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Affective Processing in Depression and Epilepsy

Affective Processing in Depression and Epilepsy; An fMRI Study

Status
Terminated
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00855725
Enrollment
14
Registered
2009-03-04
Start date
2008-06-30
Completion date
2009-06-30
Last updated
2009-07-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Depression, Epilepsy, Healthy

Keywords

Epilepsy, Depression, Neurology, fMRI, Healthy Controls

Brief summary

The goal of this study is to determine whether there are unique markers on neuroimaging that are associated with depression in epilepsy.

Detailed description

Symptoms of depression is commonly seen in patients with epilepsy. There are similarities and differences between depressive symptoms in epilepsy when compared with primary depression. Through the use of fMRI (Functional MRI), we hope to determine whether there are unique markers on neuroimaging that are associated with depression in epilepsy.

Interventions

OTHERfMRI

Subjects will undergo MRI scanning to gather data about cognetive functions.

Investigator will evalute the subject during a one on one interview for depression using the Hamilton Depression Rating Scale.

OTHERBeck's Depressive Inventory

Subjects will complete self assessment to evaluate their level of depression.

OTHERInterictal Dysphoric Disorder Inventory (IDDI)

Subject will complete self assessment to determine if there have been any changes in mood, emotions and or feelings from time to time.

Sponsors

Northwell Health
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

For Control Group Inclusion Criteria: * Healthy adults of 18 years of age or older.

Exclusion criteria

* Subject has no history of affective disorders * Subject scores higher than 5 on Hamilton Depression Rating Scale * Subject with prior primary diagnosis of any psychotic disorder, bipolar disorder, anxiety disorder, or any other serious medical or neurological disorder * Subject is pregnant * Subject is unable to undergo a MRI Epilepsy Only Group Inclusion Criteria: * Subject is at least 18 years of age * Subject has confirmed temporal lobe epilepsy (TLE)

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026