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OpenTrials
Completed

NCT Number: NCT05228171

Mobile Food Record on Recall Effects

Human dietary habits remain challenging to measure. Even the "gold-standard" interviewer-administered 24 hour dietary recall has established underreporting issues especially in high-risk populations, such as patients with obesity. Performance of precision nutrition research requires state of the art tools to capture individual dietary patterns. Given the widespread availability of smart phones, mobile-phone based food records present a prime opportunity to capture "in the field" dietary intake. Mobile food records, however, are not yet widely used in nutrition research. Several reasons exist. First, the mobile food record needs to be validated relative to the "gold standard" of dietary intake, the 24-hour dietary recall. Second, many available mobile food records are commercially based, with caveats about data availability and meeting research-quality data security practices (HIPAA compliance).

In response, this study includes using a freely available, research-focused, HIPAA compliant, mobile food record (mCC: my Circadian Clock app) actively used in research studies (including our own ongoing work) to test the hypothesis that a mobile food record can expand capture of dietary intake. The proposed aims include the following: Using a randomized, cross-over design, evaluation of augmenting interviewer-administered 24-hour dietary recalls by a mobile food record (Augmented Recall) results in less energy intake underreporting than a standard (un-augmented) interviewer administered 24-hour dietary recall (Standard Recall).

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Key information

Conditions

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Observational

Primary location

University of Minnesota

Minneapolis, Minnesota, 55455, United States

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adults between 18-65 years old
  • BMI ≥30 kg/m2
  • Without a 4 year (BS/BA) college degree
  • Owns a smart phone
  • Able to read and speak English

Exclusion criteria

  • Pregnant or lactating women

Treatment and study plan

mCC app

Behavioral

Interviewer use of the mCC app during the 24-hour dietary recall interview.

Primary outcomes

  1. Caloric intake

    Time frame: 60 days from intervention

    Compare caloric intake assessed by the augmented recall relative to the standardized recall

Secondary outcomes

  1. Energy intake

    Time frame: 24 hours following food intake

    Comparison of the energy intake calculated from the 24 hour interviewer administered dietary recall which is augmented by concurrent use and review of a mobile food record (Augmented Recall) vs the energy intake calculated from standard interviewer administered 24-hour dietary recall (Standard Recall)

Sponsors and collaborators

Lead sponsor

University of Minnesota

Other

Registry information

Official study title

Use of a Mobile Food Record, Enhanced by a Novel Artificial Intelligence-Based Informatics Framework to Expand Capture of Dietary Intake

Important dates

Study start
2022
Primary completion
2022
Study completion
2023
First posted
Feb 8, 2022
Registry last updated
Feb 2, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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