Study Results
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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COMPLETED
10 participants
OBSERVATIONAL
2022-03-14
2023-12-31
Brief Summary
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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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Detailed Description
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Conditions
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Study Design
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CASE_CROSSOVER
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
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.
Eligibility Criteria
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Inclusion Criteria
* BMI ≥30 kg/m2
* Without a 4 year (BS/BA) college degree
* Owns a smart phone
* Able to read and speak English
Exclusion Criteria
18 Years
65 Years
ALL
Yes
Sponsors
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University of Minnesota
OTHER
Responsible Party
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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
Countries
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Other Identifiers
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MED-2021-30429
Identifier Type: -
Identifier Source: org_study_id
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