Habituation Clinical Trial
Official title:
Repeated Food Exposure Via the Olfactory and Gustatory Systems
Verified date | April 2018 |
Source | The University of Tennessee, Knoxville |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Increasing exposure to a single orosensory cue without ingestion of additional energy may promote an increased rate of habituation, more rapid satiation, and reduced intake. This exposure can occur via smell (olfactory) and taste (gustatory) systems.It is not clear if repeated exposure via the combined olfactory and gustatory systems increases the rate of habituation more so than repeated exposure through one of these systems. Thus, the purpose of this investigation is to examine the amount of salivation occurring in 12 trials of exposure to a food via the olfactory, gustatory, and combined olfactory and gustatory systems. The primary dependent variable will be the amount of salivation in the 12 trials. It is hypothesized that a more rapid decrease in salivation will occur across trials in the combined olfactory and gustatory exposure as compared to the other two conditions, indicating a more rapid rate of habituation.
Status | Completed |
Enrollment | 27 |
Est. completion date | December 2015 |
Est. primary completion date | December 2015 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | 18 Years to 30 Years |
Eligibility |
Inclusion Criteria: - Dietary restraint scores of less than or equal to 12 on the Three Factor - - Eating Questionnaire-Cognitive Restraint scale. - Have a body mass index (BMI) between 18.5 and 24.9. Exclusion Criteria: - Are taking medications or having an illness which might influence salivation, smell, and taste (i.e. upper respiratory illness, methylphenidate, atropine, Benadryl, Elavil, etc) - Are currently dieting - Are a binge eater - Do not at least moderately like lemon or lime flavor scoring < 50 on a 100 mm visual analogue scale - Are a regular smoker - Have any dietary restrictions that will inhibit participation including food allergies |
Country | Name | City | State |
---|---|---|---|
United States | Healthy Eating and Activity Lab, University of Tennessee | Knoxville | Tennessee |
Lead Sponsor | Collaborator |
---|---|
The University of Tennessee, Knoxville |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Amount of Salivation | 12 trials (90 minutes) |
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