Validation of a Food Frequency Questionnaire: VioScreen
NCT ID: NCT05762718
Last Updated: 2024-10-01
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
27 participants
OBSERVATIONAL
2022-12-16
2024-04-16
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
CROSS_SECTIONAL
Eligibility Criteria
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Inclusion Criteria
* Pregnant women up to 26 weeks' gestation
* Women assigned female sex at birth who are not pregnant
Exclusion Criteria
* Pregnant women more than 26 weeks' gestation at the time of enrollment
* Women who are experiencing limited or reduced food intake related to nausea will not be approached for recruitment and are considered ineligible
* Women who are unwilling to participate in the study due to time commitment or other reasons
* Women whose capacity for study compliance is diminished due to conditions such as active untreated substance use disorder, untreated/uncontrolled schizophrenia, bipolar disorder, active psychosis will not be approached for recruitment and are considered ineligible
18 Years
40 Years
FEMALE
Yes
Sponsors
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University of Colorado, Denver
OTHER
Responsible Party
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Principal Investigators
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Carina Venter, PhD
Role: PRINCIPAL_INVESTIGATOR
University of Colorado, Denver
Locations
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Children's Hospital Colorado
Aurora, Colorado, United States
Denver Health
Denver, Colorado, United States
Countries
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Other Identifiers
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22-0904
Identifier Type: -
Identifier Source: org_study_id
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