Assessing User Satisfaction and Adherence to an Abbreviated Dietary Tracking App (MySnackTracker) Versus Full-intake Dietary Monitoring
2 other identifiers
interventional
90
1 country
1
Brief Summary
To learn if a method of abbreviated food tracking (called MySnackTracker) is a reasonable alternative to traditional full-intake food tracking and to compare the adherence to and acceptability of each method.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Apr 2025
Longer than P75 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
April 2, 2025
CompletedStudy Start
First participant enrolled
April 8, 2025
CompletedFirst Posted
Study publicly available on registry
April 9, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 1, 2028
ExpectedStudy Completion
Last participant's last visit for all outcomes
May 1, 2030
November 10, 2025
November 1, 2025
3.1 years
April 2, 2025
November 6, 2025
Conditions
Outcome Measures
Primary Outcomes (1)
Safety and adverse events
Incidence of Adverse Events, Graded According to National Cancer Institute Common Terminology Criteria for Adverse Events
Through study completion; an average of 1 year
Study Arms (2)
Group 2: Fitbit
EXPERIMENTALParticipants in Group 2, will use the Fitbit food logging app to track their dietary intake. Participants will be asked to log all food and drink intake.
Group 1: MySnackTracker
EXPERIMENTALParticipants in Group 1 will use MySnackTracker to track their dietary intake. Participants will be asked to log only high-calorie, low-nutrient food and drinks, or snacks" (for example, cookies, chips and dip, and alcohol). A full list of these foods and drinks is provided in the app.
Interventions
Eligibility Criteria
You may not qualify if:
- An participant who meets any of the following criteria will be excluded from participation in this study:
- 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
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
MD Anderson Cancer Center
Houston, Texas, 77030, United States
Related Links
Study Officials
- PRINCIPAL INVESTIGATOR
Karen M Basen-Engquist, MD
M.D. Anderson Cancer Center
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- HEALTH SERVICES RESEARCH
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
April 2, 2025
First Posted
April 9, 2025
Study Start
April 8, 2025
Primary Completion (Estimated)
May 1, 2028
Study Completion (Estimated)
May 1, 2030
Last Updated
November 10, 2025
Record last verified: 2025-11