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Clinic, Family & Community Intervention for Children With Overweight and Obesity (Stanford GOALS)

Clinic, Family & Community Collaboration to Treat Overweight and Obese Children

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01642836
Enrollment
241
Registered
2012-07-17
Start date
2012-07-13
Completion date
2016-12-19
Last updated
2021-05-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Obesity

Brief summary

Stanford GOALS is a large-scale, community-based randomized controlled trial of an innovative, interdisciplinary, multi-component, multi-level, multi-setting (MMM) approach to treating overweight and obese children. Primary Research Question: Will a 3-year, innovative, interdisciplinary, multi-component, multi-level, multi-setting (MMM) community-based intervention to treat overweight and obese children significantly reduce BMI compared to an enhanced standard care/health and nutrition education active comparison intervention?

Detailed description

Single-blind study with all outcomes assessors (data collectors) and Investigators masked (blinded) to intervention assignment. Intention-to-treat analysis.

Interventions

BEHAVIORALMMM

1. a theory-based community team sports program designed specifically for overweight and obese children, 2. a home-based family intervention to reduce screen time, alter the home food/eating environment, and promote self-regulatory skills for eating and activity behavior change, and 3. a primary care provider behavioral counseling intervention linked to the community and home interventions.

BEHAVIORALHealth and Nutrition Education

Enhanced standard care/health and nutrition education intervention: 1. notification of primary care providers about metabolic measures and blood pressure 2. state-of-the-art information-based health and nutrition education, including semi-annual home counseling visits, monthly health education newsletters for children and for parents/guardians, and a series of quarterly, community-based evening health lectures and Family Fun Nights

Sponsors

National Heart, Lung, and Blood Institute (NHLBI)
CollaboratorNIH
Stanford University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
7 Years to 11 Years
Healthy volunteers
Yes

Inclusion criteria

* 7-11 years of age * BMI greater than or equal to the 85th percentile for age and sex on the 2000 U.S. Centers for Disease Control and Prevention (CDC) BMI reference

Exclusion criteria

* Have been diagnosed with a medical condition affecting growth (a genetic or metabolic disease/syndrome associated with obesity, Type 1 diabetes, Type 2 diabetes taking medication, chronic gastrointestinal diseases, Chronic renal diseases, uncorrected structural heart disease, heart failure, heart transplant, anorexia nervosa or bulimia nervosa or binge eating disorder (present or past), AIDS or HIV infection, pregnancy); * Take medications affecting growth (systemic corticosteroids more than 2 weeks in the past year, insulin, oral hypoglycemics, thyroid hormone, growth hormone); * Have a condition limiting their participation in the interventions (e.g., unable to participate in routine physical education classes at school, requiring oxygen supplementation for exertion, developmental or physical disability preventing participation in interventions, children or parents/guardians who cannot medically participate in mild dietary restrictions and/or increased physical activity for any reason); * Have a condition limiting participation in the assessments (child or primary caregiver not able to read surveys in English or Spanish, child two or more grade levels delayed in school for reading and writing in her native language); * Are unable to read, understand or complete informed consent in English or Spanish; * Plan to move from the San Francisco Bay Area within the next 36 months. * Are deemed to have another characteristic that makes them unsuitable for participation in the study in the judgment of the Principal Investigator.

Design outcomes

Primary

MeasureTime frameDescription
body mass index trajectory (change)baseline, 1, 2 and 3 yearsslope of measured weight in kilograms divided by the square of height in meters

Secondary

MeasureTime frameDescription
triceps skinfold thicknessbaseline, 1, 2 and 3 yearstriceps skinfold thickness in mm
Percent median BMI for age and sex (calculated from BMI)baseline, 1, 2, and 3 yearsage- and sex-adjusted BMI
Waist-to-Height Ratiobaseline, 1, 2 and 3 yearscalculated from waist and height measures
Percent body fat (estimated)baseline, 1, 2, and 3 yearsEstimated from regression equation
fasting Total Cholesterol, LDL-Cholesterol, HDL-Cholesterol, Triglycerides, Insulin, glucose, hemoglobin A1c, high sensitivity C-Reactive Protein, Alanine Aminotransferase (ALT)baseline, 1, 2 and 3 yearslab assays of fasting samples
resting blood pressurebaseline, 1, 2 and 3 yearsautomated resting blood pressure
resting heart ratebaseline, 1, 2 and 3 yearsautomated pulse
physical activity measured by accelerometrybaseline, 1, 2 and 3 yearsActigraph model GT3X+ total and after school physical activity and sedentary behavior
screen time and other sedentary behaviorsbaseline, 1, 2 and 3 yearsself-reported weekday, saturday and sunday, television, movies, video games, computer, portable media devices, mobile phones
Typical household Television (TV) usebaseline, 1, 2, and 3 yearsConstant TV household measure
Average total daily energy intakebaseline, 1, 2 and 3 yearsfrom 24 hour diet recalls
Percent of energy intake from fatbaseline, 1, 2, and 3 yearsfrom 24 hour diet recalls
waist circumferencebaseline, 1, 2 and 3 yearswaist circumference in centimeters
Eating with screensbaseline, 1, 2, and 3 yearsbreakfast, dinner and energy (from 24-hour diet recalls)
Depressive symptomsbaseline, 1, 2 and 3 yearsChildren's Depression Index short form
Weight Concernsbaseline, 1, 2 and 3 yearsOverconcern with weight and shape scale
School performancebaseline, 1, 2 and 3 yearsparent/guardian reported grades
Children's sleep habitsbaseline, 1, 2 and 3 yearsparent/guardian reported
Implicit theoriesbaseline, 1, 2, and 3 yearsfixed versus growth mindset
Parent/guardian weightbaseline, 1, 2, and 3 yearsmeasured weight
Parent/guardian body mass indexbaseline, 1, 2, and 3 yearscalculated from measures of height and weight
Parent/guardian waist circumferencebaseline, 1, 2, and 3 yearswaist circumference measured in cm
Parent/guardian reported physical activitybaseline, 1, 2, and 3 yearssurvey
Parent/guardian health literacybaseline, 1 and 2 yearsNew Vital Sign (NVS) measure
Added sugarbaseline, 1, 2, and 3 yearsfrom 24 hour diet recalls

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 2, 2026