CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 253 enrolled
Drug / intervention
Devaluing energy-dense foods for cancer-controlbehavioral
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03557710
NCT03557710N/ACompleted

Devaluing Energy-dense Foods for Cancer-control: Translational Neuroscience

University of Oregon·interventional·Posted Jun 15, 2018·Updated Aug 14, 2023

In Brief

A clinical study evaluating Devaluing energy-dense foods for cancer-control for Overweight and Obesity and Cancer. Completed, enrolled 253 participants across 1 site.

Detailed Summary

Excessive eating of energy-dense foods and obesity are risk factors for a range of cancers. There are programs to reduce intake of these foods and weight loss, but the effects of the programs rarely last. This project tests whether altering the value of cancer-risk foods can create lasting change, and uses neuroimaging to compare the efficacy of two programs to engage the valuation system on a neural level. Results will establish the pathways through which the programs work and suggest specific treatments for individuals based on a personalized profile.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
20192020202120222023202420252026
First PostedJun 15, 2018
Enrollment StartMay 1, 2018
Primary CompletionMay 1, 2023
Study CompletionJun 30, 2023
TodayJul 2, 2026
Enrollment to primary: 5 yearsPosted 8.0 years ago

Interventions

Devaluing energy-dense foods for cancer-controlbehavioral

A 3-arm randomized controlled trial experiment study over 12 months. At baseline, participants will complete behavioral, neural, and self-report measures related to food, specifically measures of food valuation and of the proximal neural systems hypothesized to be linked to each of the 2 experimental arms. We will also measure food intake and body composition at baseline. Then participants will be randomized to one of 3 arms (2 experimental + 1 active control) for 8 30-min sessions to occur twice weekly at the University of Oregon for 30 days. At endpoint (\~1 month following baseline), all behavioral, neural, and self-report measures will be reassessed, as will eating, habit, and body composition measures. Follow-ups at 3, 6, and 12 months will assess all measures except neuroimaging.