Mobile Food Record on Recall Effects

NCT ID: NCT05228171

Last Updated: 2024-02-02

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

10 participants

Study Classification

OBSERVATIONAL

Study Start Date

2022-03-14

Study Completion Date

2023-12-31

Brief Summary

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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).

Detailed Description

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Conditions

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Healthy

Study Design

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Observational Model Type

CASE_CROSSOVER

Study Time Perspective

PROSPECTIVE

Study Groups

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Standard Recall

Standard interviewer-administered 24-hour dietary recall.

No interventions assigned to this group

Augmented Recall

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

mCC app

Intervention Type BEHAVIORAL

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

Interventions

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mCC app

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

Intervention Type BEHAVIORAL

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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University of Minnesota

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Lisa Chow, MD

Role: PRINCIPAL_INVESTIGATOR

UMN

Locations

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University of Minnesota

Minneapolis, Minnesota, United States

Site Status

Countries

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United States

Other Identifiers

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MED-2021-30429

Identifier Type: -

Identifier Source: org_study_id

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