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Online Obesity Treatment in Primary Care (Rhode Island, USA)

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Lifespan

Status

Unknown

Conditions

Overweight and Obesity

Treatments

Behavioral: Control Intervention for Weight Loss Maintenance and Weight Gain Prevention
Behavioral: Refresher Courses for Weight Loss Maintenance and Weight Gain Prevention
Behavioral: Training to Motivate and Support Patients' Weight Loss
Behavioral: Online Behavioral Weight Loss Intervention
Behavioral: Training to Identify Eligible Patients and Direct them to Online Obesity Treatment Program
Behavioral: Monthly Lessons and Feedback Intervention for Weight Loss Maintenance and Weight Gain Prevention

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT03488212
R18DK114715 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

Behavioral obesity treatment produces clinically significant weight loss; for the greatest impact, it should be made available in the primary care setting where it can reach the many patients with overweight/obesity. The investigators developed a 3-month automated online behavioral weight loss program, Rx Weight Loss (RxWL), and showed that it produces clinically significant weight losses among primary care patients. The investigators' early efforts at pragmatic implementation of RxWL have been promising, and have shed light on challenges associated with implementation, and the need to study longer-term effectiveness. The investigators will therefore conduct a pragmatic study to improve the implementation and effectiveness of this behavioral obesity intervention delivered in routine and representative healthcare settings. The investigators are partnering with the Rhode Island Primary Care Physicians Corporation (RIPCPC), a large primary care network of 58 practices with 100 physicians and 16 nurse care managers. Using the framework for Effectiveness-Implementation Hybrid Designs, the investigators will simultaneously target effectiveness and implementation to maximize the public health impact of the research. Half of the 16 nurse care managers, and the practices they serve, will be randomized to either Basic Implementation (alerts generated using the electronic medical record [EMR] to direct eligible patients to RxWL), or to the Enhanced Implementation (alerts, clinician skills training to motivate and support weight loss, clinician dashboard with reports on patient progress and tools to facilitate patient engagement and behavior change). The investigators will test the hypothesis that the Enhanced Implementation will increase the proportion of patients directed to, enrolling, and completing the weight loss program. Because maintenance of weight loss is a critical problem, this project will also involve randomization of 600 patients with overweight/obesity and type 2 diabetes, hypertension, and/or hypercholesterolemia to the 3 month RxWL intervention followed by one of three maintenance conditions: (a) Control- 9 monthly online education sessions; (b) Monthly Lessons and Feedback- 9 monthly online video lessons teaching self-regulation with automated feedback on the self-monitoring record; (c) Refresher Campaigns- 9 monthly on-line video sessions, teaching self-regulation and providing two 4-week courses with novel strategies and behavioral challenges to improve long-term outcomes. The investigators will test the hypothesis that 12-month weight losses are better with Refresher Campaigns than Monthly Lessons and Feedback, and both are better than Control. Secondary outcomes include changes in weight, CVD risk factors, and medication use over a full 24 months. The project is significant and innovative because: it uses an empirically validated approach to obesity treatment that is integrated into the primary care setting, leveraging existing staff and EMR capabilities; it has a dual focus on improving effectiveness and implementation; it has a pragmatic design in partnership with a large primary care network that treats a diverse patient population; and it has potential to it provides a scalable, sustainable approach that can serve as a model for broader dissemination of obesity treatment intervention.

Enrollment

600 estimated patients

Sex

All

Ages

18 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Body mass index (BMI) between 25-45 kg/meters-squared
  • one or more cardiovascular risk factor (type 2 diabetes, hypercholesterolemia, or hypertension)

Exclusion criteria

  • currently in another active weight loss program
  • taking weight loss medication
  • currently pregnant, lactating
  • <6 months post-partum
  • plan to become pregnant during the next 12 months
  • a medical condition that would affect the safety of participating in unsupervised physical activity
  • inability to walk 2 blocks without stopping

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

600 participants in 5 patient groups

Basic Implementation Intervention
Active Comparator group
Treatment:
Behavioral: Training to Identify Eligible Patients and Direct them to Online Obesity Treatment Program
Enhanced Implementation Intervention
Experimental group
Treatment:
Behavioral: Training to Motivate and Support Patients' Weight Loss
Behavioral: Training to Identify Eligible Patients and Direct them to Online Obesity Treatment Program
Online Treatment; Control Maintenance Intervention
Active Comparator group
Treatment:
Behavioral: Control Intervention for Weight Loss Maintenance and Weight Gain Prevention
Behavioral: Online Behavioral Weight Loss Intervention
Online Treatment; Monthly Lessons & Feedback for Maintenance
Experimental group
Treatment:
Behavioral: Online Behavioral Weight Loss Intervention
Behavioral: Monthly Lessons and Feedback Intervention for Weight Loss Maintenance and Weight Gain Prevention
Online Treatment; Refresher Courses for Maintenance
Experimental group
Treatment:
Behavioral: Refresher Courses for Weight Loss Maintenance and Weight Gain Prevention
Behavioral: Online Behavioral Weight Loss Intervention

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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