MedPath

Using EEG Operant Conditioning to Improve Trait Self-Control and Promote Healthy Behavior

Phase 1
Completed
Conditions
Obesity
Type II Diabetes
Cardiovascular Disease
Health Behavior
Registration Number
NCT01801254
Lead Sponsor
University of Rochester
Brief Summary

The field of neuroeconomics has begun to elucidate neural mechanisms underlying self-control; however, researchers have not yet harnessed neuroeconomics findings to develop interventions for improving self-control ability. The investigators are currently developing such an intervention. The investigators' approach involves using a brain-computer interface with audiovisual feedback to show people what is happening in their own brains, in real time. Through this interface, individuals are trained to increase levels of neural activity that may facilitate self-control, which, in turn, may improve the ability to exhibit self-controlled behaviors. This may increase the ability to engage in heath behaviors for which self-control is required (eg, dieting and exercising). The investigators' long-term goal is to create a tool that will help people develop the self-control needed to achieve lasting improvements in health behaviors.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
16
Inclusion Criteria
  • Can read and write fluently in English
  • At least 18 years of age
  • Right-handed
  • Overweight or obese (BMI > 24.9)
  • Currently has a University of Rochester meal plan
  • Currently in contemplation or action stages of change with respect to weight loss (measured with the Weight Stages of Change Algorithm; Rossi, Rossi, Velicer, & Prochaska, 1995).
Exclusion Criteria
  • History of diabetes, epilepsy, celiac disease, lactose intolerance, food allergies, veganism, mental illness, or eating disorders
  • Currently taking a medication that may have a strong effect on EEG recordings (eg, an antidepressant, stimulant medication, etc.)
  • Currently drinks more than 3 cups of coffee per day or roughly equivalent caffeine intake

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
postprandial blood glucose and triglycerides4 times per week for 4 weeks
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

University of Rochester

🇺🇸

Rochester, New York, United States

University of Rochester
🇺🇸Rochester, New York, United States

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