Renal Insufficiency, Chronic
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Resident students at the Federal Institute of Rondônia, Ariquemes Campus; of either gender; regularly enrolled in the first year of integrated high school programs; under 18 years of age throughout the study period; submission of the Informed Consent Form signed by a legal guardian; submission of the Informed Assent Form signed by the participant
Exclusion criteria
Exclusion criteria: Psychological disorders preventing comprehension of research procedures; lower-limb amputation or disability; pregnancy; high cardiovascular risk; musculoskeletal complications contraindicating physical exercise; issues identified in the Physical Activity Readiness Questionnaire (PAR-Q) that contraindicate participation; or any clinical condition or other relevant factor identified by the researchers that could compromise participant safety or interfere with the implementation of the intervention and assessments
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Expected outcome 1: An increase in glomerular filtration rate is expected, estimated by measuring serum cystatin C concentration using the Pierce equation, assessed at the beginning of the first two months and at the end of the second two months after sixteen weeks of combined physical exercise intervention | — |
Secondary
| Measure | Time frame |
|---|---|
| Expected outcome 1: A reduction in glycated hemoglobin, assessed using an immunoturbidimetric method certified by the National Glycohemoglobin Standardization Program, is expected to be observed between the beginning of the first two-month period and the end of the second two-month period;Expected outcome 2: An increase in high-density lipoprotein concentration, determined by an automated enzymatic method, is expected at the beginning of the first two-month period and at the end of the second two-month period;Expected outcome 3: A reduction in low-density lipoprotein concentration, determined by an automated enzymatic method, is expected at the beginning of the first two-month period and at the end of the second two-month period;Expected outcome 4: A reduction in systolic blood pressure measured by sphygmomanometry is expected at the beginning of the first two months and at the end of the second two months;Expected outcome 5: A reduction in diastolic blood pressure measured by sphygmomanometry is expected at the beginning of the first two months and at the end of the second two months;Expected outcome 6: Increased muscle mass and reduced body fat percentage, as assessed by bioelectrical impedance analysis, are expected at the beginning of the first two months and at the end of the second two months;Expected outcome 7: It is expected that there will be a reduction in abdominal circumference and an improvement in the waist-to-height ratio and waist-to-hip ratio, as assessed by anthropometry, at the beginning of the first two months and at the end of the second two months;Expected outcome 8: It is expected that urine specific gravity will remain within normal values ??as assessed by refractometry at the beginning of the first two months and at the end of the second two months;Expected outcome 9: A reduction in anxiety symptoms, as assessed by the Depression, Anxiety, and Stress Scale for Adolescents, is expected at the beginning of the first term and at the end of the | — |
Countries
BR
Contacts
Instituto Federal de Educação, Ciência e Tecnologia de Rondônia (IFRO)