Clinical trial

Supporting Decisions on Lifestyle Change

Invitation only · Not applicable · 1 countries · Registry ID NCT06206954

Invitation onlyNot applicableInterventional

What this study is about

This study will test the effects of a brief, individually tailored intervention aiming to increase initiation of comprehensive behavioral weight loss treatment on weight.

A promising-looking record is not the same as confirmed eligibility. The study team must review the full criteria and current recruitment status.

Basic eligibility

Age18 Years to Not listed
SexAll
Healthy volunteersNot accepted
ConditionObesity

Full registry criteria

Inclusion Criteria: * Age 18 or older * Body Mass Index (BMI) ≥ 30 kg/m2 based on self-report body weight and height, or BMI ≥ 27-29.9 kg/m2 with a weight related comorbidity of hypertension, type 2 diabetes, pre-diabetes, dyslipidemia, or obstructive sleep apnea, gastroesophageal reflux disease, or coronary artery disease. * Self-report weight ≤ 375 lbs (the maximum weight that BodyTrace scales can accurately detect is 397 lbs, thus 375 lbs provides a buffer to allow detection of at least 20 lbs weight gain). * Has a desire to weigh less * Has valid email address in Electronic Health Record * Has an appointment scheduled with enrolled PCP about 21-28 days after electronic data pull * Speaks and reads English * Has either WiFi internet access at home or a phone or tablet with a data plan. Exclusion criteria * Currently enrolled in evidence-based comprehensive weight loss treatment * Pregnant or planning to become pregnant in the next 6 months * Currently breastfeeding (or pumping breastmilk) more than 3 times per day. * Currently undergoing treatment for cancer * Had cardiovascular event in the past 60 days * Severe depression symptoms on PHQ-8 (total score ≥20) * Inpatient psychiatric treatment in the past 6 months * Eating disorder in past 5 years * Congestive heart failure resulting in recent (past 6 months) hospitalization or contributing to difficulty breathing or difficulty doing daily activities. * Dementia diagnosis * Bariatric surgery in the past year or currently undergoing evaluation for bariatric surgery * Currently taking doctor-prescribed medication for weight loss * Inability to stand on body weight scale independently * Impaired hearing * Unable to read content on websites without assistance

Treatments and study arms

MyHealthPath Tool

Behavioral

Tailored, brief online tool to help patients learn about weight treatment options

MyHealthPath Guide

Behavioral

Informational material to help patients learn about weight treatment options

Primary outcomes

Proportion initiating treatmentWithin 2 months of PCP appointment date

Attend at least one intervention session of comprehensive behavioral weight loss intervention. Documented by interventionist/program.

Study locations

1 locations were listed when this page was built. The first 40 are shown.

University of Florida🇺🇸 Gainesville, Florida, United States