Optimization of Dietary Adherence in a Mobile Weight Loss Intervention
NCT07582536 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 580
Last updated 2026-05-15
Summary
The goal of this study is to test multiple individual treatment components added to a 6-month standard mobile behavioral weight loss program that are intended to help participants follow dietary recommendations and meet their dietary goals more often. The four components to be studied include switching dietary tracking methods, receiving access to a goal planning tool, receiving additional personalized text messages, and receiving three sessions with a health coach. The study will identify the best combination of these additional treatments for improving total number of weeks in the program that participants meet their dietary goals.
Conditions
- Overweight and/or Obesity
Interventions
- BEHAVIORAL
-
Coach Sessions
Receive 3 brief telephone or video coach sessions (20-30 minutes) every other week following randomization.
- BEHAVIORAL
-
Core
Behavioral weight loss core includes daily self-monitoring (tracking) of dietary intake, physical activity, and weight; personalized daily goals for dietary intake and physical activity; weekly behavioral lessons in the study app; weekly tailored feedback on goal progress and weight change; 5-6 text messages per week.
- BEHAVIORAL
-
Switch to Simplified Diet Monitoring
Switch from standard detailed calorie tracking to a simplified diet self-monitoring approach in which participants track red foods using a color-coded traffic light system.
- BEHAVIORAL
-
Goal Autonomy/Planning
A weekly goal planning tool that allows participants to adjust their dietary goals and make a specific plan for the week.
- BEHAVIORAL
-
Just-in-time (JIT) Messaging
Increased frequency of text messages (1-2 per day), highly personalized based on past and current dietary adherence and weight change.
Sponsors & Collaborators
-
National Heart, Lung, and Blood Institute (NHLBI)
collaborator NIH -
UNC Lineberger Comprehensive Cancer Center
lead OTHER
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- DOUBLE
- Model
- FACTORIAL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2027-03-31
- Primary Completion
- 2029-09-30
- Completion
- 2029-10-31
Countries
- United States
Study Locations
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