Dietary Monitoring
Conditions
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.
Detailed description
Primary Objectives The goal of the study is to compare the adherence and acceptability of tracking only high-energy low-nutrient value foods to standard full intake monitoring of diet. We predict that use of the high-energy, low-nutrient-density food tracking app will result in greater adherence to self-monitoring and greater satisfaction with monitoring in comparison to the full intake tracking. Secondary Objectives Assess the efficacy of the snack tracking app versus standard self-monitoring as measured by changes in the following measures between baseline and follow up; percentage weight change, weight loss self-efficacy scores, food logging self-efficacy scores, GODIN leisure time activity questionnaire scores, Vioscreen tool responses for stages of change for fats and fruit/vegetable intake, daily fruit consumption, daily vegetable consumption, servings of sweets per day, Healthy Eating Index (HEI) Score for calories from solid fats, alcohols, added sugars, HEI empty calories, total drinks of alcohol per day, calories from alcoholic beverages per day, added sugars by available carbohydrates, added sugars by total grams of sugar, calorie intake, carbohydrate intake, fat intake, saturated fatty acid intake, and total sugar intake.
Interventions
OTHERFitbit
Wear it on wrist
OTHERMySnackTracker App
App to track your dietary intake
Sponsors
M.D. Anderson Cancer Center
Study design
Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
Eligibility Criteria In order to be eligible to participate in this study, an participants must meet all of the following criteria: * Provision of signed and dated informed consent form * Access to internet connection, email address, and smartphone able to download the intervention app * Current or previous participation in one of the following DFI cohorts: PA17-0584 (MERIT Study), Project CHURCH, High Risk Breast Cohort, Mexican-American Cohort, and rural cancer survivors from the Mind Your BEAT study * Demonstrated ability to read and understand English. The study app is currently only available in English.
Exclusion criteria
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
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Safety and adverse events | Through study completion; an average of 1 year | Incidence of Adverse Events, Graded According to National Cancer Institute Common Terminology Criteria for Adverse Events |
Countries
United States
Contacts
CONTACTKaren M Basen-Engquist, MD
PRINCIPAL_INVESTIGATORKaren M Basen-Engquist, MD
M.D. Anderson Cancer Center
Outcome results
None listed