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mDiet - Ecological Momentary Intervention of Diet Via Mobile Technology

Not Applicable
Completed
Conditions
Overweight
Registration Number
NCT00415870
Lead Sponsor
University of California, San Diego
Brief Summary

This is a NCI funded study which will develop and evaluate a cell phone application (mDIET) that can be used as an assessment and intervention tool to improve dietary behaviors and thus reduce weight in overweight and moderately obese (BMI 25-34.9) men and women ages 25-55.

Detailed Description

This research will develop a technologically advanced system for monitoring and intervening on diet behaviors (e.g., food intake, weight). Interventions aimed at dietary change are missing a comparable, portable tool. Mobile technologies can help fill this gap by providing portable connectivity to expert systems that create specific tailored diet goals based on participant profiles. The expert system can 'push' intervention messages throughout the day during critical point-of-decision moments to aid in decision making among users. The portable device can 'pull' information through prompts and easy-to-use recording. This ecological momentary assessment + ecological momentary intervention format may further encourage healthy behaviors by prompting at critical decision points to improve dietary behaviors.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
65
Inclusion Criteria
  • Participants will be included if they:

    • Are age 25-55
    • Are overweight or moderately obese
    • Are with a BMI between 25.0-34.9 (as defined by the NIH report on Obesity (NIH 1998)
    • Are able to read (completion of at least the 6th grade) and speak English
    • Provide consent
    • Do not intend to become pregnant or move out of the county for the duration of the intervention (16 weeks).
  • Participants will also be required to have a cell phone that is capable of supporting the mDIET application.

  • Participants may be otherwise healthy or have one or more risk factors for CVD, including uncomplicated Type 2 diabetes but will not be enrolled if they have diagnosed CVD.

Exclusion Criteria

Participants will be excluded from the study if they have any of the following conditions:

  • An eating disorder
  • Are currently pregnant
  • Have a strict dietary regimen prescribed by their doctor that will not allow them to comply with intervention guidelines related to dietary changes.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Mean Weight (kg)4 months
Secondary Outcome Measures
NameTimeMethod
Program Satisfaction4 months

Participants reported a 2 if they liked the program, 1 if they felt neutral about the program, and 0 if they did not like program. Higher scores reflect greater satisfaction.

Compliance With Food Monitoring Activities4 months

Trial Locations

Locations (1)

UCSD Professional Suites

🇺🇸

La Jolla, California, United States

UCSD Professional Suites
🇺🇸La Jolla, California, United States

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