Flavor Test Results in General Population
|
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. |
| ClinicalTrials.gov Identifier: NCT03506074 |
|
Recruitment Status :
Completed
First Posted : April 23, 2018
Last Update Posted : April 24, 2018
|
- Study Details
- Tabular View
- No Results Posted
- Disclaimer
- How to Read a Study Record
Dietary choices are influenced by several factors, including physiological, social or genetic factors. Among these, flavor is the most important determinant modulating the preferences versus specific foods.
Flavor perception is the result from the sensory integration of taste and odor properties of food.
Aim of the present study was to assess flavor abilities in a large population using a validated perceptive test.
| Condition or disease | Intervention/treatment |
|---|---|
| Weight, Body Smoking Age Problem | Diagnostic Test: Flavor test |
This protocol investigates flavor perception using the flavor test, a specific test to assess the retro-nasal olfactory function.
A decrease in taste and smell abilities can result in loss of appetite, inadequate dietary intake and malnutrition. Several diseases and conditions have been associated with taste disorders and a decline in gustatory function is very common in the elderly.
The flavor test was previously developed, validated and patented by our group. It consists of a series of 20 aromatic extracts, corresponding to routine dietary use flavors for Italian people.
Each tastant, originally stored in a 30 mL amber bottle, is diluted in distilled water and stored at 4 °C, then it is kept at room temperature for 20 min before administration.
An aliquot of approximately 0,5 mL of each tastant is administered in the oral cavity using a 3mL Transfer Pipet and left for approximately 5 seconds; the mouth is then rinsed twice with distilled water before the administration of the following tastant.
At each administration, participants are invited to identify the aromatic by making a choice from 5 proposed items. A total of 21 aromatics (including one blank) are administered sequentially. The flavor score (FS) is calculated as the sum of correctly identified aromatics and ranged from 0 to 21.
| Study Type : | Observational |
| Actual Enrollment : | 420 participants |
| Observational Model: | Cohort |
| Time Perspective: | Cross-Sectional |
| Official Title: | Flavor Perception in the Population of Campania Region, Italy |
| Actual Study Start Date : | October 1, 2014 |
| Actual Primary Completion Date : | October 30, 2017 |
| Actual Study Completion Date : | October 30, 2017 |
| Group/Cohort | Intervention/treatment |
|---|---|
|
General population
Adult volunteers (≥18 years of age) selected as part of a project to investigate the role of lifestyle in preventing chronic diseases supported by the Campus Salute association (www.campussalute.it). All volunteers performed the flavor test as described in Maione et al, Endocrine, 2016 (doi:10.1007/s12020-015-0690-y). |
Diagnostic Test: Flavor test
The flavor test was developed, validated and patented (patent no. 0001426253 of the Italian Ministry for the Economic Development). It consists of a series of 20 aromatic extracts, corresponding to routine dietary use flavors for Italian people. At each administration, participants were invited to identify the aromatic by making a choice from 5 proposed items. A total of 21 aromatics (including one blank) were administered sequentially. The flavor score (FS) was calculated as the sum of correctly identified aromatics and ranged from 0 to 21. |
- Flavor score [ Time Frame: Immediately after the test administration flavor score was calculated ]A flavor score (1-21) was measured in all the studied subjects using the Flavor test
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
| Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
| Sexes Eligible for Study: | All |
| Sampling Method: | Non-Probability Sample |
Inclusion Criteria:
Age ≥ 18 years
Exclusion Criteria:
Allergies, drug usage
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03506074
| Principal Investigator: | Paolo E. Macchia, M.D., Ph.D. | Dipartimento Medicina Clinica e Chirurgia, Università degli Studi di Napoli Federico II |
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
| Responsible Party: | Paolo Emidio Macchia, Prof., Federico II University |
| ClinicalTrials.gov Identifier: | NCT03506074 |
| Other Study ID Numbers: |
PM0001/18 |
| First Posted: | April 23, 2018 Key Record Dates |
| Last Update Posted: | April 24, 2018 |
| Last Verified: | April 2018 |
| Individual Participant Data (IPD) Sharing Statement: | |
| Plan to Share IPD: | No |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | No |
|
Obesity Flavor |
|
Body Weight |

