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Clinical Trials/NCT05861973
NCT05861973
Recruiting
Not Applicable

SMARTer Weight Loss Management

Florida State University1 site in 1 country492 target enrollmentJune 25, 2024

Overview

Phase
Not Applicable
Intervention
Adaptive SMARTer intervention (SMARTer)
Conditions
Obesity
Sponsor
Florida State University
Enrollment
492
Locations
1
Primary Endpoint
Weight
Status
Recruiting
Last Updated
17 days ago

Overview

Brief Summary

The SMARTer trial will be a three-arm, randomized controlled non-inferiority trial that compares the optimized, adaptive SMARTer intervention, fixed DPP, and Self-Guided (Control). The trial will address whether a scalable, stepped-care intervention can stand up to gold-standard DPP by achieving comparable weight loss at a lower cost. Alongside evaluation of clinical non-inferiority, a comprehensive economic evaluation will inform relative affordability. Cost information is important to inform treatment policy and change standard of care, but is sorely lacking for behavioral interventions. The SMARTer intervention reduces costs by initially offering minimal intervention to all and stepping up to offer more costly treatment components only to non-responders who fail to attain the target weight loss. A rigorous economic evaluation planned and designed alongside the SMARTer trial will provide an accurate, robust head-to-head comparison of costs, cost-effectiveness, and projected lifetime health care costs between the three arms.

Detailed Description

The proposed study seeks to test the hypothesis that SMARTer is non-inferior to DPP in its effect on 6-month weight loss. During the 24-week active intervention phase, participants will be randomized to one of three first-line treatments: 1) the adaptive SMARTer intervention, 2) fixed DPP, or 3) usual care assessment-only (control). Participants will be assessed at 3-month, 6-month, 9-month, and 12-month timepoints to evaluate overall weight loss, and to explore whether SMARTer is cost-effective compared to DPP or standard care.

Registry
clinicaltrials.gov
Start Date
June 25, 2024
End Date
October 31, 2027
Last Updated
17 days ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Bonnie Spring

Krafft Professor of Behavioral Sciences and Social Medicine and Director of Florida Blue Center for Rural Health Research & Policy

Florida State University

Eligibility Criteria

Inclusion Criteria

  • Over 18 years old
  • BMI of ≥25, weight \<396 lbs
  • Must own a Smartphone, and be willing to install the SMARTer app
  • Not enrolled in a formal weight loss program

Exclusion Criteria

  • Cerebrovascular accident or myocardial infarction within six months of enrollment
  • Diabetes treated with insulin
  • Pregnancy, lactation or intended pregnancy
  • Active suicidal ideation
  • Anorexia or bulimia
  • Requiring an assistive device for mobility
  • Taking weight loss medications, such as GLP-1 agonists

Arms & Interventions

Adaptive SMARTer intervention (SMARTer)

Smartphone application, diet and activity goals, online lessons, brief remote sessions with a Health Promotionist. Data from a wifi scale will be monitored. Individuals losing less than .5 lb per week will be stepped up to also be given meal replacement products. Will have physical measures taken at baseline, 3 months, 6 months, 9 months, and 12 months.

Intervention: Adaptive SMARTer intervention (SMARTer)

Diabetes Prevention Program (DPP)

Fixed intervention using participant program manual, diet and activity logs, hour long remote sessions with a Health Promotionist. Will have physical measures taken at baseline, 3 months, 6 months, 9 months, and 12 months.

Intervention: Diabetes Prevention Program (DPP)

Self-Guided Treatment (Self-Guided)

Provides paper and internet resources tailored to geographic area, educating on leading a healthier lifestyle, including information on wellness and physical activity. Will have physical measures taken at baseline, 3 months, 6 months, 9 months, and 12 months.

Intervention: Self-Guided Treatment (Self-Guided)

Outcomes

Primary Outcomes

Weight

Time Frame: Baseline to 6-Months

Participant change in weight, in pounds, from baseline to 6-months.

Weight - percent change

Time Frame: Baseline to 6-months

Participant percent change in weight (kg) from baseline to 6-months.

Weight - difference in kg

Time Frame: Baseline to 6-months

Participant change in weight (kg) from baseline to 6-months.

Secondary Outcomes

  • Cost(12 Months)
  • Cost(12-months)

Study Sites (1)

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