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Brain's Response to Chocolate

Behavioral Assessment of the Brain Response to Bioactive Food Components Using Electroretinography (Brain's Response to Chocolate)

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03364413
Enrollment
20
Registered
2017-12-06
Start date
2018-01-17
Completion date
2018-03-02
Last updated
2023-12-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Overweight, Obesity

Brief summary

The purpose of this study is to test how the brain responds when individuals eat enjoyable foods such as chocolate. Eating certain foods can make one want to keep eating even when feeling full, caused by dopamine in the brain. The researchers believe this dopamine response can be measured by looking at the individual's eye.

Detailed description

With obesity at an all-time high, understanding eating behavior beyond physical need is a priority. Food reinforcement is driven by central dopamine activity. However, objective measurement of brain dopamine-related behavioral events is hindered by the lack of non-invasive, accessible techniques that are amenable to testing in a naturalistic environment. The goal of this project is to develop a non-invasive, accessible methodology to measure dopaminergic responses to food in a natural setting. This research will use a novel, hand-held electroretinograph (ERG) that does not require eye dilation and uses a skin electrode to measure retinal dopamine activity. Previous work establishes that retinal dopamine activity can be used as a proxy for central dopamine function. The ability to assess both subjective behavioral variables and central dopaminergic responses simultaneously will provide an ideal approach for innovative studies of the control of eating behavior.

Interventions

Participants will be asked to taste commercially available chocolate varying in sugar, fat and percent cocoa (milk, 70%, 85% and 90% cocoa).

Sponsors

Drexel University
CollaboratorOTHER
USDA Grand Forks Human Nutrition Research Center
Lead SponsorFED

Study design

Observational model
COHORT
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Age
18 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

* body mass index 20-30 kg/m2 * free of any major illness or disease

Exclusion criteria

* food allergies * participation in a weight loss diet or exercise program * pregnancy * lactation * metabolic illness or disease (diabetes, renal failure, thyroid illness, hypertension) * eye illness or disease (narrow angle glaucoma, macular degeneration, retinal detachment, cataracts) * psychiatric, neurological or eating disorders (schizophrenia, depression, Parkinson's Disease, Huntington's Disease, cerebral palsy, stroke, epilepsy, anorexia nervosa or bulimia nervosa) * take prescription medications except for oral contraceptives or antihyperlipidemia agents

Design outcomes

Primary

MeasureTime frameDescription
Retinal dopamine response to oral stimuli30 minutesElectroretinograph beta wave amplitude will increase in response to increases in the amount of sugar in the chocolate
Psychoactive Effects Questionnaire in response to oral stimuli30 minutesThe number of positive responses on the Psychoactive Effects Questionnaire will increase in response to increases in the sugar content of the chocolate

Secondary

MeasureTime frameDescription
Scores on the Binge Eating Scale will correlate with the retinal dopamine and Psychoactive Effect Questionnaire responses30 minutesIndividual changes in the retinal dopamine response and the number of positive responses on the Psychoactive Effects Questionnaire will correlate with individual scores on the Binge Eating Scale

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026