Childhood Obesity Clinical Trial
Official title:
The Effect of Exercise With AR Glasses on Metabolic Parameters and Anthropometric Measurements in Obese Adolescents
This study was planned as a randomized controlled experimental study to determine the effect of exercise with Augmented Reality Goggles (AR) on metabolic parameters and anthropometric measurement values in obese children aged 10-19 years. The study will be conducted with children diagnosed with obesity between the ages of 10-19 years who are followed up in the Pediatric Endocrinology Outpatient Clinic of Erciyes University Health Application and Research Center Fevzi Mercan-Mustafa Eraslan Children's Hospital. According to the sample calculation, a total of 20 obese children aged 10-19 years (AR exercise group=10 and control group=10) will be included in the sample of the study. The data of the study will be collected using the Descriptive Characteristics Form for Obese Children and Their Families, Serum and Urine Biochemistry Values Form, Anthropometric Measurement Values Form, Augmented Reality Goggles, Body Composition Analyzer, Caliper, Tape Measure and Digital Height and Weight Measurement Device. Ethics committee permission was obtained from "Erciyes University Clinical Research Ethics Committee" and institutional permission was obtained from ERU Health Practice and Research Center Mustafa Eraslan Fevzi Mercan Children's Hospital. Hypothesis tests, correlation and regression analyzes will be applied according to the suitability of the data for normal distribution. As a result of the study, it is expected that exercise application with AR glasses will improve metabolic parameters and anthropometric measurement values in obese children.
Status | Recruiting |
Enrollment | 20 |
Est. completion date | March 1, 2024 |
Est. primary completion date | January 1, 2024 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 10 Years to 19 Years |
Eligibility | Inclusion Criteria: - Those between the ages of 10-19, - Having been diagnosed with childhood obesity at least six months ago, - Do not have any other chronic disease, - No psychiatric diagnosis, - No orthopedic problems, - Able to read and write - Can speak Turkish, - No mental, physical or neurological disability, - Residing in the province where the research will be conducted, - Children and children with parental consent to participate in the study will be included in the study. Exclusion Criteria: - |
Country | Name | City | State |
---|---|---|---|
Turkey | Erciyes University | Kayseri |
Lead Sponsor | Collaborator |
---|---|
TC Erciyes University |
Turkey,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in serum leptin levels | Serum leptin of children with type 1 diabetes before, during, after exercise and during the control session. | Change in average serum leptin over 12-week sessions | |
Primary | Change in serum irisin levels | Serum irisin of children with type 1 diabetes before, during, after exercise and during the control session. | Change in average serum irisin over 12-week sessions | |
Primary | Change in body mass index | Average body mass index values of children with obesity before, during, after exercise and during the control session. | Change in average body mass index over 12-week sessions |
Status | Clinical Trial | Phase | |
---|---|---|---|
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