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Integrative Cognitive-Affective Therapy for Binge Eating Disorder

Integrative Cognitive-Affective Therapy for Binge Eating Disorder

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02043496
Enrollment
96
Registered
2014-01-23
Start date
2013-12-31
Completion date
2017-08-31
Last updated
2020-07-17

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

Conditions

Binge Eating Disorder

Keywords

Binge Eating Disorder, Binge Eating, Eating Disorders, Obesity, Psychotherapy, Cognitive Behavioral Therapy

Brief summary

The purpose of the study is to test a newly developed individual psychotherapy treatment for binge eating disorder in adults. This treatment is a type of individual psychotherapy called Integrative Cognitive-Affective Therapy (ICAT) that focuses on helping people change their behaviors, feelings, thoughts about themselves, and relationships. This new treatment is being compared to an existing treatment called Cognitive-Behavior Therapy-Guided Self Help (CBTgsh), which focuses on changing behavior patterns through the use of reading and homework assignments along with sessions with a therapist. The primary hypothesis of this investigation is that ICAT will be associated with greater reductions in binge eating at end of treatment and follow-up compared to CBTgsh.

Interventions

BEHAVIORALIntegrative Cognitive-Affective Therapy

Integrative Cognitive-Affective Therapy is a psychotherapy treatment for binge eating that focuses on changing behaviors, feelings, thoughts, and relationships

BEHAVIORALCBT-Guided Self Help

CBT-Guided Self Help focuses on changing behavior patterns through the use of reading and homework assignments along with sessions with a therapist.

Sponsors

Neuropsychiatric Research Institute, Fargo, North Dakota
CollaboratorOTHER
University of Minnesota
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* Binge eating disorder (DSM-5)

Exclusion criteria

* History of gastric bypass surgery * Medical condition acutely affecting eating and/or weight * Current medical and/or psychiatric instability (e.g., acute suicidality) * Psychosis and/or bipolar disorder * Severe cognitive impairment or developmental disability * Inability to read English * Current substance use disorder * Current participation in psychotherapy and/or commercial weight loss program * Change in dosage and/or frequency of psychotropic medication in the past 6 weeks * Pregnant or breast feeding * BMI \< 21

Design outcomes

Primary

MeasureTime frameDescription
Binge Eating Episode Frequency (Eating Disorder Examination)17 Weeks and 6-month Follow-upFrequency of binge eating as measured by the Eating Disorder Examination

Secondary

MeasureTime frameDescription
Global Eating Disorder Symptoms (EDE)17 Weeks and 6-month follow-upGlobal Eating Disorder Symptoms as measured by the Eating Disorder Examination
Symptoms of Depression (BDI)17 Weeks and 6-month follow-upSymptoms of Depression as measured by the Beck Depression Inventory
Symptoms of Anxiety (STAI)17 Weeks and 6-month Follow-upSymptoms of Anxiety as measured by the State-Trait Anxiety Inventory
Self-Esteem (RSEQ)17 Weeks and 6-month Follow-upSelf-esteem as measured by the Rosenberg Self-Esteem Questionnaire

Countries

United States

Outcome results

None listed

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