Food Response Training for Binge Eating

Sponsor
Loma Linda University (Other)
Overall Status
Terminated
CT.gov ID
NCT02817412
Collaborator
Oregon Research Institute (Other)
35
1
4
22.7
1.5

Study Details

Study Description

Brief Summary

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

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Go/No-Training
  • Behavioral: Stop-Signal Training
  • Behavioral: Dot-Probe Paradigm
  • Behavioral: Generic Response Training
N/A

Detailed 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.

Study Design

Study Type:
Interventional
Actual Enrollment :
35 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Food Response Training for Binge Eating
Actual Study Start Date :
Jun 1, 2016
Actual Primary Completion Date :
Apr 24, 2018
Actual Study Completion Date :
Apr 24, 2018

Arms and Interventions

Arm Intervention/Treatment
Experimental: Go/No-Go Training

In the go/no go training, participants are shown images in which high-calorie foods are shown on one side of the screen and low-calorie foods on the other. They are told to press response keys as quickly as possible to indicate the side of presentation (go-trials). On half of the trials, the rectangular frame surrounding the image is not solid but hatched, which is a signal for them to withhold their response (no-go trials). This training is divided into 4 blocks of 50 trials.

Behavioral: Go/No-Training

Experimental: Stop-Signal Training

In the stop signal training, participants are shown images in either a dark blue or light gray border. They are told to press the space bar as quickly as possible when the border is blue (go trials) and to withhold a response when the border is gray (no-go trials). This training is divided into 20 blocks of 32 trials.

Behavioral: Stop-Signal Training

Experimental: Dot-Probe Training

In the dot-probe training, participants are shown images in which high-calorie foods are shown on one side of the screen and low-calorie foods on the other. Immediately after the images disappear, a small dot probe appears in the location of one of the images. Participants are told to press response keys as quickly as possible to indicate whether a visual probe appeared behind the left or right image during the trials. The probe appears in the location occupied by a high-calorie food image 10% of the time and in the location occupied by a low-calorie food image 90% of the time. This training is divided into 6 blocks of 40 trials.

Behavioral: Dot-Probe Paradigm

Placebo Comparator: Generic Training

In the generic training, participants complete a generic go/no-go training that uses images of flowers and office supplies instead of the images of high-calorie and low-calorie food images. This generic go/no go training is identical in duration and contact time to the go/no-go food training.

Behavioral: Generic Response Training

Outcome Measures

Primary Outcome Measures

  1. Binge Eating Frequency [Post-intervention (at 4 months)]

    Number of times engaged in binge eating (self-report)

  2. Binge Eating Frequency [3-month follow-up (at 7 months)]

    Number of times engaged in binge eating (self-report)

Secondary Outcome Measures

  1. Body Mass Index [Post-intervention (at 4 months)]

    Weight in kilograms divided by height in meters squared.

  2. Body Mass Index [3-month follow-up (at 7 months)]

    Weight in kilograms divided by height in meters squared.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 55 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Sylvia Herbozo Chicago Illinois United States 60607

Sponsors and Collaborators

  • Loma Linda University
  • Oregon Research Institute

Investigators

  • Principal Investigator: Sylvia Herbozo, Ph.D., University of Illinois at Chicago

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Holly Morrell, Associate Professor, Loma Linda University
ClinicalTrials.gov Identifier:
NCT02817412
Other Study ID Numbers:
  • 5160020
First Posted:
Jun 29, 2016
Last Update Posted:
Nov 25, 2019
Last Verified:
Nov 1, 2019
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Keywords provided by Holly Morrell, Associate Professor, Loma Linda University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 25, 2019