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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT02259023
Other study ID # DFS2014
Secondary ID
Status Withdrawn
Phase N/A
First received September 29, 2014
Last updated October 24, 2017
Start date February 2014
Est. completion date February 2015

Study information

Verified date October 2017
Source University of Minnesota - Clinical and Translational Science Institute
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Purpose:

The objective of this study is to determine the effect different sources and forms of discretionary foods have on stress perception in healthy adults in a free living, real world setting.

Rationale:

The rationale for conducting this study is to test the effects of sugar-sweetened beverages and grain-based desserts have on perceived health and stress perception, since the evidence for this topic is limited.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date February 2015
Est. primary completion date February 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria:

- Adults who consume sugar sweetened beverages and grain based desserts and candy on a regular basis

- Free from major illnesses or chronic disease

- Willing to consume amount of beverages and food provided to supplement usual dietary habits during each period

Exclusion Criteria:

- Recently lost a significant amount or looking to lose weight

- Recently begun a new diet or exercise regimen

- Pregnant or nursing women

- Report restrained eater or having less than 51% control over food preparation

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Liquid: Sugar sweetened beverage consumption
Sugar sweetened beverage consumption
Solid: Grain based desserts and candy consumption
Grain based desserts and candy consumption

Locations

Country Name City State
United States University of Minnesota West Bank Office Building Minneapolis Minnesota

Sponsors (1)

Lead Sponsor Collaborator
University of Minnesota - Clinical and Translational Science Institute

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Stress Perception A questionnaire adapted from the SF-12 will be used to measure stress perception. 12 weeks
Secondary Body Weight A digital scale will be used to measure body weight. 12 weeks