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Clinical Trials/NCT06206954
NCT06206954
Enrolling By Invitation
Not Applicable

Increasing Initiation of Evidence-based Weight Loss Treatment

University of Florida1 site in 1 country864 target enrollmentJanuary 24, 2024
ConditionsObesity

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Obesity
Sponsor
University of Florida
Enrollment
864
Locations
1
Primary Endpoint
Proportion initiating treatment
Status
Enrolling By Invitation
Last Updated
10 months ago

Overview

Brief Summary

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

Registry
clinicaltrials.gov
Start Date
January 24, 2024
End Date
July 30, 2028
Last Updated
10 months ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility 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

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Proportion initiating treatment

Time Frame: Within 2 months of PCP appointment date

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

Secondary Outcomes

  • Number of treatment sessions attended(6 months)
  • Proportion achieving 5% weight loss(6 months)
  • Percent weight loss(6 months)
  • Proportion discussing weight-related topic with PCP(at completion of PCP visit (occuring up to 4 weeks after enrollment))

Study Sites (1)

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