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Completed

NCT Number: NCT00468156

The Fruit and Vegetable Study

The main aim of this study is to determine if persons can increase fruit and vegetable intakes if they make a specific plan to do so.

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Key information

Conditions

Age range

40 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Ypsilanti Family Health Center

Ypsilanti, Michigan, 48197, United States

About this study

The conduct of cancer prevention trials through community settings and/or national networks of clinical sites requires the development of appropriate interventions. One promising behavioral strategy that is very simple to administer is that of the formulation of implementation intentions. The premise of this intervention is that once persons formulate a plan of action, automatic behavior follows. Use of this intervention in primary care is an innovative approach to eliciting preventive behaviors with minimal staff time. The goal in this study will be to increase fruit and vegetable consumption by 2 servings/day without a change in overall energy intakes by decreasing consumption of a less nutritious food. Substitution of foods is critical for prevention of weight gain. This feasibility study aims conduct a randomized, controlled clinical trial to test whether formulation of implementation intentions, either alone or with telephone support, can increase fruit and vegetable consumption without an increase in overall energy intakes. Recruitment success in a family medicine clinic in Ypsilanti Michigan will be documented with emphasis on the extent of minority participation. Dietary assessment will be the main outcome variable. Other assessments will include demographics, self-assessment of behaviors targeted by the intervention and levels of carotenoids in plasma. We will enroll 105 subjects to retain 28/arm, and power is good to detect small differences in fruit and vegetable intakes among the three study arms. This will generate useful data for the design of larger dietary intervention trials that are cost-effective and which will utilize multiple clinical sites to optimize enrollment.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age 40 and older
  • Give informed consent
  • In general good health
  • Less than 5.5 servings/day of fruits and vegetables

Exclusion criteria

  • On medically prescribed diets that the study would not be consistent with
  • Evidence of eating disorders
  • Health problems that affect energy needs (eg. broken leg can interfere with normal activities and affect energy needs).

Treatment and study plan

written materials only

Behavioral

related to fruit/vegetable servings/day

Other names: control

Written Materials

Behavioral

related to fruit/vegetable servings/day

Other names: asked to form implementation intentions

telephone support

Behavioral

related to fruit/vegetable servings/day

Other names: written plus telephone

Primary outcomes

  1. Document enrollment success at a primary care clinic

    Time frame: 8 months

Secondary outcomes

  1. Determine change in fruit and vegetable consumption

    Time frame: 3 months

Sponsors and collaborators

Lead sponsor

University of Michigan

Other

Registry information

Official study title

Implementation Intentions for Improving Fruit and Vegetable Intakes

Important dates

Study start
2006
Primary completion
2007
Study completion
2008
First posted
May 2, 2007
Registry last updated
Dec 20, 2012

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.