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Dietary AssessmentFoodPhone2NCT04148560

Free-living Validation of the RFPM in Adolescents

A study testing Tests of the validity of the RFPM and SmartIntake app. in people with Dietary Assessment and Energy Intake, run by Pennington Biomedical Research Center at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The primary aim of this small study is to test the validity of the Remote Food Photography Method and an updated SmartIntake app in a sample of adolescents. The investigators will test the validity (accuracy) of the method/app at estimating energy intake in free-living conditions over approximately three days compared… Read more about this study

Who is it for?
Ages 12 to 18 yearsHealthy volunteers can take part
Conditions the study is for
Dietary Assessment, Energy Intake, Food Intake
What is being tested?
Tests of the validity of the RFPM and SmartIntake app.
Could I receive a placebo?
No, everyone receives an active treatment
How many people
29 participants
Where
1 siteUnited States
Study dates
1 Oct 2020to 31 Dec 2025
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 12 to 18 years
  • All sexes
  • Healthy volunteers accepted
  • Child, Adult

Who may be able to join

  • boy or girl of any race
  • age between 12 and 18 years
  • willingness to use the RFPM/SmartIntake app for 3 days, in addition to a 1-2 day run-in period
  • willingness to be responsive to study staff when prompted for additional information when using the RFPM/SmartIntake app
  • parental support of the project, except for 18-year-olds

Who cannot join

  • Individuals may not qualify for this study based on other eligibility criteria not listed. The study coordinator determine this on a case-by-case basis

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Pennington Biomedical Research Center

    Baton Rouge, Louisiana, 70808

Other trials in United States

About this study

Official title: Validity of the Remote Food Photography Method to Measure Food Intake in Adolescents in Free-living Conditions

The primary aim of this small study is to test the validity of the Remote Food Photography Method and an updated SmartIntake app in a sample of adolescents. The investigators will test the validity (accuracy) of the method/app at estimating energy intake in free-living conditions over approximately three days compared to doubly labeled water. This is a small study that has low statistical power, but will provide important data nonetheless and inform future research.

Read the detailed description

Energy intake (EI) is an important predictor of weight gain (1) and accurate methods to measure children's and adolescent's EI are needed. Self-report methods (e.g., 24-hour recall and food records) have their strengths and are frequently used to measure children's EI. Nonetheless, they also have significant limitations, including participant and caregiver burden and lack of near real-time data.

Our group developed the Remote Food Photography Method (RFPM) to measure the EI of adults in near real-time and the validity data in adults are exceptional; the RFPM underestimates EI in laboratory settings by less than 6% and in free-living conditions by less than 7% compared to weighed foods and by less than 4% compared to doubly labeled water (DLW) over 6 days. At the same time, participant burden is drastically reduced compared to self-report methods, as participants are only required to capture images of their food selection and plate waste with a smartphone app and send these images to the laboratory for analysis. This validation study aims to assess the accuracy of the RFPM and SmartIntake app in a sample of adolescents in free-living conditions.

Being tested
Tests of the validity of the RFPM and SmartIntake app.

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Tests of the validity of the RFPM and SmartIntake app.Other

    Participants who enroll will be trained in using the RFPM/SmartIntake app and a food record and will complete the Food Intake Assessment Preference Survey. They will also use both methods to estimate intake during a simulated lab-based meal (they will not eat during this simulated meal). They will be dosed with DLW at this visit and will use the RFPM for the subsequent 1-2 days to get accustomed to using the method, with the following three days comprising the data collection period.

Study groups in NCT04148560
Study groupRoleWhat they receive
Study sampleOtherIndividuals who participate in this validation study
Receives: Other: Tests of the validity of the RFPM and SmartIntake app.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Equivalence between energy intake (kcal/day) measured with the RFPM and DLW

    Energy intake is measured by the RFPM and DLW in kcal per day over 3 days. We will use the mean of the 3 days in the analyses. Two one-sided paired t-tests (α = 0.05 for each) will be performed in this pilot with equivalence bounds at 2% increments between 8% and 34% to determine equivalence in kcal estimates between RFPM and DLW.

    Measured: 3 days

Secondary outcomes (2)
  1. Mean difference between the RFPM and DLW on kcal/day

    RFPM - DLW (kcal), with each method measuring energy intake over three days, and the mean of the three days for each method being included in the calculations and analyses.

    Measured: 3 days

  2. Mean percentage error of RFPM relative to DLW

    MPE = (RFPM - DLW) / DLW × 100

    Measured: 3 days

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted1 Nov 2019
  2. Study start1 Oct 2020
  3. Primary completion17 Apr 2023
  4. Study completion31 Dec 2025

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Other
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
29 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04148560
Sponsor's protocol ID
PBRC 2019-053
Acronym
FoodPhone2
Status last verified
Apr 2026
First submitted
28 Oct 2019
Last updated
5 May 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: Access to individual de-identified data is possible via Pennington Biomedical Research Center's Data Sharing policy.

Publications

  • Hochsmann C, Diktas HE, Myers CA, Dorling JL, Rood JC, Greenway F, Champagne CM, Apolzan JW, Martin CK. The validity of measuring energy and nutrient intake with the Remote Food Photography Method (RFPM) in adolescents. Am J Clin Nutr. 2026 Jul 25;124(3):101452. doi: 10.1016/j.ajcnut.2026.101452. Online ahead of print.

    PubMed 42501948

Questions about this trial

What is this clinical trial studying?

A study testing Tests of the validity of the RFPM and SmartIntake app. in people with Dietary Assessment and Energy Intake, run by Pennington Biomedical Research Center at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 5 May 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Equivalence between energy intake (kcal/day) measured with the RFPM and DLW (time frame: 3 days). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT04148560, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 5 May 2026.

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