamilton Rating Scale for Depression score of 17 or less
• Fluency in English
• Capacity to understand the nature of the study and willingness to sign informed consent for

• Absence of any psychiatric diagnosis

Exclusion Criteria

• History of epilepsy or head trauma (Loss of consciousness>5 minutes) with the past 6 months
• Lifetime history of increased intracranial pressure, seizure disorder, stroke, brain tumor, multiple sclerosis or brain surgery
• A review of patient medications by the study physician indicates an increased risk of seizure
• An active autoimmune, endocrine, viral, or vascular disorder affecting the brain; any unstable cardiac disease; hypertension; or severe renal or liver insufficiency
• Substance use disorder or posttraumatic stress disorder (PTSD) within the past 6 months
• Lifetime bipolar disorder, obsessive-compulsive disorder (OCD), psychotic disorder, mental retardation, or pervasive development disorder
• Any psychotic features, including dementia or delirium
• Medication change within past 3 months
• Current serious suicidal or homicidal ideation, and/or serious suicidal attempt within past 6 months
• Serious, unstable, or terminal medical condition or clinically judged too psychiatrically unstable to participate in the study
• Any contraindication for participation in MRI scan

Nonclinical Control Group:

• History of epilepsy or head trauma (Loss of Consciousness>5 minutes) with the past 6 months
• Lifetime history of increased intracranial pressure, seizure disorder, stroke, brain tumor, multiple sclerosis or brain surgery
• A review of patient medications by the study physician indicates an increased risk of seizure
• An active autoimmune, endocrine, viral, or vascular disorder affecting the brain; any unstable cardiac disease; hypertension; or severe renal or liver insufficiency
• Substance use disorder or PTSD within the past 6 months
• Lifetime bipolar disorder, OCD, psychotic disorder, mental retardation, or pervasive development disorder
• Any psychotic features, including dementia or delirium
• Medication change within past 3 months
• Current serious suicidal or homicidal ideation, and/or serious suicidal attempt within past 6 months
• Serious, unstable, or terminal medical condition or clinically judged too psychiatrically unstable to participate in the study
• Any contraindication for participation in MRI scan

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Hartford Hospital

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Gretchen J Diefenbach, Ph.D.

Role: PRINCIPAL_INVESTIGATOR

Hartford Hospital

Locations

Hartford Hospital

Hartford, Connecticut, United States

Countries

United States

Other Identifiers

DIEF003523.2

Identifier Type: -

Identifier Source: org_study_id