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OpenTrials
Completed

NCT Number: NCT00415870

mDiet - Ecological Momentary Intervention of Diet Via Mobile Technology

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.

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Key information

Age range

25 year–55 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

UCSD Professional Suites

La Jolla, California, 92037, United States

About this study

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.

Who can participate

Healthy volunteers accepted: No

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

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.

Treatment and study plan

Printed Material

Behavioral

Printed Material

Weekly Weighing

Behavioral

Weekly Weighing

Cell phone will serve as a self monitoring device

Behavioral

Cell phone will serve as a self monitoring device

Text Message

Device

Text Message

Diet Goals via Cell Phone

Behavioral

Diet Goals via Cell Phone

Food Monitoring

Behavioral

Food Monitoring

Primary outcomes

  1. Mean Weight (kg)

    Time frame: 4 months

Secondary outcomes

  1. Program Satisfaction

    Time frame: 4 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.

  2. Compliance With Food Monitoring Activities

    Time frame: 4 months

Sponsors and collaborators

Lead sponsor

University of California, San Diego

Other

Registry information

Official study title

Ecological Momentary Intervention of Diet Via Mobile Technology

Important dates

Study start
2007
Primary completion
2009
Study completion
2009
First posted
Dec 25, 2006
Registry last updated
Apr 30, 2019

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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