The classic website will no longer be available as of June 25, 2024. Please use the modernized ClinicalTrials.gov.
Working…
ClinicalTrials.gov
ClinicalTrials.gov Menu

FoodImage 3 Laboratory (FI3Lab)

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. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT06030700
Recruitment Status : Recruiting
First Posted : September 11, 2023
Last Update Posted : January 12, 2024
Sponsor:
Collaborator:
Martin, Corby, K., M.D.
Information provided by (Responsible Party):
John Apolzan, Pennington Biomedical Research Center

Study Description
Go to 
Top of Page Study Description Study Design Groups and Cohorts Outcome Measures Eligibility Criteria Contacts and Locations More Information
Brief Summary:
The Laboratory Study will be conducted at PBRC and will include participants (N=25) from a wide array of social and economic groups will be recruited and trained on the use of the FoodImage app. Participants use the app to measure food waste (including foods with inedible parts) created during a simulated meal preparation setting, a simulated meal consumption setting with plate waste, and a simulated cabinet and refrigerator clean-out of spoiled and out-of-date foods, where the number of items and the amounts of waste for each task is randomly assigned across participants and blinded from the research staff evaluating images and coding data. These participants will denote the normal discard destination (I.e., garbage, sink/disposal, feed to animal, compost) for each item as if the waste had occurred in their own home.

Condition or disease Intervention/treatment
Waste Management Food Supply Other: Controlled Conditions

Study Design
Go to 
Top of Page Study Description Study Design Groups and Cohorts Outcome Measures Eligibility Criteria Contacts and Locations More Information

Layout table for study information
Study Type : Observational
Estimated Enrollment : 25 participants
Observational Model: Case-Control
Time Perspective: Prospective
Official Title: Multiscale RECIPES (Resilient, Equitable, and Circular Innovations With Partnership and Education Synergies) for Sustainable Food Systems (FoodImage 3; FI3) Laboratory
Actual Study Start Date : January 10, 2024
Estimated Primary Completion Date : December 31, 2024
Estimated Study Completion Date : April 15, 2025
Groups and Cohorts
Go to 
Top of Page Study Description Study Design Groups and Cohorts Outcome Measures Eligibility Criteria Contacts and Locations More Information

Group/Cohort Intervention/treatment
Laboratory
Simulated kitchen setting including purchase, prep, eating and cleanout
 Other: Controlled Conditions
Use of FoodImage app to take pictures of food and/or receipts.


Outcome Measures
Go to 
Top of Page Study Description Study Design Groups and Cohorts Outcome Measures Eligibility Criteria Contacts and Locations More Information

Primary Outcome Measures :
  1. Weight of Food Waste [ Time Frame: At Baseline Laboratory Study Visit ]
    Weight (g)


Eligibility Criteria
Go to 
Top of Page Study Description Study Design Groups and Cohorts Outcome Measures Eligibility Criteria Contacts and Locations More Information

Information from the National Library of Medicine

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.


Layout table for eligibility information
Ages Eligible for Study:   18 Years to 65 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Sampling Method:   Probability Sample
Study Population
Healthy Volunteers
Criteria

Inclusion Criteria:

  • Male or female, age 18-65 years
  • Willing to be recontacted

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
Contacts and Locations
Go to 
Top of Page Study Description Study Design Groups and Cohorts Outcome Measures Eligibility Criteria Contacts and Locations More Information

Information from the National Library of Medicine

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): NCT06030700


Contacts
Layout table for location contacts
Contact: John W Apolzan, PhD 2257632827 john.apolzan@pbrc.edu
Contact: Rob Leonard 225-763-0948 doctors@pbrc.edu

Locations
Layout table for location information
United States, Louisiana
Pennington Biomedical Research Center Recruiting
Baton Rouge, Louisiana, United States, 70808
Contact: John W Apolzan, PhD    225-763-2827    john.apolzan@pbrc.edu   
Principal Investigator: John W Apolzan, PhD         
Principal Investigator: Corby K Martin, PhD         
Sponsors and Collaborators
Pennington Biomedical Research Center
Martin, Corby, K., M.D.
Investigators
Layout table for investigator information
Principal Investigator: John W Apolzan, PhD Pennington Biomedical Research Center
More Information
Go to 
Top of Page Study Description Study Design Groups and Cohorts Outcome Measures Eligibility Criteria Contacts and Locations More Information
Layout table for additonal information
Responsible Party: John Apolzan, Associate Professor-Research, Pennington Biomedical Research Center
ClinicalTrials.gov Identifier: NCT06030700    
Other Study ID Numbers: PBRC 2023-045 B
First Posted: September 11, 2023    Key Record Dates
Last Update Posted: January 12, 2024
Last Verified: January 2024
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: Undecided
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 provided.

Layout table for additional information
Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No