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CompletedNCT03369691Updated Mar 13, 2026

Ethnic Influences on Stress, Energy Balance and Obesity in Adolescents

An observational study in Obesity, Adolescent, Stress and Physical Activity, sponsored by University of California, Irvine. Completed at 1 site in United States. Open to female participants aged 13 Years to 17 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-03-13.

Sponsored by University of California, Irvine · Observational

Study type
Observational
Model
Cohort
Time perspective
Cross-sectional
Enrollment
258
Ages
13 Years to 17 Years
Sex
Female
01

Study summary

The study will examine the mechanisms linking race, stress and biobehavioral factors to energy balance and obesity in both natural and controlled environments in African-American and Caucasian adolescent females. A Hispanic/Latina cohort has recently been added with permission for the sponsor.

Read the detailed description

Obesity is one of the most serious public health problems in the US; its prevalence has tripled in the last three decades and is associated with a range of short- and long-term medical and psychosocial problems. Adolescence is a critical period for the development and persistence of obesity, and is associated with changes in diet, physical activity and fitness, fat distribution and insulin sensitivity. There are racial and sex-specific disparities in the prevalence and burden of obesity. African-American (AA) females have the highest rates of obesity, and the clustered risk factors for coronary heart disease and metabolic syndrome are twice that of AA males. The reasons for racial and sex-specific disparities in the prevalence and burden of obesity are not well understood. AA experience higher stress levels than Non-Hispanic Whites (NHW) due to economic and social inequalities, and the effect of stress on energy-dense diet and adiposity is more prominent in females. A better understanding of the mechanisms that link stress to obesity, particularly during adolescence when high rates of obesity, increased stressful experiences and stronger behavioral and physiological responses to stress emerge, will contribute to new clinical guidelines for reducing obesity and associated medical conditions in AA females.

The Physiological stress system affects obesity and mediates its adaptive functions via hypothalamic-pituitary-adrenal (HPA) axis. Prolonged stress-induced glucocorticoid secretion promotes the consumption of energy-dense diet (EI) and abdominal fat deposition both directly and indirectly through its effects on metabolic hormones. Stress also reduces physical activity and alters energy balance. The proposed study will examine the effects of stress and HPA axis on EI and physical activity-related energy expenditure in 100 AA and 100 NHW adolescent females. The effects on EI will be assessed in two contexts, the natural environment and under controlled conditions incorporating a standardized psychosocial stressor. Stress will be assessed in the natural environment as multiple domains (i.e., individual, family and social), and several indices of the HPA axis will be obtained to represent diurnal variation, its status over 12-15 weeks and reactivity to stress. Obesity-related parameters will be measured through anthropometry, fat distribution and cardio-metabolic biomarkers.

Associations among stress, HPA activity/function, energy balance and obesity-related parameters will be compared between and within AA and NHW samples. In combination they will improve our understanding of the social factors and biobehavioral mechanisms of both racial and individual differences in obesity and facilitate the development of effective treatments within and across racial groups according to the principles of individualized medicine. To our knowledge, racial differences in objectively-measured diet intake and energy expenditure in response to stress, or their underlying physiological mechanisms, have not been assessed in adolescents or adults. This is an important knowledge gap in our efforts to develop better evidence-based translational obesity prevention and weight-control interventions as the traditional interventions are not effective with minority youth.

02

Conditions studied

  • Obesity, Adolescent
  • Stress
  • Physical Activity
03

Who can participate

Ages eligible
13 Years to 17 Years
Sexes eligible
Female
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Community sample

Inclusion criteria

  • African-American, Hispanic, Non-Hispanic White females from 13-17 years old and Tanner Stage ≥III.
  • BMI values will be balanced (1/3rd normal, 1/3rd overweight and 1/3rd obese range percentile BMI values) using Center for Disease Control criteria

Exclusion criteria

Exclusion Criteria:

  • Participants with a BMI below the normal range, trying to lose weight, on medications that affect appetite or hypothalamic-pituitary-adrenal axis, or with a history of bariatric surgery, will be excluded.
  • Restrained or binge eaters, individuals who score below 50 on a 100 mm Visual Analog Scale for foods provided in the study, or those allergic to these foods will be excluded.
  • Participants with major psychiatric disorders (e.g., anxiety, eating, mood, substance use disorders) or medical problems (e.g., endocrine disorders or unstable cardiac, pulmonary or renal conditions) will be excluded.
  • Pregnant females, or those suspected of being pregnant, will be excluded.
04

Study design

Observational model
Cohort
Time perspective
Cross-sectional
Enrollment
258 participants (actual)
Patient registry
No
Biospecimen retention
Samples without dna
05

What researchers measure

Primary outcomes

  1. Comparison of food intake from buffet lunch after the control and stress sessions

    Randomize lab session to assign each participant to a non-stress or stress condition, and reversed in the next session. Ad-libitum food intake (amount of added sugar and solid fat) during both sessions will be measured and compared.

    Time frame: 7 days between the two sessions

Secondary outcomes

  1. Body mass index (BMI)

    Weight (kg) and height (inches) will be used to determine BMI in kg/cm\^2

    Time frame: 1 hour

  2. Physical activity energy expenditure

    Average moderate and vigorous activity (minutes) will be recorded through the Actigraph device

    Time frame: 7 days

  3. Visceral fat percent

    Amount of visceral fat (percent of total fat) will be determined by dual-energy x-ray scan

    Time frame: 1 hour

06

Study locations

1 site
  • Universty of California, Irvine
    Irvine, California 92617, United States
07

References and documents

Study documents

  • Informed consent form · Dec 19, 2024

Documents are hosted by the registry — open the source record to download them.

Individual participant data

Plan to share: No

08

Registry details

Key details

Study ID
NCT03369691
Lead sponsor
University of California, Irvine
Responsible party
Uma Rao (Professor, University of California, Irvine) — Principal investigator
First posted
Dec 12, 2017
Start date
Dec 16, 2017
Primary completion
Feb 7, 2026
Completion
Feb 7, 2026
Last update
Mar 13, 2026

Study contacts

Uma Rao, MD
principal investigator · University of California, Irvine

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Mar 2026. You cannot join it, but the record below documents what was studied.

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