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Clinical Trials/NCT04037020
NCT04037020
Completed
Not Applicable

Assessment of Dopaminergic Neurotransmission in Response to Tasting Chocolate (The Chocolate Study 2.0)

USDA Grand Forks Human Nutrition Research Center1 site in 1 country20 target enrollmentJuly 25, 2019
ConditionsNormal Weight

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Normal Weight
Sponsor
USDA Grand Forks Human Nutrition Research Center
Enrollment
20
Locations
1
Primary Endpoint
Retinal dopamine response to oral stimuli
Status
Completed
Last Updated
last year

Overview

Brief Summary

The purpose of this study is to test how the brain responds when enjoyable foods such as chocolate are consumed. The investigators know that eating certain types of foods can make an individual want to keep eating even when he or she is full. The chemical in the brain that causes this is called dopamine. The investigators can measure this response by looking at changes to how an individual's eye responds to light.

Detailed Description

The overall objective of this study is to determine dopamine (DA) neuromodulation (changes in b-wave amplitude as measured by electroretinography (ERG)) in response to consuming a highly reinforcing food (chocolate). The investigators hypothesize that orosensory stimulation with chocolates with increasing sugar content will increase the beta wave (b-wave) amplitude and the increase in the b-wave amplitude will correlate with score changes on the Psychophysical Effects Questionnaire (PEQ). This will be accomplished by testing different chocolates (extreme dark (90% cocoa), dark (70% cocoa), milk (38% cocoa), and white (0% cocoa)) on different days using 1.0 cd∙s/m2 flash luminance energy.

Registry
clinicaltrials.gov
Start Date
July 25, 2019
End Date
September 5, 2019
Last Updated
last year
Study Type
Observational
Sex
All

Investigators

Sponsor
USDA Grand Forks Human Nutrition Research Center
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • BMI 20-24.9 kg/m2
  • ability to understand and sign the consent form
  • availability of transportation (i.e., participants must be able to provide their own transportation to the Grand Forks Human Nutrition Research Center)
  • be free of any major illness/disease

Exclusion Criteria

  • food allergies
  • participation in a weight loss diet/exercise program
  • pregnancy
  • lactation
  • metabolic illness/disease (diabetes, renal failure, thyroid illness, hypertension)
  • eye illness/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)
  • taking any type of prescription medication with the exception of oral contraceptives and antihyperlipidemia agents

Outcomes

Primary Outcomes

Retinal dopamine response to oral stimuli

Time Frame: 30 minutes

Electroretinograph b-wave amplitude will increase in response to increases in the amount of sugar in the chocolate.

Secondary Outcomes

  • Correlation between b-wave amplitude and PEQ scores(30 minutes)
  • Correlation between b-wave amplitude and habitual dietary intake(30 minutes)

Study Sites (1)

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