Status:

COMPLETED

A Neurocognitive Model of Anorexia Nervosa

Lead Sponsor:

New York State Psychiatric Institute

Collaborating Sponsors:

Klarman Family Foundation

National Institute of Mental Health (NIMH)

Conditions:

Anorexia Nervosa

Eligibility:

All Genders

16-45 years

Brief Summary

The purpose of this study is to investigate thought processes and neural mechanisms that may contribute to the development of habitual behaviors. The investigators hypothesize that patients with AN wi...

Detailed Description

Patients with Anorexia Nervosa (AN) have extreme difficulty changing their eating behavior, even when they express desire for change. These behaviors seem to override all other potential responses, an...

Eligibility Criteria

Inclusion

  • Inclusion:
  • DSM-IV-TR™ diagnosis of anorexia nervosa (restricting or binge-purge subtype), current or prior;
  • Age 16-45;
  • Inpatient on GCRU
  • Medically stable.
  • Exclusion:
  • Any other current major Axis I disorder (including current bulimia nervosa), except major depression;
  • History of concussion, seizure disorder, or other neurological illness;
  • History of learning disability;
  • Acute Suicidality
  • Healthy comparison group:
  • Inclusion:
  • No current or past psychiatric illness;
  • Age 16-45
  • No history of binge eating or vomiting;
  • Normal weight (80%-120% ideal body weight)
  • Exclusion:
  • Significant medical or neurologic illness(concussion, seizure disorder, learning disability, other neurological illness)
  • Current psychotropic medication or medications known to impact cognition
  • Additional Exclusion Criteria for fMRI:
  • Significant Claustrophobia
  • Pregnancy
  • Indwelling metallic object, non-removable metal jewelry, medicinal patch or recent metallic ink tattoo
  • For patients, current psychotropic medications (antidepressants for 2 week (prozac and antipsychotics for 4 weeks)
  • For patients, any other current Axis I diagnosis

Exclusion

    Key Trial Info

    Start Date :

    May 1 2006

    Trial Type :

    OBSERVATIONAL

    Allocation :

    ACTUAL

    End Date :

    May 1 2014

    Estimated Enrollment :

    152 Patients enrolled

    Trial Details

    Trial ID

    NCT00325520

    Start Date

    May 1 2006

    End Date

    May 1 2014

    Last Update

    August 15 2014

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