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Completed

NCT Number: NCT00205933

Behavioral Processes Underlying Reward Processing in Depression

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

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Key information

Age range

18 year–64 year

Sex eligibility

All sexes

Study type

Observational

Primary location

The Depression Clinical and Research Program, Massachusetts General Hospital, Boston, Massachusetts, United States

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About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Sponsors and collaborators

Lead sponsor

Affective Neuroscience Laboratory

Other

Collaborators

  • Massachusetts General Hospital

Registry information

Important dates

Study start
2004
Study completion
2007
First posted
Sep 21, 2005
Registry last updated
Dec 6, 2007

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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