Prevention & Promotion in the Treatment of Obesity

NCT ID: NCT02990494

Last Updated: 2018-08-15

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 96 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2016-12-31
• Study Completion Date: 2018-06-30

Brief Summary

Making healthy food choices requires sacrificing immediate pleasures of consuming high calorie foods in order to achieve long-term health goals. Two strategies to encourage such future thinking are 1) focusing on the long-term consequences of consuming unhealthy foods, and 2) focusing on the long-term benefits of avoiding these unhealthy foods. Two novel behavioral weight loss (BWL) interventions will be developed based on these strategies (PREVENT and PROMOTE) and compared to standard Internet-delivered BWL to test their feasibility and efficacy in changing food choice decision-making, reducing food cravings, and ultimate weight loss.

Detailed Description

Obesity is one of the most important public health issues today, contributing to many of the primary causes of morbidity and mortality in the United States. Still, treatment remains difficult and many people continually struggle to lose weight. Thus there is critical need for improvements in methods for treating obesity. One potential reason weight control is so difficult is the need to sacrifice immediate pleasures for long-term goals. This requires placing significant value on future outcomes, such as health.

One strategy for doing so is to focus on the potential benefits of avoiding unhealthy choices. Health messaging studies suggest that messages focused on promoting long-term benefits of healthier choices may be effective in encouraging initiation of, or positive attitudes toward, healthy behaviors, however, longer-term effects of these messages have not been studied in the context of obesity. By contrast, behavioral economic work on Prospect Theory suggests focusing on preventing future negative consequences may be superior, and the threat of weight gain is a more powerful motivator than the benefit of weight loss. Although prevention strategies have been successfully employed in smoking cessation and anti-smoking campaigns, they are not typically used in obesity treatment. In promising preliminary neuroimaging work, the investigators identified increases in brain regions involved in inhibitory control and decreases in cravings when using this PREVENT strategy.

The goal of this R03 is to test whether an intervention built upon the goal to PREVENT long-term consequences of weight gain versus an intervention built upon the goal to PROMOTE long-term benefits of weight loss is beneficial in altering valuation of health and taste in food choice decision-making, encouraging adherence, reducing food cravings and consumption, and ultimate weight loss, as compared to a standard behavioral weight loss program (BWL). A total of 90 overweight/obese men and women will be randomly assigned to either PREVENT, PROMOTE, or standard BWL. Each intervention will have one in-person training session wherein participants will learn key strategies of their assigned program, and the remaining 12 weekly lessons will be delivered via internet. Baseline and 3-month (post-treatment) assessments will include the food choice decision-making task featured in the parent K01 to measure valuation of health and taste, weight measurement, and measurement of food cravings and consumption. To address feasibility, adherence and engagement measures (i.e., lessons viewed, self-monitoring) will be collected during the internet program, and memory for lesson content will be assessed post-treatment. Individual difference measures will also be collected to provide preliminary data on factors that may influence success in each arm.

This project tests innovative approaches in the clinical treatment of obesity and will provide new insights into the potential role of prevention versus promotion strategies for weight loss.

Conditions

Obesity

Study Design

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

Study Groups

STANDARD

12-week Internet-delivered behavioral weight loss program

Group Type: ACTIVE_COMPARATOR

STANDARD

Intervention Type: BEHAVIORAL

Standard Internet-delivered behavioral weight loss

PREVENT

an enhanced 12-week Internet-delivered behavioral weight loss program focused on preventing future negative consequences

Group Type: EXPERIMENTAL

PREVENT

Intervention Type: BEHAVIORAL

enhanced standard Internet-delivered behavioral weight loss program

PROMOTE

an enhanced 12-week Internet-delivered behavioral weight loss program focused on promoting future benefits

Group Type: EXPERIMENTAL

PROMOTE

Intervention Type: BEHAVIORAL

enhanced standard Internet-delivered behavioral weight loss program

Interventions

STANDARD

Standard Internet-delivered behavioral weight loss

Intervention Type: BEHAVIORAL

PREVENT

enhanced standard Internet-delivered behavioral weight loss program

Intervention Type: BEHAVIORAL

PROMOTE

enhanced standard Internet-delivered behavioral weight loss program

Intervention Type: BEHAVIORAL

Other Intervention Names

Standard Internet-delivered behavioral weight loss; PREVENT Internet-delivered behavioral weight loss; PROMOTE Internet-delivered behavioral weight loss

Eligibility Criteria

Inclusion Criteria

• ages 25-60
• currently overweight or obese (BMI 25-45 kg/m2)

Exclusion Criteria

• lack of access to a computer and the Internet (needed once per week),
• weight loss medications
• neurological or psychiatric conditions including but not limited to schizophrenia, and bipolar disorder
• inability to attend assessments
• lack of interest in participating in a behavioral weight loss trial
• serious current physical disease for which physician supervision of diet and exercise prescription is needed
• physical problems that limit the ability to exercise
• participation in a weight loss program within the last 2 months
• intention to become pregnant in the next 3 months

• Minimum Eligible Age: 25 Years
• Maximum Eligible Age: 60 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

The Miriam Hospital

OTHER

Sponsor Role: lead

Responsible Party

Kathryn E. Demos

Assistant Professor (Research)

Responsibility Role: PRINCIPAL_INVESTIGATOR

Other Identifiers

1R03DK106405-01A1

Identifier Type: NIH

Identifier Source: org_study_id

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