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Improving Dietary Behavior Through Tailored Messages

Improving Dietary Behavior Through Tailored Messages

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01864694
Enrollment
1224
Registered
2013-05-30
Start date
2008-11-30
Completion date
2011-07-31
Last updated
2013-05-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiovascular Disease

Keywords

behavioral research, diet, health information systems

Brief summary

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.

Detailed description

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.

Interventions

BEHAVIORALTLC-Diet

Participants receive diet intervention through an automated telephone system

BEHAVIORALWEB-Diet

Participants receive diet intervention through a web-based system

OTHERAssessment-only control

Assessment-only control

Sponsors

University of Rhode Island
CollaboratorOTHER
Boston Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Change in diet from baseline to 6 months, 6 months to 18 months, and baseline to 18 monthsBaseline, 6 months, and 18 monthsSelf-reported diet questionnaire to measure fat and fruits/vegetables

Secondary

MeasureTime frameDescription
Change in diet variables from baseline to 6 months, 6 months to 18 months, and baseline to 18 monthsBaseline, 6 months, and 18 monthsAdditional diet variables, such as total calories, trans fat, and carotenoids, as measured by self-reported food frequency questionnaire
Change in psychosocial variables from baseline to 6 months, 6 months to 18 months, and baseline to 18 monthsBaseline, 6 months, and 18 monthsAdditional theoretical variables, such as Stages of change, as measured by self-reported questionnaire

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026