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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT02817412
Other study ID # 5160020
Secondary ID
Status Terminated
Phase N/A
First received
Last updated
Start date June 2016
Est. completion date April 24, 2018

Study information

Verified date November 2019
Source Loma Linda University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study will examine the effectiveness of food response training interventions in reducing binge eating among adults engaged in binge eating.


Description:

Binge eating disorder is the most prevalent eating disorder and affects both men and women at comparable rates unlike anorexia nervosa and bulimia nervosa. Given that binge eating and obesity are strongly associated, binge eating treatments should aim to reduce binge eating as well as weight. However, most binge eating interventions do not produce lasting weight loss. Recent research has shown computer-based response inhibition training with high-calorie foods reduces reward region response to and attentional bias for the training foods, decreases training food intake, increases inhibitory control, and produces weight loss in overweight adults. There is evidence that the weight loss effects from such response training persist through 6-month follow-up. Further, binge eating has been associated with increased food-related impulsivity and increased activation in a reward-processing brain region to high-calorie foods. Prior research suggests that food response training may be an effective intervention for binge eating that teaches automatic self-control in response to high-calorie foods which in turn, reduces binge eating and produces weight loss. This study will examine the effectiveness of food response training interventions in reducing binge eating and weight among adults engaged in binge eating.

The goals of this study are to: (1) test the hypothesis that adults who complete the food response trainings will show significantly greater reductions in binge eating frequency and in body mass index (BMI) compared to generic response training from pretest to posttest and at 3-month follow up, (2) to determine whether one of the food response trainings is more effective in binge eating frequency and reducing BMI from pretest to posttest and at 3-month follow up, and (3) test whether a reduction in valuation of the high-calorie versus low-calorie foods (willingness to pay for the pictured foods) and/or behavioral improvement of inhibitory control during the training tasks mediate the effects of the various trainings on reductions in binge frequency and body mass index.


Recruitment information / eligibility

Status Terminated
Enrollment 35
Est. completion date April 24, 2018
Est. primary completion date April 24, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 55 Years
Eligibility Inclusion Criteria:

- Engages in objective binge episodes as defined by the Diagnostic and Statistical Manual of Mental Disorders (DSM-5) and meets one of the following frequency and duration criteria: 1) at least two objective binge episodes per month for at least 3 months; or 3) at least six objective binge episodes over a shorter period

Exclusion Criteria:

- Illicit drug use and excessive alcohol use

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Go/No-Training

Stop-Signal Training

Dot-Probe Paradigm

Generic Response Training


Locations

Country Name City State
United States Sylvia Herbozo Chicago Illinois

Sponsors (2)

Lead Sponsor Collaborator
Loma Linda University Oregon Research Institute

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Binge Eating Frequency Number of times engaged in binge eating (self-report) Post-intervention (at 4 months)
Primary Binge Eating Frequency Number of times engaged in binge eating (self-report) 3-month follow-up (at 7 months)
Secondary Body Mass Index Weight in kilograms divided by height in meters squared. Post-intervention (at 4 months)
Secondary Body Mass Index Weight in kilograms divided by height in meters squared. 3-month follow-up (at 7 months)
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