Behavioral Processes Underlying Reward Processing in Depression

Sponsor
Affective Neuroscience Laboratory (Other)
Overall Status
Completed
CT.gov ID
NCT00205933
Collaborator
Massachusetts General Hospital (Other)
78
2
38
39
1

Study Details

Study Description

Brief Summary

The purpose of this project is to use behavioral techniques to investigate emotional processing in subjects with major depression and healthy comparison subjects.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    A promising strategy for parsing the heterogeneity of Major Depressive Disorder is to identify phenotypes characterized by reliable functional abnormalities. Anhedonia, the lack of reactivity to pleasurable stimuli, is considered a trait marker for depression. Using an objective behavioral task this project aims to investigate hedonic capacity in subjects meeting a DSM-IV diagnosis of Major Depressive Disorder.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    78 participants
    Observational Model:
    Cohort
    Time Perspective:
    Cross-Sectional
    Official Title:
    Behavioral Processes Underlying Reward Processing in Depression
    Study Start Date :
    Apr 1, 2004
    Actual Study Completion Date :
    Jun 1, 2007

    Outcome Measures

    Primary Outcome Measures

      Eligibility Criteria

      Criteria

      Ages Eligible for Study:
      18 Years to 64 Years
      Sexes Eligible for Study:
      All
      Accepts Healthy Volunteers:
      Yes
      Inclusion Criteria:
      Depressed participants:
      • Right-handed

      • DSM-IV diagnosis of MDD

      • Score of at least 17 on the 21-item HAM-D scale

      • Absence of any psychotropic medications for at least 2 weeks (6 months for dopaminergic drugs (including methylphenidate), 6 weeks for fluoxetine, and 4 weeks for neuroleptics and benzodiazepines because of longer half-lives.)

      • No current or past history of MDD with psychotic features

      • Absence of any other Axis I or Axis II diagnosis (Including bipolar disorder and current or lifetime history of alcohol or substance abuse or dependence.) Particularly, subjects with a history of alcoholism and substance abuse will be excluded, since dopaminergic alterations have been reported in these conditions. Exclusion of patients with comorbid Axis I or Axis II diagnoses will be necessary as evidence exists of alteration in dopamine receptor density in detached personality and social phobia. The alteration of dopamine in the brain may in turn alter behavior.

      • Absence of significant medical conditions

      • Absence of ECT in the previous 6 months

      • Ability to provide informed consent/authorization

      Bipolar participants:
      • Both genders and all ethnic origins

      • Age between 18 and 64

      • Right-handed

      • DSM-IV diagnosis of Bipolar Disorder I or II

      • Score of at least 17 on the 21-item Hamilton Depression Rating Scale (HAM-D)

      • Absence of any psychotropic medications for at least 2 weeks (6 months for dopaminergic drugs (including methylphenidate), 6 weeks for fluoxetine, and 4 weeks for neuroleptics and benzodiazepines because of longer half-lives.)

      • No current or past history of MDD with psychotic features

      • Absence of any other Axis I or Axis II diagnosis (Including current or lifetime history of alcohol or substance abuse or dependence.) Particularly, subjects with a history of alcoholism and substance abuse will be excluded.

      • Absence of significant medical conditions

      • Absence of ECT in the previous 6 months

      • Ability to provide informed consent/authorization

      Control Participants:
      • Right-handed

      • Absence of medical, neurological, and psychiatric illness (including alcohol and substance abuse), as assessed by the SCID

      • Absence of any medications for at least 2 weeks

      • Informed consent/authorization

      Exclusion Criteria:
      • Left-handed/ambidextrous

      • Evidence of neurological illness

      • Current alcohol or substance abuse

      • Serious suicide or homicide risk

      Contacts and Locations

      Locations

      Site City State Country Postal Code
      1 The Depression Clinical and Research Program, Massachusetts General Hospital Boston Massachusetts United States 02114
      2 Affective Neuroscience Laboratory, Department of Psychology, Harvard University Cambridge Massachusetts United States 02138

      Sponsors and Collaborators

      • Affective Neuroscience Laboratory
      • Massachusetts General Hospital

      Investigators

      • Principal Investigator: Diego A Pizzagalli, PhD, Harvard University

      Study Documents (Full-Text)

      None provided.

      More Information

      Publications

      None provided.
      Responsible Party:
      , ,
      ClinicalTrials.gov Identifier:
      NCT00205933
      Other Study ID Numbers:
      • 2003-P-000994
      First Posted:
      Sep 21, 2005
      Last Update Posted:
      Dec 6, 2007
      Last Verified:
      Nov 1, 2007

      Study Results

      No Results Posted as of Dec 6, 2007