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Focused Versus Enhanced Cognitive Behavioral Therapy for Treating Women With Bulimia Nervosa

Treatment of Bulimia Nervosa: Dysregulated Subtype

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00494858
Enrollment
50
Registered
2007-07-02
Start date
2007-07-01
Completion date
2012-12-01
Last updated
2026-07-20

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

Conditions

Eating Disorders

Keywords

Bulimia nervosa, Cognitive Behavioral Therapy, Personality Disorders

Brief summary

This study will compare the effectiveness of two types of cognitive behavioral therapy in treating adult women with the dysregulated subtype of bulimia nervosa.

Detailed description

Bulimia nervosa (BN) is a common eating disorder that is characterized by periods of bingeing and purging. People with the dysregulated subtype of BN experience behavioral impulsivity; disruption of cognitive, affective, behavioral, and neurophysiological processes (dysregulation); interpersonal dysfunction; and poor treatment response. To date, no therapies have been tested for this specific population, and it is unknown whether therapy that directly focuses on treating BN symptoms or one that addresses both eating and personality disorder symptoms is more effective. Cognitive behavioral therapy (CBT), which concentrates on modifying patients' behaviors and ways of thinking, has been effective in treating BN. This study will compare the effectiveness of two types of CBT, focused and broad, in treating adult women with the dysregulated subtype of BN. Participants in this single-blind study will be randomly assigned to receive 20 sessions of either broad (enhanced) or focused CBT. Participants will meet with a therapist once or twice weekly until 20 sessions have occurred. Broad CBT will address symptoms of BN, as well as those of the personality disorder. Focused CBT will concentrate only on BN symptoms. Before treatment begins, participants will complete a set of questionnaires pertaining to their experiences with BN, depression, anxiety, and interpersonal relationships. The questionnaires will be used throughout the study to assess participants' progress. Participants will also attend a clinical interview lasting approximately 3.5 hours. Questions will concern BN, other eating disorder symptoms, depression, anxiety, and interpersonal relationships. Blood samples and vital signs will also be taken at the time of the clinical interview and as needed later in the treatment process.

Interventions

BEHAVIORALCognitive behavioral therapy - focused (CBT-EF)

Focused CBT concentrates only on BN symptoms. There will be 20 sessions over the course of 5 months.

BEHAVIORALCognitive behavioral therapy - broad (EB)

Broad CBT addresses symptoms of BN, as well as those of the personality disorder. CBT-EB incorporates ED interventions from CBT-EF but also has modules focused on addressing mood intolerance and interpersonal difficulties. There will be 20 sessions over 5 months.

Sponsors

Boston University Charles River Campus
Lead SponsorOTHER
National Institute of Mental Health (NIMH)
CollaboratorNIH

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Diagnosis of bulimia nervosa * Presence of borderline personality disorder features * History of one mood or anxiety episode within 2 years prior to study entry * If taking psychiatric medication, dose has been stable for at least 6 weeks at time of study entry

Exclusion criteria

* Substance dependence * Diagnosis of bipolar I disorder * Psychosis * Mental retardation * Receiving psychosocial treatment

Design outcomes

Primary

MeasureTime frame
Eating disorder symptomsMeasured throughout the study

Secondary

MeasureTime frame
Depression symptomsMeasured throughout the study
Anxiety symptomsMeasured throughout the study
Interpersonal relationshipsMeasured throughout the study

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORHeather Thompson-Brenner, PhD

Center for Anxiety and Related Disorders, Boston University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 21, 2026