Adaptation and Validation of a Nutrition Literacy Assessment Instrument
2 other identifiers
observational
450
1 country
1
Brief Summary
The purpose of this study is to develop a tool to help researchers better understand what diet information people know and what skills they use to make diet choices.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jun 2013
Typical duration for all trials
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
Study Start
First participant enrolled
June 1, 2013
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 1, 2016
CompletedStudy Completion
Last participant's last visit for all outcomes
June 1, 2016
CompletedFirst Submitted
Initial submission to the registry
September 27, 2016
CompletedFirst Posted
Study publicly available on registry
September 30, 2016
CompletedSeptember 30, 2016
September 1, 2016
3 years
September 27, 2016
September 28, 2016
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Change in Nutrition Literacy Assessment Instrument (NLAI) responses
Participants will complete the NLAI two times over the course of one month. Responses will help shape adaptions to the tool for use in a primary care population.
1 month
Study Arms (1)
Nutrition Literacy
Participants will be asked to completed the Nutrition Literacy Assessment Instrument (NLAI).
Interventions
Assessment tool which combines elements of different nutrition literacy tools.
Eligibility Criteria
University of Kansas Medical Center (KUMC) students
You may qualify if:
- Able to speak and read English
- Have 1 or more of the following diseases: diabetes, hyperlipidemia, hypertension, and/or overweight/obesity
You may not qualify if:
- Visual acuity insufficient to read the testing instrument
- Cognitive impairment
- Weight \> 500 pounds
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 Gibbs, PhD, RD, LD
University of Kansas Medical Center
Study Design
- Study Type
- observational
- Observational Model
- CASE ONLY
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
September 27, 2016
First Posted
September 30, 2016
Study Start
June 1, 2013
Primary Completion
June 1, 2016
Study Completion
June 1, 2016
Last Updated
September 30, 2016
Record last verified: 2016-09