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Free-living Validation of the RFPM in Adolescents (FoodPhone2)

Pennington Biomedical Research Center logo

Pennington Biomedical Research Center

Status

Active, not recruiting

Conditions

Energy Intake
Dietary Assessment
Food Photography
Food Intake

Treatments

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

Study type

Interventional

Funder types

Other

Identifiers

NCT04148560
PBRC 2019-053

Details and patient eligibility

About

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.

Full 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.

Enrollment

29 patients

Sex

All

Ages

12 to 18 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • 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

Exclusion criteria

  • 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 design

Primary purpose

Other

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

29 participants in 1 patient group

Study sample
Other group
Description:
Individuals who participate in this validation study
Treatment:
Other: Tests of the validity of the RFPM and SmartIntake app.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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