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Affective Processing in Depression and Epilepsy

NCT00855725 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 14

Last updated 2009-07-09

No results posted yet for this study

Summary

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

Conditions

Interventions

OTHER

fMRI

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

OTHER

Hamilton Depression Rating Scale

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

OTHER

Beck's Depressive Inventory

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

OTHER

Interictal 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 & Collaborators

  • Northwell Health

    lead OTHER

Principal Investigators

  • Alan Ettinger, M.D. · Northwell Health

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2008-06-30
Primary Completion
2009-06-30
Completion
2009-06-30

Countries

  • United States

Study Locations

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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00855725 on ClinicalTrials.gov