NCT05972824

Brief Summary

Participants will perform the FoodImage app in the lab. A survey will be provided after the study visit. Also the bag of combined waste will be given to a hired contractor who will sort and weigh the waste, thus creating a second estimate of waste and its key components using standard industry practices (i.e. curbside).

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
24

participants targeted

Target at below P25 for all trials

Timeline
Completed

Started Dec 2023

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

July 19, 2023

Completed
14 days until next milestone

First Posted

Study publicly available on registry

August 2, 2023

Completed
4 months until next milestone

Study Start

First participant enrolled

December 13, 2023

Completed
11 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 21, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

November 21, 2024

Completed
Last Updated

December 6, 2024

Status Verified

December 1, 2024

Enrollment Period

11 months

First QC Date

July 19, 2023

Last Update Submit

December 5, 2024

Conditions

Outcome Measures

Primary Outcomes (1)

  • Food Waste Weight

    Weight (g)

    Study Visit ~ 1 day

Secondary Outcomes (1)

  • Food Waste Energy

    Study Visit ~1 day

Eligibility Criteria

Age18 Years - 62 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)
Sampling MethodProbability Sample
Study Population

Healthy participants from the greater Baton Rouge, LA area.

You may qualify if:

  • Male or female, age 18-62 years
  • Has 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 participation. Willing to complete all study procedures and adhere to study timelines.

You may not qualify if:

  • Refusal or unable to use an iPhone for study related purposes
  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Pennington Biomedical Research Center

Baton Rouge, Louisiana, 70808, United States

Location

Study Officials

  • John W Apolzan, PhD

    Pennington Biomedical Research Center

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
CASE ONLY
Time Perspective
OTHER
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Associate Professor-Research

Study Record Dates

First Submitted

July 19, 2023

First Posted

August 2, 2023

Study Start

December 13, 2023

Primary Completion

November 21, 2024

Study Completion

November 21, 2024

Last Updated

December 6, 2024

Record last verified: 2024-12

Data Sharing

IPD Sharing
Will share

All IPD that underlie results in a publication after a DTA with the institution. A research question should be included.

Shared Documents
STUDY PROTOCOL, ICF

Locations