Improving eating behaviors in obesity through implicit priming
Neuronal and Behavioral Effects of an Implicit Priming Approach to Improve Eating Behaviors in Obesity
This study tests whether certain techniques can change how people with obesity think about food and help them eat better to lose weight.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 228 (estimated) |
| Ages | 18 Years to 65 Years |
| Sex | All |
| Sponsor | University of Colorado, Denver Academic / other |
| Locations | 1 site (Aurora, Colorado) |
| Trial ID | NCT05107908 on ClinicalTrials.gov |
What this trial studies
This study investigates how behavioral interventions, specifically implicit priming techniques, can influence food perceptions and eating behaviors in individuals with obesity. Participants will undergo different interventions aimed at altering their responses to food, while their brain activity and body weight changes will be monitored. The study aims to provide insights into the neural mechanisms underlying eating behaviors and how they can be modified to support weight loss.
Who should consider this trial
Good fit: Ideal candidates for this study are adults aged 18-65 with a BMI of 27 or greater.
Not a fit: Patients with contraindications for MRI or those who are pregnant may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could lead to effective strategies for improving eating behaviors and promoting weight loss in individuals with obesity.
How similar studies have performed: Other studies have shown promise in using behavioral interventions to modify eating behaviors, suggesting that this approach may be effective.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * 18-65 years old * BMI of 27 or greater Exclusion Criteria: * MRI contraindications (e.g., metal or electronic devices in the body) * Pregnancy
Where this trial is running
Aurora, Colorado
- University of Colorado Anschutz Medical Campus — Aurora, Colorado, United States (Recruiting)
Study contacts
- Principal investigator: Jason Tregellas, PhD — University of Colorado, Denver
- Study coordinator: Christina Erpelding, BS
- Email: christina.erpelding@cuanschutz.edu
- Phone: 303-724-8502
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.