Pediatric Obesity Clinical Trial
Official title:
Bone Health of Obese Adolescents During Weight Loss
The long-term goal of this proposal is to understand the impact of obesity and obesity
treatment on bone health during adolescence and how to preserve it. The recent pediatric
obesity epidemic raises important clinical and public health questions about the effects of
childhood-onset obesity and its treatment on bone health. Osteoporotic fractures are a major
cause of morbidity and mortality in the aged, and peak bone mass (PBM), achieved shortly
after puberty, is a key determinant of bone strength and lifetime fracture risk. Given the
current obesity epidemic, obesity treatment during adolescence will continue to be
necessary. The benefits of pediatric obesity treatment are unquestionable. However, the
potential detrimental effects of weight loss on bone density and dimensions are not known in
adolescents and are the focus of this proposal.
This study will focus on the impact of pediatric-onset obesity and its treatment on bone
health, using two approaches: comparing obese and non-obese adolescents and comparing obese
adolescents before and after weight loss. We hypothesize that (a) compared to non-obese
controls, obese adolescents have stronger bones, and that (b) bone strength of obese
adolescents decreases during weight loss compared to usual care, which would suggest a need
to promote bone health during successful weight loss in obese adolescents.
Context: The childhood obesity epidemic raises important clinical and public health questions about the effects of both obesity and obesity treatment on bone development. Osteoporotic fractures are a major cause of morbidity and mortality in the aged. However, peak bone mass, achieved shortly after puberty, is the key determinant of lifetime osteoporotic fracture risks. The size and direction of effects of obesity and weight loss on bone health in childhood are unclear, partly because of bone ascertainment issues. Obese children and adolescents may have elevated fracture risks, contrary to expectations based on adult data. Objectives: Primary aims of the proposed study are to: 1) characterize and compare bone health of obese and non-obese adolescents using the most accurate methods available, and 2) investigate the impact of comprehensive behavior weight control program on the bone health of obese adolescents. Study Design: Aim 1 will use a case-control design to compare bone status measures of 88 obese adolescents (ages 10 to 14 years), to be recruited for a randomized obesity treatment trial, with the same measurements of 51 contemporary non-obese control adolescents. For Aim 2, the 88 obese adolescents will be enrolled in a 12-month randomized trial, with 1:1 assignment, of a comprehensive behavioral weight control program vs. individualized nutrition education (usual care). This randomized trial is the object of this registration. Study Measures: For both aims the primary outcome will be bone strength, estimated by stress-strength index, and measured by peripheral quantitative computerized tomography (pQCT) at the tibia, a weight-bearing site. ;
Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
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