- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05963906
Food Survey, Curbside, Remote APPs SCFI (FoodSCRAPPSCFI)
December 5, 2024 updated by: John Apolzan, Pennington Biomedical Research Center
An Innovative, Accessible, and Flexible Approach for Household Food Waste Measurement - SCFI
The proposed research will create accurate and standardized household food waste measurement technologies that foster serial and longitudinal assessments as well as confident and convenient one-time measurement.
The investigators propose the SCFI field study where participants simultaneously deploy 3 measurement approaches (1) retrospective surveys (2) curbside audits, and (3) the FoodImage smartphone app.
Study Overview
Status
Completed
Conditions
Study Type
Observational
Enrollment (Actual)
57
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
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Baton Rouge, Louisiana, United States, 70808
- Pennington Biomedical Research Center
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Ohio
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Columbus, Ohio, United States, 43210
- Ohio State University
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-
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
Accepts Healthy Volunteers
Yes
Sampling Method
Probability Sample
Study Population
Participants will be from the greater Columbus, OH and Baton Rouge, LA areas.
Description
Inclusion Criteria:
- Male or Female, age 18-64 years
- Willing and able to store household food waste for curbside pickup by a third-party waste pickup company
- Internet or Wi-Fi availability to complete online surveys
- 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:
- Not willing to adhere to study procedures and study visit timelines
- 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 |
|---|
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SCFI
SCFI participants will complete a survey once per week for three consecutive weeks.
They will participate in training for the FoodImage app and deploy it the last two weeks of their study period.
During these last two weeks, these participants will also have waste collected on designated days by a waste pickup contractor.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Household Food Waste
Time Frame: 1 week
|
Weight
|
1 week
|
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Household Food Waste
Time Frame: 1 week
|
Energy (kcal)
|
1 week
|
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)
October 10, 2023
Primary Completion (Actual)
November 19, 2024
Study Completion (Actual)
November 19, 2024
Study Registration Dates
First Submitted
July 14, 2023
First Submitted That Met QC Criteria
July 19, 2023
First Posted (Actual)
July 27, 2023
Study Record Updates
Last Update Posted (Estimated)
December 10, 2024
Last Update Submitted That Met QC Criteria
December 5, 2024
Last Verified
December 1, 2024
More Information
Terms related to this study
Other Study ID Numbers
- PBRC 2023-007 B
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
IPD Plan Description
All IPD that underlie results in a publication after a DTA with the institution.
Please provide a research question.
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- ICF
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.
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