Effectiveness of High Intensity Inpatient Versus Stepped Intensity Treatment for Anorexia Nervosa
Primary Purpose
Eating Disorders
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Structured Behavioral Treatment
Sponsored by
About this trial
This is an interventional treatment trial for Eating Disorders focused on measuring Anorexia Nervosa
Eligibility Criteria
Inclusion Criteria:
- Diagnosis of anorexia nervosa, according to DSM-IV criteria
- Body mass index (BMI) less than 18.5 kg/m2
Exclusion Criteria:
- Presence of psychosis or the axis I disorders of schizophrenia, bipolar disorder, or active substance abuse or dependence requiring specialized treatment
- Requires specialized treatment that is for major depression or anxiety disorders and is inconsistent with study treatments
- Any major medical illness requiring immediate medical treatment or that would affect clinical treatment associated with the study
- Significant risk of suicide
Sites / Locations
- New York State Psychiatric Institute
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
Continued inpatient treatment
Sequenced treatment
Arm Description
Participants will undergo inpatient hospital treatment until they have gained enough weight to be discharged.
Participants will begin with inpatient treatment, transition to day patient treatment, and then transition to outpatient treatment.
Outcomes
Primary Outcome Measures
Weight
Secondary Outcome Measures
Eating behaviors
Psychopathology associated with eating behaviors
Utilization of health care services
Full Information
NCT ID
NCT00815815
First Posted
December 29, 2008
Last Updated
September 19, 2023
Sponsor
New York State Psychiatric Institute
Collaborators
National Institute of Mental Health (NIMH)
1. Study Identification
Unique Protocol Identification Number
NCT00815815
Brief Title
Effectiveness of High Intensity Inpatient Versus Stepped Intensity Treatment for Anorexia Nervosa
Official Title
Anorexia Nervosa: The Importance of Treatment Intensity
Study Type
Interventional
2. Study Status
Record Verification Date
August 2013
Overall Recruitment Status
Completed
Study Start Date
February 2004 (undefined)
Primary Completion Date
February 2008 (Actual)
Study Completion Date
February 2008 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
New York State Psychiatric Institute
Collaborators
National Institute of Mental Health (NIMH)
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
This study will examine the effectiveness of inpatient treatment for anorexia nervosa versus a sequenced treatment that transitions from higher intensity inpatient care to lower intensity outpatient care.
Detailed Description
Anorexia nervosa is an eating disorder in which a person does not eat enough to maintain a healthy body weight. This disorder can lead to starvation, which may, in turn, lead to heart failure or brain damage. Anorexia can also lead to a host of other health problems, including mild anemia, swollen joints, and brittle bones. Treatment for anorexia begins by attempting to bring the anorexic person to a healthy body weight, while also conducting therapy aimed at developing habits and ways of thinking that promote maintenance of a healthy weight. Traditionally, the first part of this treatment-restoring healthy body weight-has taken place in inpatient hospital care. Recently, however, some patients have begun with high intensity inpatient care and then shifted to lower intensity outpatient care over the course of treatment. This study will compare the effectiveness of these two different methods of delivering treatment.
Length of participation in this study will vary, depending on the effectiveness of treatment. All participants will have follow-up assessments for 18 months after study entry. Every participant who passes the screening examination will be admitted to inpatient care in the study hospital. On Day 3 of their stay, participants will be randomly assigned to receive either continued inpatient treatment or sequenced treatment.
Those who receive continued inpatient treatment will stay in the hospital until they reach a healthy body weight and maintain it for 10 to 14 days. The average length of inpatient treatment will be 2 to 3 months. Those who receive sequenced treatment will transition to day patient status once they have met the following health benchmarks: an increase in body mass index (BMI) greater than 15.5 kg/m2; normal electrocardiograms, lab test results, and vital signs; eating all meals for more than 3 days; no weight loss for at least 1 week or weight gain for at least 1 week if the weight gain protocol has begun; and moderate improvement on a clinical global impression (CGI) rating of eating disorder behavior. If participants do not meet these benchmarks and are not at medical risk or suicidal, they will be automatically transitioned to day patient care after 28 days. Once participants reach the day patient status, they will be in the hospital Monday through Friday from 8:00 a.m. until 6:00 p.m. If these participants then reach and maintain a healthy body weight for 10 to 14 days, they will be transitioned to outpatient care, during which they will receive 50-minute therapy sessions once or twice weekly.
The aims and methods of treating anorexia will be the same for both groups. All participants will be prescribed meals, a snack, and dietary supplements in order to reach a healthy weight. The amount of exercise they engage in will be limited to ensure weight gain. Participants will also attend individual, family, and group therapy sessions aimed at supporting healthy thoughts and beliefs about eating behavior. Measurements of weight gain will be made every Monday, Wednesday, and Friday morning. Every 3 months participants will undergo blood tests and assessments of eating behaviors, associated psychopathology, and health service utilization. Clinical interviews will be conducted twice: once at study entry and once after 18 months.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Eating Disorders
Keywords
Anorexia Nervosa
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
41 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Continued inpatient treatment
Arm Type
Active Comparator
Arm Description
Participants will undergo inpatient hospital treatment until they have gained enough weight to be discharged.
Arm Title
Sequenced treatment
Arm Type
Experimental
Arm Description
Participants will begin with inpatient treatment, transition to day patient treatment, and then transition to outpatient treatment.
Intervention Type
Behavioral
Intervention Name(s)
Structured Behavioral Treatment
Intervention Description
Daily therapy sessions and a weight gain protocol involving set meals and exercise levels
Primary Outcome Measure Information:
Title
Weight
Time Frame
Measured over 18 months
Secondary Outcome Measure Information:
Title
Eating behaviors
Time Frame
Measured over 18 months
Title
Psychopathology associated with eating behaviors
Time Frame
Measured over 18 months
Title
Utilization of health care services
Time Frame
Measured over 18 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
16 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Diagnosis of anorexia nervosa, according to DSM-IV criteria
Body mass index (BMI) less than 18.5 kg/m2
Exclusion Criteria:
Presence of psychosis or the axis I disorders of schizophrenia, bipolar disorder, or active substance abuse or dependence requiring specialized treatment
Requires specialized treatment that is for major depression or anxiety disorders and is inconsistent with study treatments
Any major medical illness requiring immediate medical treatment or that would affect clinical treatment associated with the study
Significant risk of suicide
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Evelyn Attia, MD
Organizational Affiliation
Columbia University
Official's Role
Principal Investigator
Facility Information:
Facility Name
New York State Psychiatric Institute
City
New York
State/Province
New York
ZIP/Postal Code
10032
Country
United States
12. IPD Sharing Statement
Learn more about this trial
Effectiveness of High Intensity Inpatient Versus Stepped Intensity Treatment for Anorexia Nervosa
We'll reach out to this number within 24 hrs