Nutricity: A Pilot Study to Improve Parental Nutrition Literacy
1 other identifier
interventional
18
1 country
1
Brief Summary
The aim of this study is to engage parents and their young children (1-5 years of age) using the mobile intervention, Nutricity. Study goals are to increase parental nutrition literacy and improve eating habits of children.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Oct 2018
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
August 28, 2018
CompletedFirst Posted
Study publicly available on registry
September 17, 2018
CompletedStudy Start
First participant enrolled
October 15, 2018
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 12, 2019
CompletedStudy Completion
Last participant's last visit for all outcomes
August 12, 2019
CompletedSeptember 4, 2019
September 1, 2019
10 months
August 28, 2018
September 3, 2019
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Parental Nutrition Literacy
Measured by the Nutrition Literacy Assessment Instrument
12 weeks
Secondary Outcomes (1)
Child Diet Quality
12 weeks
Other Outcomes (1)
Skin Carotenoid Content
12 weeks
Study Arms (1)
Nutricity
EXPERIMENTALInterventions
Participants will use their smartphone or web-accessing device to access the Nutricity website to potentially increase nutrition literacy and set nutrition goals. Participants will have their own user name and password to access the site. Access to Nutricity will last approximately 3 months.
Eligibility Criteria
You may qualify if:
- Parents must be English speaking and must 1) Identify as primary food decision-maker for the home, 2) Have internet access at home and 3) Must have a device for accessing the internet. Smartphones, owned by \~75-92% of the target population, are adequate to satisfy the latter two criteria.
You may not qualify if:
- \) Overt cognitive or psychiatric illness, 2) Visual impairments that preclude reading survey instruments or using a tablet, 3) Child illness requiring a highly restrictive diet, such as renal disease, celiac disease, etc., 4) Planning to travel internationally during the study, 5) child is a foster child or ward of the state.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University of Kansas Medical Center
Kansas City, Kansas, 66160, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Heather D Gibbs, PhD, RD
University of Kansas Medical Center
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- PREVENTION
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
August 28, 2018
First Posted
September 17, 2018
Study Start
October 15, 2018
Primary Completion
August 12, 2019
Study Completion
August 12, 2019
Last Updated
September 4, 2019
Record last verified: 2019-09