PortionSize Study 2 Free-Living Evaluation
Completed
Conditions studied: Dietary Habits
In brief
The objective is to test the accuracy of the PortionSize™ app and the MyFitnessPal© app at measuring energy and nutrient intake in free-living conditions. Participants will use PortionSize™ and MyFitnessPal apps in separate periods to test the accuracy of the respective apps.
Key facts
- Study ID
- NCT05166226
- Run by
- Pennington Biomedical Research Center
- People needed
- 45
- Starts
- 2022-01-10
- Expected to finish
- 2026-03-31
- Last updated by the study team
- 2026-05-13
Who can join
Age: 18 and older, up to 62. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Male or female, age 18-62 years
- Body mass index (BMI) 18.5-50 kg/m2
- Subjects who are capable of giving informed consent and complying with all study procedures/requirements.
- 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 during the study
- Willing to use data and any accompanying charges as part of study participation
- Willing to complete all study procedures and adhere to study visit timelines
- Willing to be re-contacted for future research and/or follow-up
You may not qualify if…
- Active cancer diagnosis (excluding some melanomas)
- Have been 6-month weight unstable (gain/loss >10 lbs in last 6 months)
- Undergoing weight loss treatment
- PBRC employee, as previous reviewers argued that they are not representative of the community
- Women who are currently pregnant or breastfeeding (self-reported)
- Diagnosed with an uncontrolled thyroid disorder (controlled = 3 months of medication)
- Have had or plan to have weight loss surgery (gastric band removal may be allowed at PI discretion)
- Allergic to or unwilling to eat study foods provided (exceptions made at the discretion of the PI)
- Consume >28 alcoholic beverages per week
- Anyone severely immunocompromised
- Any condition or circumstance that in the judgement of the PI could interfere with study participation
Where it is running
- Pennington Biomedical Research Center — Baton Rouge, Louisiana, United States
Full record on ClinicalTrials.gov
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