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NCT07839832Recruiting

Stanford Healthy Goals Study

Wise Social Psychological Interventions to Improve Outcomes of Behavioral Weight Control in Children With Obesity

Source: ClinicalTrials.gov · Last updated 28 Sept 2026

Brief summary (registry, in English)

Past modest, transient and highly variable outcomes from many behavioral treatments for pediatric obesity may be, in part, because of the psychological barriers children with obesity face when trying to control their weight. The goal of this randomized controlled trial is to test whether adding two innovative, brief, social psychological activities (termed "wise" interventions) to a high quality, family-based, group behavioral weight control program, will produce better outcomes among participating children with obesity. The primary hypothesis is that children who receive the family-based, group, behavioral weight control program plus the wise social psychological interventions will have significantly less body mass index growth over 12 months than children who receive the family-based, group, behavioral weight control program plus additional educational content. Participants will be asked to do participate in the six month treatment program and complete measurements at the beginning of the study, after 3 months, after 6 months (the end of the behavioral treatment program), and after 12 months (6 months after completing the behavioral treatment program). This study has the potential to substantially improve the outcomes of pediatric weight control treatments and significantly reduce concurrent and future health, psychological and social harms from childhood obesity.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
200 (estimated)
First submitted
18 Sept 2026
Start date
Jan 2027
Primary completion date
Feb 2030
Lead sponsor
Stanford University
Diseases
Obesity
NCT number
NCT07839832

What you commit to

  • Study type: Interventional
  • Planned participants: 200
  • From Jan 2027 to the primary completion date, Feb 2030
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Medications affecting growth

Other illness

  • Medical conditions affecting growth
  • Conditions limiting participation in the interventions
  • Conditions limiting participation in the assessments

Other

  • Unable to read, understand or complete informed consent in English or Spanish
  • Other exclusion as deemed by the investigators

Who the study is looking for

  • 10-15 year old children
  • Obesity (BMI ≥ 95th percentile on the 2000 Centers for Disease Control and Prevention BMI reference) on the date of randomization.
  • Child and at least one parent/guardian must agree to participate

Age in the registry: 10 years to 15 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Stanford University
Coordinator of this site? Confirm its status
StanfordUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.