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SubsTRate OxidatioN in Girls (STRONG)

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Pennington Biomedical Research Center

Status

Completed

Conditions

Overweight Adolescents

Treatments

Other: Acute exercise

Study type

Interventional

Funder types

Other

Identifiers

NCT04483921
PBRC 2020-003

Details and patient eligibility

About

This study will examine race differences in total energy expenditure and respiratory quotient (RQ) during and after exercise, compared to a sedentary control condition, in adolescent girls who are classified as overweight. In addition, subjective appetite and objective energy intake will be measured throughout the assessment periods.

Full description

Aim 1: Measure 24-hour energy expenditure and its components (resting, activity, and sleep energy expenditure) and compare differences between African-American and White girls.

Hypothesis: Total, resting, and sleep energy expenditure will be lower in African-American relative to White girls. Activity energy expenditure will be equivalent per the study design.

Aim 2: Measure and compare substrate oxidation and associations with appetite (i.e., hunger, desire to eat) and energy intake between African-American and White girls.

Hypothesis: African-American girls will have a higher RQ at rest, during exercise, and following exercise, and RQ will be positively associated with subjective appetite ratings and energy intake.

Enrollment

14 patients

Sex

Female

Ages

13 to 17 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Female
  • Age 13-17 years, inclusive
  • Achieved menarche based on parent- and/or self-report
  • Overweight based on BMI percentile for age and sex (≥ 85th and < 95th)
  • Self-identification as non-Hispanic White or African-American
  • Willing to maintain current physical activity, sleep schedule, and dietary habits during the study
  • Willing to comply with study procedures

Exclusion criteria

  • Contraindications to exercise testing as defined by the American College of Sports Medicine (i.e., medical history of cardiovascular, pulmonary, or physical conditions that affect the ability to exercise)
  • Food allergies
  • Dietary restrictions
  • Unwilling to consume study foods
  • History of polycystic ovary syndrome (PCOS)
  • Current amenorrhea or other menstrual cycle irregularities
  • Pregnant or currently breastfeeding
  • Current anemia
  • Use of medications affecting metabolism or sleep
  • Inability to properly or safely complete the study procedures per the investigators' discretion

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

None (Open label)

14 participants in 2 patient groups

Exercise
Experimental group
Description:
Participants will complete a prescribed exercise bout.
Treatment:
Other: Acute exercise
Sedentary
No Intervention group
Description:
Participants will rest quietly in a seated position for the equivalent amount of time prescribed for the exercise condition.

Trial contacts and locations

1

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Central trial contact

Nicole Fearnbach, PhD; Eric Ravussin, PhD

Data sourced from clinicaltrials.gov

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