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Behavioural Intervention

RFPM + SmartIntake App Validation for Caloric Intake (FoodPhone2 Trial)

N/A
Waitlist Available
Led By Corby K Martin, PhD
Research Sponsored by Pennington Biomedical Research Center
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be younger than 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 3 days
Awards & highlights

FoodPhone2 Trial Summary

This trial is testing how accurate a new method and app are for measuring how much energy (calories) someone eats.

Who is the study for?
Adolescents aged 12-18, with parental support for participants under 18, are eligible for this study. They must be willing to use the RFPM/SmartIntake app for about three days and respond to study staff when needed. The trial is open to boys and girls of any race.Check my eligibility
What is being tested?
The trial tests the accuracy of the Remote Food Photography Method (RFPM) and SmartIntake app in estimating adolescents' energy intake over several days against a scientific standard called doubly labeled water.See study design
What are the potential side effects?
Since this trial involves dietary assessment through an app rather than medication or medical procedures, there are no direct side effects from interventions like those seen with drugs or surgeries.

FoodPhone2 Trial Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~3 days
This trial's timeline: 3 weeks for screening, Varies for treatment, and 3 days for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Equivalence between energy intake (kcal/day) measured with the RFPM and DLW
Secondary outcome measures
Mean difference between the RFPM and DLW on kcal/day
Mean percentage error of RFPM relative to DLW

FoodPhone2 Trial Design

1Treatment groups
Experimental Treatment
Group I: Study sampleExperimental Treatment1 Intervention
Individuals who participate in this validation study

Find a Location

Who is running the clinical trial?

Pennington Biomedical Research CenterLead Sponsor
304 Previous Clinical Trials
181,407 Total Patients Enrolled
1 Trials studying Eating
24 Patients Enrolled for Eating
Corby K Martin, PhDPrincipal InvestigatorPennington Biomedical Research Center
9 Previous Clinical Trials
3,576 Total Patients Enrolled

Media Library

Tests of the validity of the RFPM and SmartIntake app (Behavioural Intervention) Clinical Trial Eligibility Overview. Trial Name: NCT04148560 — N/A
Eating Research Study Groups: Study sample
Eating Clinical Trial 2023: Tests of the validity of the RFPM and SmartIntake app Highlights & Side Effects. Trial Name: NCT04148560 — N/A
Tests of the validity of the RFPM and SmartIntake app (Behavioural Intervention) 2023 Treatment Timeline for Medical Study. Trial Name: NCT04148560 — N/A

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

What is the current recruitment quota for this clinical trial?

"Affirmative. The information available on clinicaltrials.gov attests that this research, which was initially posted October 1st 2020, is presently enrolling participants. A total of 24 trialists need to be admitted across a single medical facility."

Answered by AI

Are any new participants being enrolled in this research endeavor?

"As indicated on clinicaltrials.gov, this medical experiment is still looking to enrol patients; it was initially published on October 1st 2020 and recently updated on October 14th 2022."

Answered by AI

Is the cutoff age for this trial younger than 40 years old?

"This trial's admission requirements mandate that patients fall between the age range of 12 and 18 years old."

Answered by AI

Could I be eligible for inclusion in this investigation?

"This clinical research study is seeking 24 volunteers between the ages of 12 and 18 that are currently partaking in food consumption. Essential criteria for enrolment include parental permission (excepting those aged 18 years or above), consent to use the RFPM/SmartIntake app over a 3 day period plus an additional 1-2 days as a run-in, any gender identification and race, responsiveness to staff requests for supplementary information during application utilisation."

Answered by AI

Who else is applying?

What state do they live in?
Louisiana
How old are they?
18 - 65
What site did they apply to?
Pennington Biomedical Research Center
What portion of applicants met pre-screening criteria?
Did not meet criteria
Met criteria
Recent research and studies
clinicaltrials.govStudy
Free-living Validation of the RFPM in Adolescents
Corby K. Martin 2020. "Free-living Validation of the RFPM in Adolescents". ClinicalTrials.gov. https://clinicaltrials.gov/ct2/show/NCT04148560.
~6 spots leftby Apr 2025
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