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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02920099
Other study ID # 13805
Secondary ID R03HD081730
Status Completed
Phase N/A
First received September 27, 2016
Last updated September 28, 2016
Start date June 2013
Est. completion date June 2016

Study information

Verified date September 2016
Source University of Kansas Medical Center
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial 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.


Recruitment information / eligibility

Status Completed
Enrollment 450
Est. completion date June 2016
Est. primary completion date June 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Able to speak and read English

- Have 1 or more of the following diseases: diabetes, hyperlipidemia, hypertension, and/or overweight/obesity

Exclusion Criteria:

- Visual acuity insufficient to read the testing instrument

- Cognitive impairment

- Weight > 500 pounds

Study Design

Observational Model: Case-Only, Time Perspective: Prospective


Related Conditions & MeSH terms


Intervention

Other:
Nutrition Literacy Assessment Instrument (NLAI)
Assessment tool which combines elements of different nutrition literacy tools.

Locations

Country Name City State
United States University of Kansas Medical Center Kansas City Kansas

Sponsors (2)

Lead Sponsor Collaborator
University of Kansas Medical Center Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary 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 No
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