Comparing MySnackTracker App to Full Dietary Monitoring

This study is looking at two ways to track what you eat: using a special app called MySnackTracker, which focuses on high-energy, low-nutrient foods, or tracking everything you eat. Researchers want to see if MySnackTracker is easier to stick with and if people like it more than traditional full-intake tracking. You would wear a Fitbit and use either the MySnackTracker app or a full-intake dietary monitoring method. To join, you need to be at least 18 years old, have internet access, an email, a smartphone, and have participated in certain previous DFI studies. The main goal is to check for any safety issues during the study, which is expected to last about one year. The current recruitment status is unclear.

Study design
This is an interventional study comparing two different dietary tracking methods, with a planned enrollment of 90 participants. It is not specified if it is randomized or blinded.
What's involved
You would wear a Fitbit and use a dietary tracking app. The study duration is approximately one year.
Compensation
Not stated in the trial record.
Follow-up
Safety and adverse events will be measured through study completion, which is an average of one year.

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NCT06919471

Assessing User Satisfaction and Adherence to an Abbreviated Dietary Tracking App (MySnackTracker) Versus Full-intake Dietary Monitoring

Recruiting
NAAges 18+InterventionalHealth services
M.D. Anderson Cancer Center
~90 participants
Updated 2026-05-29 on ClinicalTrials.gov
What's tested:FitbitMySnackTracker App

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Safety and adverse events
Measured over Through study completion; an average of 1 year
Dietary Monitoring
1 sites across 1 states
Texas1
  • Karen M Basen-Engquist, MD · PRINCIPAL_INVESTIGATOR · M.D. Anderson Cancer Center

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Eligibility criteria

Exclusion

Prisoners
Anyone currently under 18 years of age
Cognitively impaired participants
Pregnant women (assessed by self-report)
BMI less than 28 or greater than 40
Self-reported previous or planned bariatric surgery
Self-reported current or planned use of a GLP-1 agonist medication
Self-reported current or planned participation in another weight loss intervention
Cancer participants receiving active treatment
Anyone currently unable to participate in the research for the duration of the study
No current motivation to lose weight
  • Safety and adverse eventsThrough study completion; an average of 1 year

    Incidence of Adverse Events, Graded According to National Cancer Institute Common Terminology Criteria for Adverse Events