Study Results
Outcome measurements, participant flow, baseline characteristics, and adverse events have been published for this study.
View full resultsBasic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
43 participants
OBSERVATIONAL
2021-02-10
2024-12-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
PortionSize Study 2 Free-Living Evaluation
NCT05166226
The PortionSize Smartphone App Pilot (PS Pilot)
NCT04494971
PortionSize Study 3: Assessment in Free-living Conditions
NCT05906160
Validity of an AI-based Program to Identify Foods and Estimate Food Portion Size
NCT05343585
Comparison of Medifast's 5 & 1 Plan to a Food-based Plan of Equal Calories
NCT01011491
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
The PortionSize™ app was designed by our laboratory to overcome the limitations outlined above, and to guide users to follow specific diets. PortionSize relies on users capturing images of their food selection and waste. Food intake data are immediately provided since the user relies on built in tools, including templates, to estimate portion size. However, despite promising early indications, the PortionSize app's validity has yet to be extensively tested. Determining the accuracy of PortionSize is vital before users can utilize the app to obtain immediate feedback about their food intake. We accordingly aim to test the validity of PortionSize in a controlled laboratory setting. We will also test the validity of the MyFitnessPal© app, which is similar to an electronic food record.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
CASE_CROSSOVER
PROSPECTIVE
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Body mass index (BMI) 18.5 - 50
* Ownership of an iPhone model 6s or later, which the participant is willing to use for the study
* Access to Apple ID, password, and email address and willing to use them in the course of the study
* Willing to use data and any accompanying charges as part of study participation
* Willing to be re-contacted for future research and/or follow-up
Exclusion Criteria
* Any condition or circumstance that could impede study completion
18 Years
70 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Pennington Biomedical Research Center
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Corby K. Martin
PBRC Professor, Director - Ingestive Behavior Laboratory
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
John W Apolzan, PhD
Role: PRINCIPAL_INVESTIGATOR
Pennington Biomedical Research Center
Corby K Martin, PhD
Role: PRINCIPAL_INVESTIGATOR
Pennington Biomedical Research Center
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Pennington Biomedical Research
Baton Rouge, Louisiana, United States
Countries
Review the countries where the study has at least one active or historical site.
References
Explore related publications, articles, or registry entries linked to this study.
Lozano CP, Neubig KE, Saha S, Broyles ST, Apolzan JW, Martin CK. Validity of the PortionSize application compared with that of MyFitnessPal for accurately estimating intake: a randomized crossover laboratory-based evaluation. Am J Clin Nutr. 2024 Aug;120(2):419-430. doi: 10.1016/j.ajcnut.2024.05.023. Epub 2024 May 31.
Provided Documents
Download supplemental materials such as informed consent forms, study protocols, or participant manuals.
Document Type: Study Protocol and Statistical Analysis Plan
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
PBRC 2019-062
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.