Energy Balancing Modeling and Mobile Technology to Support e-Weight Loss

NCT ID: NCT02857595

Last Updated: 2016-08-05

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: NA
• Total Enrollment: 30 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2016-07-31

Brief Summary

Behavioral lifestyle treatment for obesity produces clinically significant weight loss and corresponding improvements in disease risk and severity when delivered via in-person group and/or individual treatment sessions. Online versions have been developed in order to reduce costs. These programs typically include weekly weight loss lessons and tailored feedback on patients' weight loss progress. However, online programs often produce suboptimal outcomes compared to programs delivered in-person due to insufficient adherence to prescribed behavioral strategies, and a lack of objective methods for behavioral self-monitoring to support adherence. One approach to monitoring and improving adherence involves tracking patients' weight loss progress on a personalized nomogram (i.e., graph). The nomogram is based on a dynamic energy balance equation and depicts the expected weight loss over time if the participant is adherent to a prescribed goal for caloric intake and physical activity. A complementary approach to measuring and intervening on adherence involves the use of mobile technology to monitor eating behavior. The Bite Counter is a wrist-worn device similar to a wristwatch that measures the timing, frequency, rate, and duration of eating events by monitoring the "wrist roll" motion that occurs when food is brought to the mouth. By using mathematical models to "calibrate" the Bite Counter to the weight loss nomogram, it may be possible to identify the optimal number of bites that any given patient should take each day in order to facilitate weight loss. The purpose of the proposed study is to conduct a small randomized controlled trial to test the feasibility, acceptability, and preliminary efficacy of adding weight loss nomograms and the Bite Counter to an established online weight loss program. A sample of 30 participants with overweight/obesity will be randomly assigned in equal proportions to one of three 12-week weight loss programs: (a) online behavioral weight loss treatment alone (OBWL), (b) online behavioral weight loss treatment plus the provision of weight loss nomograms with weekly feedback tailored to the nomogram (OBWL+N), or (c) online behavioral weight loss treatment plus the provision of weight loss nomograms with weekly feedback tailored to the nomogram and provision of a Bite Counter that can be used to alert participants when they are approaching their maximum number of prescribed bites per day (OBWL+N&BC).

Conditions

Overweight; Obesity

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: DOUBLE

Study Groups

Online Weight Loss Program

Group Type: ACTIVE_COMPARATOR

Online Behavioral Weight Loss program

Intervention Type: BEHAVIORAL

Online Weight Loss Program + Nomogram

Group Type: EXPERIMENTAL

Online Behavioral Weight Loss program

Intervention Type: BEHAVIORAL

Weight Loss Nomogram

Intervention Type: BEHAVIORAL

Online Weight Loss Program + Nomogram + Bite Counter

Group Type: EXPERIMENTAL

Online Behavioral Weight Loss program

Intervention Type: BEHAVIORAL

Weight Loss Nomogram

Intervention Type: BEHAVIORAL

Bite Counter

Intervention Type: BEHAVIORAL

Interventions

Online Behavioral Weight Loss program

Intervention Type: BEHAVIORAL

Weight Loss Nomogram

Intervention Type: BEHAVIORAL

Bite Counter

Intervention Type: BEHAVIORAL

Eligibility Criteria

Inclusion Criteria

• Body mass index (BMI) between 27 and 45 kg/m^2

Exclusion Criteria

• Self-report of health problems that make weight loss or unsupervised exercise unsafe or unreasonable
• A heart condition, chest pain during periods of activity or rest, or loss of consciousness on the Physical Activity Readiness Questionnaire
• Currently pregnant or intend to become pregnant in the next 6 months
• Planning to move outside of the geographic region within the next 6 months
• Self-report any cognitive or physical limitations that preclude use of a personal computer
• Participation in a study conducted at the research center in the past 2 years
• Use of a commercial weight loss program within the last 6 months
• Self-report a history of clinically diagnosed eating disorder excluding Binge Eating Disorder
• Previous surgical procedure for weight loss
• Current use of weight loss medication
• Treatment of cancer within the last 6 months

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 70 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

The Miriam Hospital

OTHER

Sponsor Role: lead

Responsible Party

John Graham Thomas

Associate Professor (Research)

Responsibility Role: PRINCIPAL_INVESTIGATOR

Locations

Miriam Hospital Weight Control and Diabetes Resarch Center

Providence, Rhode Island, United States

Site Status: RECRUITING

Countries

United States

Central Contacts

Graham Thomas, PhD

Role: CONTACT

jthomas4@lifespan.org

4017938154

Facility Contacts

Graham Thomas, PhD

Role: primary

jthomas4@lifespan.org

401-793-8154

References

Goldstein CM, Goldstein SP, Thomas DM, Hoover A, Bond DS, Thomas JG. The Behavioral Intervention with Technology for E-Weight Loss Study (BITES): Incorporating Energy Balance Models and the Bite Counter into an Online Behavioral Weight Loss Program. J Technol Behav Sci. 2021 Jun;6(2):406-418. doi: 10.1007/s41347-020-00181-4. Epub 2020 Nov 27.

Reference Type: DERIVED

PMID: 35356149 (View on PubMed)

Other Identifiers

212715 45CFR 46.110(4)(7)

Identifier Type: -

Identifier Source: org_study_id