Although taste influences food choices and favours diseases like obesity, there is no consensus about the existence of correlations between bitterness and anthropometric variables. Also, an electronic-based method for data collection could provide a more appropriate way for the evaluation of taste perception and save time.
The objective is to search for correlations between bitterness and anthropometric variables.
Full Title of Study: “Anthropometric Variables and Perception of Bitter Taste in Obese Adults or Not”
- Study Type: Observational
- Study Design
- Time Perspective: Cross-Sectional
- Study Primary Completion Date: January 31, 2016
A cross-sectional study evaluating correlations between the bitterness rates given on a generalized Labeled Magnitude Scale, anthropometrics and other variables. Bitterness perceptions at the tip of the tongue (TOTp) and at the whole mouth (WMp) were recorded using a locally developed novel cloud-based software (Cloud-gLMS). The ANCOVA test was adjusted using TOTp and WMp as dependent variables and age, height, weight, BMI, gender, waist circumference, alcohol intake, comorbidities, and use of medications as independent variables.
Arms, Groups and Cohorts
- Evaluation of bitter taste
- Participants will be evaluated as to the intensity of bitter taste when performing watery mouthwash with quinine.
Clinical Trial Outcome Measures
- Sensitivity of bitter taste 1
- Time Frame: 1 time
- It will be gently applied at the end of the tongue, by means of a swab soaked in the quinine solution at room temperature, in continuous movements from left to right, and will point a note to the bitter level.
- Sensitivity of bitter taste 2
- Time Frame: 1 time
- The volunteer will perform a “mouthwash” with the quinine solution, and will point a note to the bitter level.
Participating in This Clinical Trial
- Weight limit of 150 kg and who are able to read the text with the guidelines on how to be punctuated the sensation of bitter in the generalized labeled scale.
- Being a relative of the first degree of a patient already included in the research, tobacco in the forms of cigarettes, pipes and cigars in the last 30 days, presence of coryza, nasal congestion or frequent sneezing, dental treatment on the same day of the research. Being a dementia sufferer, having an altered, drowsy level of consciousness. Show upper limb tremor visible.
Gender Eligibility: All
Minimum Age: 18 Years
Maximum Age: 59 Years
Are Healthy Volunteers Accepted: Accepts Healthy Volunteers
- Lead Sponsor
- University of Sao Paulo
- Provider of Information About this Clinical Study
- Principal Investigator: Julio Sergio Marchini, Principal Investigator – University of Sao Paulo
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