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OpenTrials
Completed

NCT Number: NCT01864694

Improving Dietary Behavior Through Tailored Messages

The aim of this study is to compare a Web-based system and a computer telephone system to determine their effectiveness in improving diet behaviors compared to each other and a control group.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Boston Medical Center

Boston, Massachusetts, 02118, United States

About this study

The aim of this study is to compare a Web-based system (WEB-DIET) and a computer telephone system (TLC [Telephone Linked Communications]-DIET) for affecting dietary behavior change. These interventions will target the same dietary behaviors (consumption of fat and fruits and vegetables). The behavior change strategies and content will be derived from the same behavior change theory (the Transtheoretical Model [TTM]). A representative sample of ~1200 adults from a large urban area will be recruited through a list-assisted telephone list which will be bought by the University of Rhode Island so that subjects can be randomized into one of three groups: a Web-based system (WEB- DIET), a computer telephone system (TLC [Telephone Linked Communications]-DIET), or assessment only control. The study hypotheses, which will be evaluated both at the end of the 6-month intervention period and at the end of 18-month follow-up (post-baseline) observation period, are: 1. TLC-DIET> Control 2. WEB-DIET> Control 3. WEB-DIET> TLC-DIET.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • 18 years of age or older
  • Be at risk with regard to saturated fat
  • Have access to basic computer hardware and software
  • Use the Internet regularly (defined as 1 times per week) and with basic proficiency
  • Read and speak English at a fifth grade level
  • Have access to a telephone and be able to use it independently.

Exclusion criteria

  • Prescribed a diet that would conflict with a low saturated fat (e.g., a colectomy diet)
  • Have a serious medical, psychiatric, or cognitive disease that would interfere with participation (e.g., cancer undergoing chemotherapy, psychotic disorder, Alzheimer's disease, etc.)
  • If the individual does not use the Internet at least once a week

Treatment and study plan

TLC-Diet

Behavioral

Participants receive diet intervention through an automated telephone system

WEB-Diet

Behavioral

Participants receive diet intervention through a web-based system

Assessment-only control

Other

Assessment-only control

Primary outcomes

  1. Change in diet from baseline to 6 months, 6 months to 18 months, and baseline to 18 months

    Time frame: Baseline, 6 months, and 18 months

    Self-reported diet questionnaire to measure fat and fruits/vegetables

Secondary outcomes

  1. Change in psychosocial variables from baseline to 6 months, 6 months to 18 months, and baseline to 18 months

    Time frame: Baseline, 6 months, and 18 months

    Additional theoretical variables, such as Stages of change, as measured by self-reported questionnaire

  2. Change in diet variables from baseline to 6 months, 6 months to 18 months, and baseline to 18 months

    Time frame: Baseline, 6 months, and 18 months

    Additional diet variables, such as total calories, trans fat, and carotenoids, as measured by self-reported food frequency questionnaire

Sponsors and collaborators

Lead sponsor

Boston Medical Center

Other

Collaborators

  • University of Rhode Island

Registry information

Important dates

Study start
2008
Primary completion
2011
Study completion
2011
First posted
May 30, 2013
Registry last updated
May 30, 2013

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.

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