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Food Exposure Therapy in Anorexia Nervosa

Food Exposure Therapy in Anorexia Nervosa

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00755820
Enrollment
32
Registered
2008-09-19
Start date
2008-01-31
Completion date
2012-01-31
Last updated
2012-10-26

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

Conditions

Anorexia Nervosa

Brief summary

This is a research study to determine whether a medication called D-cycloserine (DCS) in combination with a type of psychotherapy called Exposure Therapy is helpful to patients with anorexia nervosa.

Detailed description

This is a research study to determine whether a medication called D-cycloserine (DCS) in combination with a type of psychotherapy called Exposure Therapy is helpful to patients with anorexia nervosa. DCS is approved by the FDA as an antibiotic medication, but has not been approved by the FDA for the treatment of anorexia nervosa. Past studies have found that DCS together with Exposure Therapy can help people with height phobia, social phobia, and obsessive compulsive disorder. Anorexia nervosa often includes phobia-like fears, obsessive thoughts, and compulsive rituals, so the current study aims to determine whether DCS paired with Exposure Therapy can also help people with anorexia nervosa. Anorexia nervosa is a disorder characterized by self-starvation, extreme weight loss, and difficulty maintaining a normal weight. You have been asked to participate in this study because you have been given a diagnosis of anorexia nervosa. In this study you will receive one of three therapies: Exposure Therapy with DCS, Exposure Therapy with placebo (inactive medication), or Treatment as Usual. You will participate in a total of four test meals in a laboratory setting. A total of 70 individuals with anorexia nervosa will participate in this study. Twenty individuals who have never had an eating disorder will participate in one portion of this study.

Interventions

BEHAVIORALExposure Therapy + D-Cycloserine

Exposure therapy with d-cycloserine medication

BEHAVIORALExposure Therapy + Placebo

Exposure therapy with placebo medication

BEHAVIORALSupportive Psychotherapy

Supportive psychotherapy

Sponsors

The Hilda & Preston Davis Foundation
CollaboratorOTHER
National Alliance for Research on Schizophrenia and Depression
CollaboratorOTHER
New York State Psychiatric Institute
Lead SponsorOTHER

Study design

Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

for Patients: * DSM-IV-TR™ diagnosis of anorexia nervosa (restricting or binge-purge subtype) on admission * Subjects will have achieved 90% of ideal body weight (IBW) * Age 18-45 * Medically stable * Participation in inpatient treatment * Subjects must have signed informed consent document indicating that they understand the purpose of and procedures required for the study and are willing to participate in the study.

Exclusion criteria

for Patients: * Any other current major Axis I disorder, except OCD or MDD (mild) * On psychotropic medication, including benzodiazepines (At the start of the study, subjects will be free of fluoxetine for 4 weeks, and free of all other medications for a minimum of 2 weeks.) * History of a seizure disorder * Abnormal liver function * Renal insufficiency * Known hypersensitivity to D-cycloserine * Pregnant or lactating * Acute suicidality (suicidality or self injury in the last 3 months) Inclusion Criteria for Healthy Controls: * BMI ≥ 19.0 kg/m2 * Age 18-45 years * Subjects must have signed informed consent document indicating that they understand the purpose of and procedures required for the study and are willing to participate in the study.

Countries

United States

Outcome results

None listed

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