- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03637881
Cconsumer Perspective and Understanding of the Term "Milk" (CMK)
A Pilot Study Investigating Consumer Perspective and Understanding of the Term "Milk"
The objectives of this study are:
- To determine the consumption behaviors of dairy and non-dairy milks across a diverse demographic.
- To determine the purchasing behaviors of dairy and non-dairy milks across a diverse demographic.
- To determine the variation in medical history and health conditions amongst consumers of dairy milk and non-dairy milk alternatives.
- To assess the general knowledge and awareness of health associated with dairy milk and non-dairy milk alternatives.
Study Overview
Status
Conditions
Detailed Description
This study is an observational, cross-sectional trial design focused on obtaining information about consumer understanding and perception of the term "milk" and how they affect consumer choice.
A planned sample size of 50 will be enrolled into the study. This study will require one initial screening visit and 1 Study Day. This study will take approximately 2 to 2 ½ hours per subject to complete.
The initial screening visit will provide subject with the informed consent document and determine subject eligibility through anthropometric measurements, vital signs, and completion of an eating habits questionnaire.
If willing and eligible to participate, subjects will be invited to participate in the study for 1 Study Day that participants can choose to continue on to after the Screening visit.
Subject will arrive at the center in fasted for at least 2 hours or longer. During the Study Day, each participant will be asked to participate in two activities. In the first activity, participants will be presented with eight differently-labeled milk cartons, each accompanied by a fixed price label, and asked to answer questions regarding consumption. In the second activity, participants will be presented with the same setup from the first activity, however, the price labels for each product is varied according to real market prices for each product. In this activity, participants will be asked to answer questions regarding purchasing. Following these two activities, participants will then be asked to answer a questionnaire on consumer choice for dairy and non-dairy milk.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
Illinois
-
Chicago, Illinois, United States, 60616
- Clinical Nutrition Research Center
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Able to provide informed consent and comply with procedures
Exclusion Criteria:
- Under 18 years old
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
---|
Other
Daily or non-daily Consumers
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Data collection of consumption behaviors of dairy and non-dairy milks across a diverse demographic via questionnaire
Time Frame: 30 minutes
|
Consumption behaviors of dairy and non-dairy milks
|
30 minutes
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Data collection of purchasing behaviors of dairy and non-dairy milks across a diverse demographic via questionnaire
Time Frame: 30 minutes
|
Purchasing behaviors of dairy and non-dairy milks
|
30 minutes
|
Data collection of variations in medical history and health conditions amongst consumers of dairy milk and non-dairy milk alternatives via questionnaire
Time Frame: 30 minutes
|
variation in medical history and health conditions
|
30 minutes
|
Data collection of the general knowledge and awareness of health associated with dairy milk and non-dairy milk alternatives via questionnaire
Time Frame: 30 minutes
|
the general knowledge and awareness of health
|
30 minutes
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- IRB2018-069
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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