The purpose of this study is to develop and test an adaptive, individually tailored intervention to prevent weight regain in people who have intentionally lost weight. The main questions it aims to answer are: * Is an adaptive intervention with tailored re-engagement support feasible for individuals following intentional weight loss? * Does this intervention prevent weight regain after intentional weight loss? Participants will: * Complete a baseline assessment of body measurements * Complete surveys on dietary intake, mental health, and physical activity Participants will also engage in a 26-week program, which involves: * Receive regular educational texts/emails * Fill out weekly online survey check-ins * Weigh themselves at least weekly on a scale provided by the study * Some participants may receive health coaching during portions of the study. * Assessments will be repeated for all participants at the end of the intervention period.
Age range
18 Years – 65 Years
Sex
ALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Feasibility - Participant Retention
Timeframe: From enrollment to the end of the 26-week monitoring period
Feasibility - Participant Adherence
Timeframe: From enrollment to the end of the 26-week monitoring period
Efficacy - Participant Weight
Timeframe: From enrollment to the end of the 26-week monitoring period
Efficacy - Participant Dietary Intake
Timeframe: From enrollment to the end of the 26-week monitoring period
Efficacy - Eating Self-Efficacy in High-Risk Situations
Timeframe: From enrollment to the end of the 26-week monitoring period
Efficacy - Eating Behavior Patterns
Timeframe: From enrollment to the end of the 26-week monitoring period
Efficacy - Sleep/Rest Duration
Timeframe: From enrollment to the end of the 26-week monitoring period
Efficacy - Daily Step Count
Timeframe: From enrollment to the end of the 26-week monitoring period
Efficacy - Sedentary Behavior (Sitting/Lying Time)
Timeframe: From enrollment to the end of the 26-week monitoring period
Efficacy - Standing Time
Timeframe: From enrollment to the end of the 26-week monitoring period