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Clinical Trials/NCT03261050
NCT03261050
Completed
Not Applicable

Target Engagement of a Novel Dissonance-Based Treatment for DSM-5 Eating Disorders

Stanford University2 sites in 1 country83 target enrollmentJuly 10, 2017
ConditionsEating Disorder

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Eating Disorder
Sponsor
Stanford University
Enrollment
83
Locations
2
Primary Endpoint
Change in occurrences of binge eating episodes using Eating Disorder Diagnostic Interview
Status
Completed
Last Updated
10 months ago

Overview

Brief Summary

Most people with an eating disorder (ED) do not receive good treatment. The investigators have developed a new brief group treatment that is supposed to work by reducing how much women with an ED value the impossible thinness standard promoted by the media and how much they value/crave binge foods. The investigators want to test whether the treatment actually changes those two mechanisms using brain scan data, which is more objective than completing questionnaires and even interviews.

In the first phase of the study (R61), the investigators will compare women in the treatment versus those on a wait-list. If the investigators can show that the treatment "works" (does what the investigators think it does) compared to no active treatment (women will be allowed to seek and receive outside help but investigators will not provide it until after the wait-list), investigators will conduct the second phase of study (R33),where they will randomly assign women with an ED to either the new treatment or to a group treatment that represents what many college mental health clinics provide to their clients with ED.

Detailed Description

Only 3-20% of individuals with eating disorders (EDs) receive treatment, and those who do rarely receive evidence-based treatments because they are very intensive and costly, few clinicians deliver them, and they differ for the various EDs. These factors have hindered broad implementation of evidence-based treatments, implying that a brief frontline outpatient treatment for a range of EDs that could be easily, cheaply, and widely implemented would address a major public health problem. There is also limited experimental evidence regarding factors that maintain EDs and mechanisms of action for ED treatments. The investigators propose to conduct a project that translates basic persuasion research into clinical hypotheses and a novel treatment. The investigators hypothesize that EDs are maintained by (1) excessive valuation of the thin beauty ideal, which prompts caloric restriction and other unhealthy weight control behaviors (vomiting, laxative use, excessive exercise) that increase binge eating risk, and (2) excessive valuation of high-calorie foods, which maintains binge eating. The investigators propose to evaluate a treatment that addresses these hypothesized maintenance processes. Two pilot trials evaluated a novel 8-session group dissonance-based treatment (Counter Attitudinal Therapy; CAT) wherein women with any ED appropriate for outpatient care completed activities in which they collectively discuss costs of pursuing the thin ideal and the ED behaviors in which they personally engage (unhealthy weight control behaviors and binge eating), which putatively creates dissonance about engaging in those particular behaviors that reduce valuation of the thin ideal and high-calorie binge foods. During the COVID-19 shelter-at-home orders taking place at both research sites, the investigators will not measure in-person only outcomes including fMRI, ECG, computerized implicit associated tests, and height and weight measurements for all participants that have assessments during this order. The investigators will continue to conduct treatment groups that will be administered on a virtual platform.

Registry
clinicaltrials.gov
Start Date
July 10, 2017
End Date
January 31, 2025
Last Updated
10 months ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Eric Stice

Professor of Psychiatry and Behavioral Sciences

Stanford University

Eligibility Criteria

Inclusion Criteria

  • DSM-5 eating disorder
  • Must have a primary care doctor

Exclusion Criteria

  • Non-English speakers
  • BMI \<75% ideal body weight
  • Current acute suicidal ideation (defined as thoughts of a specific method or plan)
  • Comorbid psychiatric disorder that would disrupt groups (e.g., bipolar disorder, substance misuse)
  • Serious medical problems (e.g., diabetes)

Outcomes

Primary Outcomes

Change in occurrences of binge eating episodes using Eating Disorder Diagnostic Interview

Time Frame: Week 8; R33 also reviews at 6-month follow-up

Interviewer assesses frequency in binge eating episodes

Change in psychosocial impairment due to eating disorder symptoms using the Clinical Impairment Assessment Questionnaire

Time Frame: Week 8; R33 also reviews at 6-month follow-up

Interviewer assesses change in psychosocial impairment

Change in occurrences of compensatory weight control behavior using Eating Disorder Diagnostic Interview

Time Frame: Week 8; R33 also reviews at 6-month follow-up

Interviewer assesses frequency of compensatory weight control behaviors

Secondary Outcomes

  • Change in valuation of thin ideal using the Thin Ideal Valuation Scale(Weeks 2, 4, 6, and 8; R33 also reviews at 6-month follow-up)
  • Change in reward region of the brain using fMRI(Week 1 and Week 8)
  • Change in body dissatisfaction using the Body Dissatisfaction Scale(Weeks 2, 4 and 6)
  • Change in suicidal ideation/attempts using the Patient Health Questionnaire version 9 (PHQ-9)(Weeks 2, 4 and 6)
  • Change in negative affect using the Positive Affect and Negative Affect Scale-Revised(Weeks 2, 4, and 6)
  • Change in implicit associations of binge foods, thin models, and eating disorder behavior words(Week 8; R33 also reviews at 6-month follow-up)
  • Change in food addiction using the Yale Food Addiction Scale version 2.0(Weeks 2, 4, and 6)
  • Change in dietary restraint using the 10-item Dutch Restrained Eating Scale(Week 8; R33 also reviews at 6-month follow-up)

Study Sites (2)

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