Optimization of Dietary Adherence in a Mobile Weight Loss Intervention

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorUNC Lineberger Comprehensive Cancer Center

About this trial

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.

Eligibility criteria

Qualifiers

BMI 25-50 kg/m2 at baseline

Own a smartphone with an active data and text messaging plan

English-speaking and writing

Willing to be randomized to any of the additional treatment components

Disqualifiers

Lost 5% or more of body weight (and kept it off) in the last 3 months

Past diagnosis of or receiving treatment for a clinically diagnosed eating disorder (anorexia nervosa or bulimia nervosa)

Current symptoms of alcohol or substance dependence

Currently pregnant, pregnant within the past 6 months, currently breastfeeding, or planning to become pregnant within the next 6 months

Trial design

Treatments tested in this trial

  • Core
  • Switch to Simplified Diet Monitoring
  • Goal Autonomy/Planning
  • Just-in-time (JIT) Messaging
  • Coach Sessions

Treatment groups

580 Participants
are divided into 17 treatment groups

17

Treatment groups

See each treatment group below.

Sponsors and collaborators

UNC Lineberger Comprehensive Cancer Center

Lead sponsor

National Heart, Lung, and Blood Institute (NHLBI)

Collaborator