跳至主要内容
临床试验/NCT06919471
NCT06919471招募中不适用

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

M.D. Anderson Cancer Center1 个研究点 分布在 1 个国家目标入组 90 人开始时间: 2025年4月8日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
90
试验地点
1
主要终点
Safety and adverse events

研究概览

简要总结

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.

详细描述

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Single Group
主要目的
Health Services Research
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •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.

排除标准

  • •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

研究组 & 干预措施

Group 2: Fitbit

Experimental

Participants 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.

干预措施: Fitbit (Other)

Group 1: MySnackTracker

Experimental

Participants 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.

干预措施: MySnackTracker App (Other)

结局指标

主要结局

Safety and adverse events

时间窗: Through study completion; an average of 1 year

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

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

Loading locations...

相似试验