Computerized Response Training Obesity Treatment
NCT03375853 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 179
Last updated 2023-09-26
Summary
This project will test whether a food response training intervention produces lasting body fat loss, use objective brain imaging to examine the mechanism of effect of this treatment and investigate the generalizability of the training to non-training foods, and examine factors that should amplify intervention effects to provide a test of the intervention theory. This novel treatment represents a bottom-up implicit training intervention that does not rely on executive control, prolonged caloric deprivation, and expensive clinicians to deliver, like behavioral weight loss treatments that have not produced lasting weight loss. If this computer-based response training intervention produces sustained body fat loss in overweight individuals, it could be easily implemented very broadly at almost no expense, addressing a leading public health problem.
Conditions
- Obesity
- Hyperphagia
- Feeding and Eating Disorders
Interventions
- BEHAVIORAL
-
Computer Based Response Training Weight Loss Intervention
Participants complete four computer based training tasks each visit, over the course of a few lab visits. Participants then perform weekly booster sessions in a more natural home or community environment over the internet using the same computer based training tasks.
- BEHAVIORAL
-
Generic Response Training Control Intervention
Participants complete four computer based training tasks each visit, over the course of a few lab visits. Participants then perform weekly booster sessions in a more natural home or community environment over the internet using the same computer based training tasks.
Sponsors & Collaborators
-
Flinders University
collaborator OTHER -
University of Exeter
collaborator OTHER -
Radboud University Medical Center
collaborator OTHER -
University of Oregon
collaborator OTHER -
Oregon Research Institute
lead OTHER
Principal Investigators
-
Eric Stice, PhD · Stanford University
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- SINGLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Max Age
- 38 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2017-07-15
- Primary Completion
- 2023-08-31
- Completion
- 2023-09-15
Countries
- United States
Study Locations
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