An Online Intuitive Eating Program for Pregnant Women With Obesity
Official title: Feasibility and Preliminary Effects of an Online Intuitive Eating Intervention on Gestational Weight Gain and Well-Being in Pregnant Women
Run by San Diego State University · NCT07792837 · Data updated 2026-11-12
A 8-week online intuitive eating program is being tested to see if it helps pregnant women with obesity manage weight gain and improve well-being.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | Women only |
| Enrollment | 80 (estimated) |
| Sponsor | San Diego State University Academic / other |
| Locations | 2 sites (San Diego, California and 1 other locations) |
| Status | Recruiting |
| Started | November 2026 |
| Main results expected | August 2027 |
| Study ends | December 2027 |
| Registry record updated | November 6, 2026 |
| Trial ID | NCT07792837 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Pregnant adults aged 18 or older, 12 to 22 weeks gestation at enrollment, with pre-pregnancy BMI of 30.0 kg/m2 or higher, English literacy, and reliable internet access, receiving care at UCSDHealth or affiliated sites.
✕Probably not a fit
Individuals without access to a compatible device or who are in high-risk pregnancies or with certain medical/psychiatric exclusions may not experience benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This is a pilot feasibility study enrolling about 80 pregnant participants with a pre-pregnancy BMI of 30 or higher. Participants are randomized 1:1 to the intuitive eating intervention or a wait-list control, delivered asynchronously over 8 weeks. Feasibility will be measured by acceptability, demand, retention, and engagement, while preliminary effects will explore gestational weight gain, eating behaviors, dietary quality, body image, stress, and mental health. The intervention is adapted from the Tribole and Resch intuitive eating framework and is delivered through an online platform. Outcomes will inform whether a larger trial is warranted and how the program might be refined for pregnant individuals with obesity.
Why it matters
Potential benefit: If successful, the program could help pregnant individuals with obesity manage weight gain and improve mental well-being and dietary quality.
How similar studies have gone: There is emerging interest in applying intuitive eating during pregnancy, but this specific online PIE-I approach in obese pregnant people is among early feasibility investigations.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Age ≥18 years * Pregnant women between 12 weeks and \<22 weeks gestation * Pre-pregnancy BMI 30.0 kg/m² or greater * Able to read and understand English (for intervention materials and questionnaires) * Receiving prenatal care at UC San Diego Health (UCSD) * Reliable access to a device (e.g., smartphone, tablet, or computer) with internet connection Exclusion Criteria: * Current or past diagnosis of an eating disorder (e.g., anorexia nervosa, bulimia nervosa, binge eating disorder, ARFID) * High-risk pregnancy or medical complications that may significantly affect diet, physical activity, or weight gain (e.g., gestational diabetes requiring insulin, preeclampsia, hyperemesis gravidarum) * Multiple gestation pregnancy (e.g., twins or higher-order multiples) * Current participation in another nutrition, weight management, or behavioral intervention study * Severe psychiatric illness (e.g., schizophrenia, bipolar disorder) or current substance use disorder that would interfere with participation * Inability to provide informed consent or comply with study procedures
Where it's running
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San Diego State University
San Diego, California, United States Recruiting -
UC San Diego Health
San Diego, California, United States Recruiting
Study contacts
- Study coordinator: Jeni Green, PhD
- Email: jgreen5@sdsu.edu
- Phone: 619-594-6489
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.