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.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
Assessing User Satisfaction and Adherence to an Abbreviated Dietary Tracking App (MySnackTracker) Versus Full-intake Dietary Monitoring
At a glance
Conditions
Where it's being run
1 sites across 1 statesStudy leadership
- Karen M Basen-Engquist, MD · PRINCIPAL_INVESTIGATOR · M.D. Anderson Cancer Center
Who to contact
Opens a ready-to-send draft in your own email app — review before sending.
Do you actually qualify for this trial?
Add a private profile and we'll compare every criterion below against your situation — and tell you which ones are met, uncertain, or excluding.
Exclusion
What this trial measures
- 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