An Environmental Intervention to Encourage Healthy Food Choices

Encouraging Healthy Food Choices With an Environmental Intervention in Military Dining Facilities

The primary objective of this study is to test effectiveness of an environmental intervention designed to encourage healthy food intake during meals. It is hypothesized that fruit, vegetable, whole grain, lean protein, and low-fat dairy consumption will increase during the intervention. It is also hypothesized that nutrition knowledge, attitudes, and behaviors will change as a result of the intervention. The findings from this study will provide insight into the applicability of this intervention in military dining facilities.

Study Overview

Detailed Description

Previous studies attempting to increase consumption of healthy foods in military dining facilities have had mixed results, and alternative approaches need to be considered. The present intervention was designed with the results of previous studies in mind, and as such, does not focus on labeling only healthy food choices. Instead, the present intervention aims to encourage consumption of nutritionally well-balanced meals using an environmental cue in military dining facilities.

Study Type

Interventional

Enrollment (Actual)

39

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Massachusetts
      • Natick, Massachusetts, United States, 01760
        • Natick Soldier Systems Center Dining Facility

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Military member or government civilian employee
  • Normally eat in military dining facility at least 1 day per week.

Exclusion Criteria:

  • N/A

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Non-Randomized
  • Interventional Model: Crossover Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Short Intervention
All participants will be measured for (1) baseline, (2) two-week environmental intervention: Healthy meal plates and trays, and (3) withdraw of intervention.
The healthy meal plates and trays provide guidance for how to construct a meal in the military dining facility.
Experimental: Long Intervention
All participants will be measured for (1) baseline, (2) four-week environmental intervention: Healthy meal plates and trays, and (3) withdraw of intervention.
The healthy meal plates and trays provide guidance for how to construct a meal in the military dining facility.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in dietary intake
Time Frame: Participants will be followed for 6-12 weeks
Dietary intake will be assessed at lunches eaten in military dining facilities using the food photography method. The change in dietary intake from baseline to intervention will be assessed.
Participants will be followed for 6-12 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in nutrition knowledge
Time Frame: Measured at beginning and end of the 6-12 week study.
Nutrition knowledge specific to the intervention will be assessed with an experimenter-developed questionnaire.
Measured at beginning and end of the 6-12 week study.
Change in nutrition attitudes and behaviors (composite)
Time Frame: Measured at the beginning and end of the 6-12 week study.
Nutrition attitudes and behaviors will be measured with a single composite experimenter-developed questionnaire.
Measured at the beginning and end of the 6-12 week study.

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Tracey J Smith, PhD, United States Army Research Institute of Environmental Medicine

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

August 1, 2013

Primary Completion (Actual)

July 1, 2014

Study Completion (Actual)

July 1, 2014

Study Registration Dates

First Submitted

July 31, 2013

First Submitted That Met QC Criteria

August 8, 2013

First Posted (Estimate)

August 13, 2013

Study Record Updates

Last Update Posted (Estimate)

May 4, 2016

Last Update Submitted That Met QC Criteria

May 3, 2016

Last Verified

May 1, 2016

More Information

Terms related to this study

Other Study ID Numbers

  • 13-14H

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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