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NCT05228171 · ClinicalTrials.gov registry record
Mobile Food Record on Recall Effects
A clinical trial, sponsored by University of Minnesota.
- Completed
- Registry status
- 10
- Enrollment target
NCT05228171 is a clinical trial that has completed, run by University of Minnesota. The registered enrollment target is 10 participants.
The verdict
NCT05228171 has completed, sponsored by University of Minnesota.
- COMPLETED
- Registry status
- 10 participants
- Enrollment target
Study Summary
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).
Interventions
- BEHAVIORAL mCC app
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 10 participants |
| Start Date | 2022-03-14 |
| Est. Completion | 2023-12-31 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05228171
The ClinicalTrials.gov registry entry for NCT05228171 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 10 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Minnesota, which has 966 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which mCC app is the first listed.
NCT05228171 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT05228171 about?
NCT05228171 is a clinical study titled "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...
What is the current status of trial NCT05228171?
This trial is currently completed. The enrollment target is 10 participants. The study started on 2022-03-14. Estimated completion is 2023-12-31.
What interventions are being tested in trial NCT05228171?
The interventions under investigation include: mCC app (BEHAVIORAL).
Who is sponsoring clinical trial NCT05228171?
This trial is sponsored by University of Minnesota, which has 966 total clinical trials registered on ClinicalTrials.gov.
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