- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04858971
Survey of Diet and Health Beliefs
May 13, 2024 updated by: USDA Grand Forks Human Nutrition Research Center
Effect of Dietary Advice Source on Perceptions of Information Accuracy and Intended Compliance
The purpose of this research is to better understand people's health and diet knowledge, beliefs, attitudes, and practices.
The researchers will use this information to implement better strategies to help Americans maintain more nutritious diets.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
The overall goal of this study is to determine whether there are differences in perceptions of healthy nutrition messages depending on from whom the message is coming.
More specifically, the researchers aim to examine whether there are differences in how people perceive and intend to follow nutrition information that is coming from a variety of sources.
Study Type
Observational
Enrollment (Actual)
1000
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
North Dakota
-
Grand Forks, North Dakota, United States, 58203
- USDA Grand Forks Human Nutrition Research Center
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 99 years (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Sampling Method
Non-Probability Sample
Study Population
Participants will include American adults aged 18 and over.
Minors, i.e., those under 18, will be excluded.
To participate, people must have access to internet.
Therefore, by default, those who do not have internet access will be excluded from this study.
Due to the nature of this study, participants from all over the country will be eligible to participate.
Description
Inclusion Criteria:
- US citizen
- have access to internet
- have an Amazon Mechanical Turk (MTurk) account
Exclusion Criteria:
- under 18 years of age
- no access to internet
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Case-Control
- Time Perspectives: Cross-Sectional
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Control
No source will be indicated on information provided for review
|
Participants will see the same health advice, with no source or one of three other sources indicated
|
|
Government source
A government logo will be shown on information provided for review
|
Participants will see the same health advice, with no source or one of three other sources indicated
|
|
Medical source
A medical logo will be shown on information provided for review
|
Participants will see the same health advice, with no source or one of three other sources indicated
|
|
Social media source
A social media logo will be shown on information provided for review
|
Participants will see the same health advice, with no source or one of three other sources indicated
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Perception of health information
Time Frame: Baseline
|
Participants will rate the extent to which they trust the source of health information (i.e., the makers of the flyer) on a 7-point Likert-type scale ranging from not at all (1) to completely (7).
|
Baseline
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Alese Nelson, PhD, USDA Grand Forks Human Nutrition Research Center
- Principal Investigator: James Roemmich, PhD, USDA Grand Forks Human Nutrition Research Center
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
June 21, 2021
Primary Completion (Actual)
September 24, 2021
Study Completion (Actual)
September 24, 2021
Study Registration Dates
First Submitted
April 21, 2021
First Submitted That Met QC Criteria
April 21, 2021
First Posted (Actual)
April 26, 2021
Study Record Updates
Last Update Posted (Actual)
May 16, 2024
Last Update Submitted That Met QC Criteria
May 13, 2024
Last Verified
May 1, 2024
More Information
Terms related to this study
Other Study ID Numbers
- GFHNRC337
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
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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