N/A
Completed N=45
PortionSize Study 2 Free-Living Evaluation
Dietary Habits
Source: ClinicalTrials.gov NCT05166226 ↗
Enrolled (actual)
45
Serious AEs
0.0%
Results posted
Dec 2025
Primary outcomePrimary: Energy (Kilocalorie or kcal) Intake — 2128.8; 2120.0 kcal/day
Summary
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.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Energy (Kilocalorie or kcal) Intake |
2128.8; 2120.0 | — |
Eligibility Criteria
Inclusion Criteria
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
Exclusion Criteria
- 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
Data sourced from ClinicalTrials.gov (NCT05166226). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.