Pediatric Obesity Clinical Trial
Official title:
The Role of Exercise and/or Diet in Weight Loss, and Weight Maintenance in Obese Preadolescent Children
A 3-arms randomized prospective intervention study to determine the roles of exercise and/or
diet on weight loss and weight maintenance in obese preadolescent children 6-11 year-old
with BMI> 95th percentile for age and gender. Children were randomly allocated into three
groups. The first group underwent an exercise program, the second one underwent both an
exercise program and a diet program and the third underwent a diet program alone.
The total duration of the intervention is 12 weeks followed by a period of 9 months of
follow-up. The effects of the different intervention on weight loss and weight
maintenance,body composition, on hormonal components that regulate the caloric balance, on
metabolic profile and cardiovascular risk factors and on psychological parameters were also
determined.
A 3-arms randomized prospective intervention study including 161 patients in order to
determine the roles of exercise and/or diet on weight loss and weight maintenance in obese
preadolescent children 6-11 year-old with BMI> 95th percentile for age and gender. The study
recruited patients from 2 endocrine clinics.
Objectives:
1. The main aim was to determine the roles of exercise and/or diet on weight loss and
weight maintenance in obese children.
2. Secondary goals were:
1. To determine the effects of exercise and/or diet on body composition.
2. To determine the effects of exercise and/or diet on leptin and ghrelin that play a
role in the regulation of energy balance.
3. To determine the effects of exercise and/or diet on metabolic profile,
cardiovascular risk factors, and inflammatory markers as fasting glucose,insulin
and lipid profile,homocysteine ,adiponectin levels,CRP,and IL-6.
4. To determine the role of exercise and/or diet on psychological parameters of obese
children.
Study Population
Inclusion Criteria
1. Obese preadolescent children 6-11 year-old with BMI> 95th percentile for age and
gender.
2. A signed informed consent will be taken from patients and their parents.
3. Agreement to a follow-up of one year.
Exclusion Criteria
1. Cardiac problems (arrhythmia, Congestive heart disease)
2. Uncontrolled hypertension
3. Severe hepatic impairment (liver enzymes above 3 folds the upper normal values)
4. Renal failure
5. Genetic syndromes associated with obesity
6. Presence of untreated hypothyroidism
7. Participation in a clinical study during the last month methods Children fulfilling the
inclusion and exclusion criteria were randomly allocated into one of three groups.
The first group underwent an exercise program, the second one underwent both an exercise
program and a diet program and the third underwent a diet program alone.
On the first visit of the study, at the end of the intervention (12 weeks) and at the end of
the follow-up period (1 year) the following had been checked:
Weight, Height, Body impedance, Waist and hip circumferences, Skin-folds, Blood pressure,
Basal Metabolic Rate (evaluated by a metabolic monitor), and blood samples for: Blood count,
Liver function, Renal function, Fasting Lipid, glucose and insulin,CRP, IL-6, TSH, free T4,
Homocysteine, Adiponectin, Leptin and Ghrelin. Also at these point of time every patient
underwent a psychosocial evaluation with life style questioners.
Safety:There were no complications with these modes of treatment.
;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
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