Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
14 participants
INTERVENTIONAL
2020-07-15
2023-10-20
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
The Effect of Exercise and/or Diet on Health Related Parameters
NCT04100356
Time-restricted Eating and High Intensity Interval Training Among Women
NCT04019860
The Effects of a Combined Exercise Training Program on Vascular Health and Metabolic Profile in Obese Adolescent Girls.
NCT03146026
Effects of Fasted- Versus Fed-exercise on Metabolic Health in Physically Active Adults
NCT06949709
Effects of Resistance Training on Substrate Metabolism During the Menstrual Cycle
NCT04024826
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
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.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
CROSSOVER
BASIC_SCIENCE
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Exercise
Participants will complete a prescribed exercise bout.
Acute exercise
Participants will complete a morning exercise bout at 70% of their individual maximal aerobic capacity to burn 200 kilocalories above their basal metabolic rate.
Sedentary
Participants will rest quietly in a seated position for the equivalent amount of time prescribed for the exercise condition.
No interventions assigned to this group
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Acute exercise
Participants will complete a morning exercise bout at 70% of their individual maximal aerobic capacity to burn 200 kilocalories above their basal metabolic rate.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* 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
* 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
13 Years
17 Years
FEMALE
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Nutrition Obesity Research Center
OTHER
Pennington Biomedical Research Center
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Eric Ravussin
Professor
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Eric Ravussin, PhD
Role: PRINCIPAL_INVESTIGATOR
Professor
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Pennington Biomedical Research Center
Baton Rouge, Louisiana, United States
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
PBRC 2020-003
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.