This study is a cooperative investigation funded by the NIH. The project is a collaboration among three major NIH Clinical Translational Science Awardees: 1) UCI (lead site with its affiliate CHOC), 2) Northwestern University (with its affiliate Lurie Children's Hospital), and 3) USC (with its affiliate Children's Hospital of Los Angeles). There is an increasing number of children who, through medical advances, now survive diseases and conditions that were once fatal, but which remain chronic and debilitating. A major challenge to improve both the immediate and long term care and health of such children has been the gap in our understanding of how to assess the biological effects of exercise. Like otherwise healthy children, children with chronic diseases and disabilities want to be physically active. The challenge is to determine what constitutes safe and beneficial level of physical activity when the underlying disease or condition \[e.g., cystic fibrosis (CF) or sickle cell disease (SCD)\] imposes physiological constraints on exercise that are not present in otherwise healthy children. Current exercise testing protocols were based on studies of athletes and high performing healthy individuals and were designed to test limits of performance at very high-intensity, unphysiological, maximal effort. These approaches are not optimal for children and adolescents with disease and disability. This project (REACH-Revamping Exercise Assessment in Child Health) is designed to address this gap. Cohorts of children will be identified with two major genetic diseases (CF and SCD) and measure exercise responses annually as they progress from early puberty to mid or late puberty over a 3-4year period. In addition, in the light of the pandemic, a group of children will be added who were affected by SARS-CoV-2 and investigate their responses to exercise. SARS-CoV-2 has similar long-term symptoms than CF and SCD have. Novel approaches to assessing physiological responses to exercise using advanced data analytics will be examined in relation to metrics of habitual physical activity, circulating biomarkers of inflammation and growth, leukocyte gene expression, and the impact of the underlying CF, SCD or SARS-CoV-2 condition. The data from this study will help to develop a toolkit of innovative metrics for exercise testing that will be made available to the research and clinical community.
New, generalizable approaches are needed for measuring physical fitness and activity across a spectrum of pediatric health and disease. Exercise in children and adolescents is not merely play but is an essential component of growth and development. Children are among the most spontaneously physically active human beings. It is not surprising that participation in PA (Physical Activity) is a major determinant of health across the lifespan and health-related quality of life in both healthy children and in children with chronic diseases. Despite this essential biologic role for PA, children have not been spared the relentless reduction in levels of PA that is creating a crisis in health care in our nation and throughout the world. Recognition of the enormous morbidity and cost of physical inactivity-related diseases, such as atherosclerosis, type 2 diabetes, and osteoporosis, has spurred new policy initiatives targeting preventive medicine early in life. The concept of pediatric origins of adult health and disease is gaining scientific merit, highlighting the need to transform existing notions of how to evaluate health in a growing child. A physically inactive (even normal weight) child may have no symptoms of disease, but evidence of deterioration in vascular health may already be present. As era of population health management and precision medicine are approaching, the notion of what it means to be a healthy child must change and include robust metrics of physical fitness. Equally worrisome is that the deleterious health effects of physical inactivity and poor fitness are exacerbated in children with chronic disease and/or disabilities or with environmental-lifestyle conditions like obesity. Children with diseases or conditions previously associated with mortality during the first two decades of life (e.g., SCD, CF) are living longer due to remarkable advances in research and care, but are often unable to achieve levels of PA and fitness associated with health benefits in otherwise healthy children. Not surprisingly, the healthspan \[the period of life free from serious chronic diseases and disability of children with chronic diseases is threatened not only by the underlying disease, but by the compounding effects of insufficient PA and sedentary behavior. Increasing PA and fitness is feasible, but has proven quite challenging to implement in a systematic manner. Once a pattern of physical inactivity and a sedentary lifestyle is established, a vicious cycle ensues, in which constraints on PA harm immediate health and contribute to lifelong health impairment ranging from cardiovascular and metabolic disease to osteoporosis. Exactly what constitutes ideal physical fitness in a child with a chronic condition remains unknown. Finding beneficial levels of PA in children with chronic disease or disability is challenging because the optimal range of exercise is much narrower than in a healthy child. Finally, as a result of the COVID-19 pandemic a sizable number of children are experiencing long-term effects such as fatigue, and will be included in our study. Similar to children with CF and SCD, studies of exercise and physical activity will provide insight into disease mechanisms and possible therapies.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
NONE
Enrollment
240
Cardiopulmonary Exercise Testing (CPET) will be used with Multiple Brief Exercise Bouts (MBEB) in order to obtain the necessary data to yield information on the study outcome variables
University of California, Irvine
Irvine, California, United States
RECRUITINGGas Exchange Variables
oxygen uptake
Time frame: 8 Months
Whole Body Lean Mass
Measured by Dual X-Ray Densitometry
Time frame: 8 Months
Physical Activity
Measured by Actigraphy
Time frame: 8 Months
Biomarkers
IGF-1
Time frame: 8 Months
Gene Expression
Circulating leukocyte gene expression associated with exercise
Time frame: 8 Months
Gas Exchange Variables
V̇O2
Time frame: 8 Months
Gas Exchange Variables
Carbon dioxide output
Time frame: 8 Months
Gas Exchange Variables
V̇CO2
Time frame: 8 Months
Gas Exchange Variables
ventilation
Time frame: 8 Months
Gas Exchange Variables
V̇E
Time frame: 8 Months
Gas Exchange Variables
heart rate (HR)
Time frame: 8 Months
Fat Mass
Measured by Dual Energy X-Ray Absorptiometry
Time frame: 8 Months
% Body Fat
Measured by Dual X-Ray Densitometry
Time frame: 8 Months
Whole Body Bone Mineral Content
Measured by Dual X-Ray Densitometry
Time frame: 8 Months
Whole Body Bone Mineral Density
Measured by Dual X-Ray Densitometry
Time frame: 8 Months
Biomarkers
IL6
Time frame: 8 Months
Biomarkers
C-Reactive Protein
Time frame: 8 Months
Biomarkers
Glucose
Time frame: 8 Months
Biomarkers
insulin
Time frame: 8 Months
Biomarkers
lipid screen
Time frame: 8 Months
Biomarkers
lactate
Time frame: 8 Months
Biomarkers
CBC
Time frame: 8 Months
Gene Expression
Circulating Leukocyte Gene Expression Associated with Sickle Cell Anemia
Time frame: 8 Months
Gene Expression
Circulating Leukocyte Gene Expression Associated with Cystic Fibrosis
Time frame: 8 Months
Behavioral responses to exercise
PROMIS Parent Fatigue Questionnaire
Time frame: 8 Months
Standardized assessments
TANNER Staging Questionnaire
Time frame: 8 Months
Behavioral responses to exercise
PROMIS Pediatric Fatigue Questionnaire
Time frame: 8 Months
Behavioral responses to exercise
Project REACH NHANES PAQ Adapted Questionnaire
Time frame: 8 Months
Behavioral responses to exercise
PEDSQL Fatigue Questionnaire
Time frame: 8 Months
Behavioral responses to exercise
Appendices Questionnaire
Time frame: 8 Months
Standardized assessments
Block Standardized FFQ
Time frame: 8 Months
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