- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06030687
FoodImage 3 Free-Living (FI3FL)
December 2, 2024 updated by: John Apolzan, Pennington Biomedical Research Center
Multiscale RECIPES (Resilient, Equitable, and Circular Innovations With Partnership and Education Synergies) for Sustainable Food Systems (FoodImage 3; FI3) Free-Living
Participants will be asked to use the app to capture data on food purchases, food waste that occurs during food preparation, food waste that is present after eating, and food waste from cabinet and refrigerator/freezer clean-outs.
During collection of much of the food waste data, participants will record in the app if food waste will be disposed of via composting, disposal, fed to pets, or garbage/landfill.
They will also indicate if the food was spoiled, past the expiration date, etc.
This will occur for 4-8 days.
Participants should perform the prep and eat occasions 4-8 days.
The shopping and toss occasions should be completed for at least 7 days.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Actual)
25
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
-
-
Louisiana
-
Baton Rouge, Louisiana, United States, 70808
- Pennington Biomedical 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
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Sampling Method
Probability Sample
Study Population
Healthy volunteers
Description
Inclusion Criteria:
- Male or Female, age 18-65 years
- Willing to be recontacted
- Conducts some of the food shopping, food purchasing, and/or food preparation for their household.
- Internet and/or Wi-Fi availability to complete surveys and send images.
- Ownership of an iPhone 9S or later, operable Apple ID, password, and email address that they are willing and able to use to collect data during the study. Subject acknowledges data usage and associated charges are a result of study.
- Willing to complete all study procedures and adhere to study visit timelines -
Exclusion Criteria:
- Refusal or unable to use an iPhone for study related purposes.
- Not willing to adhere to study procedures and study visit timelines.
- PBRC employee
- Any condition or circumstance that in the judgement of the PI could interfere with study participation
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
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Free-Living
|
Food purchase, prep, eat and toss data
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Total weight of household food waste
Time Frame: daily during baseline collection
|
weight (g)
|
daily during baseline collection
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Collaborators
Investigators
- Principal Investigator: John W Apolzan, PhD, Pennington Biomedical 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)
January 10, 2024
Primary Completion (Actual)
August 27, 2024
Study Completion (Actual)
August 27, 2024
Study Registration Dates
First Submitted
August 30, 2023
First Submitted That Met QC Criteria
September 7, 2023
First Posted (Actual)
September 11, 2023
Study Record Updates
Last Update Posted (Actual)
December 3, 2024
Last Update Submitted That Met QC Criteria
December 2, 2024
Last Verified
December 1, 2024
More Information
Terms related to this study
Other Study ID Numbers
- PBRC 2023-045 A
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
IPD Plan Description
Data may be requested.
The PI will be notified.
The proposed research question must be included.
All IPD that underlie results in a publication after a DTA with the institution may be requested.
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
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.