Understanding dietary lapses in obesity treatment
Using Multimodal Real-Time Assessment to Phenotype Dietary Non-Adherence
This study is trying to understand why people sometimes struggle to stick to their diet while getting help for obesity, by tracking their habits and feelings over 18 months.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 150 (estimated) |
| Ages | 18 Years to 70 Years |
| Sex | All |
| Sponsor | The Miriam Hospital Academic / other |
| Locations | 1 site (Providence, Rhode Island) |
| Trial ID | NCT05562427 on ClinicalTrials.gov |
What this trial studies
This project aims to investigate dietary lapses, which are instances of failing to adhere to dietary goals during behavioral obesity treatment. By utilizing multimodal real-time assessments, including wearable sensors and a smartphone-based platform, the study will identify different phenotypes of dietary lapses among participants. Over 18 months, 150 individuals will receive online behavioral obesity treatment, allowing researchers to analyze the behavioral, psychosocial, and contextual factors that contribute to these lapses. The findings will inform future personalized interventions to enhance dietary adherence.
Who should consider this trial
Good fit: Ideal candidates for this study are adults aged 18-70 with a body mass index (BMI) between 25 and 50 kg/m².
Not a fit: Patients with health issues contraindicating weight loss, those currently pregnant or breastfeeding, or individuals with a history of clinically diagnosed eating disorders (excluding Binge Eating Disorder) may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to more effective personalized interventions for individuals struggling with obesity by reducing dietary lapses.
How similar studies have performed: Other studies have shown promise in using real-time assessments and wearable technology to improve dietary adherence, suggesting that this approach may be effective.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Ages 18-70 * Body mass index (BMI) between 25 and 50 kg/m-squared Exclusion Criteria: * Has health problems for which weight loss or physical activity is contraindicated * Currently pregnant or breastfeeding * Currently or recently (\< 6 months) enrolled in a commercial weight loss program * Weight loss of ≥ 5% of initial body weight in the last 6 months * Currently taking weight loss medication, * Has history of surgical procedure for weight loss, * Has history of a clinically diagnosed eating disorder excluding Binge Eating Disorder
Where this trial is running
Providence, Rhode Island
- Weight Control and Diabetes Research Center — Providence, Rhode Island, United States (Recruiting)
Study contacts
- Study coordinator: Krystal Harvey, MS
- Email: kdefaria@lifespan.org
- Phone: 401-793-8991
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.