Project Health: Enhancing Effectiveness of an Obesity Prevention Program
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Project Health, Response and Attention Training, The Weight of the Nation.
- Who it may be relevant to
- Registry conditions: Overweight and Obesity, Eating Disorders. Basic parameters: 17 years — 20 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- United States
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
Enhancing Effectiveness of a Dissonance-Based Obesity Prevention Program: Randomized Controlled Trial
Overview
This 2-site effectiveness trial will test whether a brief dissonance-based obesity prevention program delivered in single sex groups combined with food response and attention training will produce significantly larger weight gain prevention effects than an educational video control condition. An effectiveness trial is important to test whether this program reduces risk for unhealthy weight gain when delivered by real world clinicians under ecologically valid conditions, which is an important step toward broad implementation. A secondary aim focuses on eating disorder symptom prevention effects. A sample of 17-20 year olds with weight concerns (N = 120) will be randomized to single sex Project Health groups with food response and attention training or an educational video control condition. Participants will complete assessments at baseline, posttest, and 6- and 12-month follow ups.
Detailed description
In the previous Project Health trial, the investigators found Project Health is most effective when implemented in single sex groups paired with food specific response and attention training. This project will evaluate the effectiveness of this version of the Project Health intervention compared to a video control condition and is an important step toward dissemination. A brief effective obesity prevention program that can be easily, inexpensively, and broadly implemented to late adolescents at risk for excess weight gain, as has been the case with another dissonance-based prevention program, could markedly reduce the prevalence of obesity and associated morbidity and mortality. The program may also have an important secondary benefit of preventing the onset of future eating symptoms and disorders. The study has 2 aims: (1) Test the hypothesis that Project Health implemented in single-sex groups and paired with food response inhibition and attention training produces significantly larger weight gain and overweight/obesity onset prevention effects than an educational video control condition (primary outcome). (2) Test the hypothesis that Project Health implemented in single-sex groups and paired with food response inhibition and attention training produces significantly larger eating disorder symptom prevention effects than an educational video control condition (secondary outcome).
Interventions
- Behavioral Project Health
A brief dissonance-based obesity prevention program delivered in six one-hour weekly sessions. - Behavioral Response and Attention Training
Individualized, computerized response and attention training consisting of five separate tasks designed to increase inhibitory control to reduce overeating. - Other The Weight of the Nation
This 2012 documentary discusses the facts and myths about obesity and the impacts of obesity on individuals and the health care system in the United States.
Primary outcome measures
- Body Fat [Time frame: baseline, posttest (approximately 8 weeks after baseline), 6-month follow-up (approximately 34 weeks after baseline), 12-month follow-up (approximately 60 weeks after baseline)]
Secondary outcome measures (1)
- Eating Disorder Symptoms [Time frame: baseline, posttest (approximately 8 weeks later), 6-month follow-up (approximately 34 weeks after baseline), 12-month follow-up (approximately 60 weeks after baseline)]
Eligibility criteria
Inclusion criteria
- Current at least moderate weight concerns (defined as a response of 4 or above on an 8 point scale ranging from none (0) to extreme (8))
- Self-reported room for improvement in diet and exercise habits (response of yes to "Do you believe there is room for improvement in your diet and exercise habits?" in the pre-screening questionnaire)
- BMI greater than or equal to 20 and less than or equal to 30
- Age between 17 and 20 years old
Exclusion criteria
- Current diagnosis of anorexia nervosa, bulimia nervosa or binge eating disorder
- Previous participation in a Project Health study
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Single blind
- Primary purpose
- Prevention
Study locations
United States · 2 centers
- Stanford University — Stanford
- Oregon Research Institute — Springfield
Publications
- Stice E, Rohde P, Gau JM, Shaw H. A Randomized Effectiveness Trial of a Dissonance-Based Dual Obesity and Eating Disorder Prevention Program. Diabetes Obes Metab. 2026 Jul;28(7):6034-6044. doi: 10.1111/dom.70775. Epub 2026 Apr 24. PMID 42028623
Identifiers
NCT: NCT06067763 · HD093598