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SMARTer Weight Loss Management (SMARTer)

Primary Purpose

Obesity

Status
Not yet recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Adaptive SMARTer intervention (SMARTer)
Diabetes Prevention Program Participants (DPP)
Sponsored by
Northwestern University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Obesity

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Over 18 years old BMI of ≥25, weight <396 lbs Must own a Smartphone, and be willing to install the SMARTer app Participants must also plan to reside in the Chicagoland area for the duration of their participation (i.e., 12 months) 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

Sites / Locations

  • Northwestern University

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

No Intervention

Arm Label

Adaptive SMARTer intervention (

Diabetes Prevention Program Participants (DPP)

Assessments-Only (Control)

Arm Description

Smartphone application, diet and activity goals, online lessons, brief remote sessions with a Health Promotionist. Will have physical measures taken at baseline, 3 months, 6 months, 9 months, and 12 months.

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.

Resources educating on leading a healthier lifestyle, including information on wellness and physical activity. Will have physical measures taken or extracted from the medical record at baseline, 3 months, 6 months, 9 months, and 12 months.

Outcomes

Primary Outcome Measures

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

Secondary Outcome Measures

Cost
Costs of SMARTer versus DPP versus Control implementation. We will utilize a micro-costing approach to capture all costs associated with the implementation of the treatment arms.

Full Information

First Posted
May 8, 2023
Last Updated
May 8, 2023
Sponsor
Northwestern University
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1. Study Identification

Unique Protocol Identification Number
NCT05861973
Brief Title
SMARTer Weight Loss Management
Acronym
SMARTer
Official Title
SMARTer Weight Loss Management
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
January 2024 (Anticipated)
Primary Completion Date
January 2027 (Anticipated)
Study Completion Date
April 2027 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Northwestern University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

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 usual care assessment-only (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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obesity

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
This is a randomized control trial with 3 parallel intervention arms. One arm will be the SMARTer active treatment group, one the active DPP treatment group, and the other an assessments-only control group. Assessors will be blinded to study condition, and intervention will be behavioral.
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
492 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Adaptive SMARTer intervention (
Arm Type
Experimental
Arm Description
Smartphone application, diet and activity goals, online lessons, brief remote sessions with a Health Promotionist. Will have physical measures taken at baseline, 3 months, 6 months, 9 months, and 12 months.
Arm Title
Diabetes Prevention Program Participants (DPP)
Arm Type
Experimental
Arm Description
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.
Arm Title
Assessments-Only (Control)
Arm Type
No Intervention
Arm Description
Resources educating on leading a healthier lifestyle, including information on wellness and physical activity. Will have physical measures taken or extracted from the medical record at baseline, 3 months, 6 months, 9 months, and 12 months.
Intervention Type
Behavioral
Intervention Name(s)
Adaptive SMARTer intervention (SMARTer)
Intervention Description
Participants will receive calorie, fat, and physical activity goals, a Smartphone application for self-monitoring their diet, activity and weight, online educational readings, and brief bi-weekly remote health sessions with a Health Promotionist. They will also be loaned a Fitbit tracking device and a wireless bluetooth scale for 6 months.
Intervention Type
Behavioral
Intervention Name(s)
Diabetes Prevention Program Participants (DPP)
Intervention Description
In accordance with the Center for Disease Control curriculum, participants will receive a participant log for tracking physical activity, food intake, and weight, a paper participant guide with worksheets, logs, and psycho-educational materials, and 16 hour long remote sessions with a Health Promotionist.
Primary Outcome Measure Information:
Title
Weight
Description
Participant change in weight, in pounds, from baseline to 6-months.
Time Frame
Baseline to 6-Months
Secondary Outcome Measure Information:
Title
Cost
Description
Costs of SMARTer versus DPP versus Control implementation. We will utilize a micro-costing approach to capture all costs associated with the implementation of the treatment arms.
Time Frame
12 Months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
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 Participants must also plan to reside in the Chicagoland area for the duration of their participation (i.e., 12 months) 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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Laura Scanlan, MS
Phone
312-503-1395
Email
laura.scanlan@northwestern.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Bonnie Spring, PhD
Organizational Affiliation
Northwestern University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Angela Pfammatter, PhD
Organizational Affiliation
University of Tennesse-Knoxville
Official's Role
Principal Investigator
Facility Information:
Facility Name
Northwestern University
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60611
Country
United States
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Laura Scanlan, MS
Phone
312-503-1395
Email
laura.scanlan@northwestern.edu
First Name & Middle Initial & Last Name & Degree
Bonnie Spring, PhD

12. IPD Sharing Statement

Plan to Share IPD
No

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SMARTer Weight Loss Management

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