Virtual Reality vs. Video Assisted Exercises in Pediatric Chronic Kidney Disease
This study aims to compare the effectiveness of Virtual Reality exercises versus Video Assisted exercises in improving functional capacity and muscle strength in children with Chronic Kidney Disease.
study group
+ control group
Behavior
+ Motor Activity
Treatment Study
Summary
Study start date: July 30, 2018
Actual date on which the first participant was enrolled.This study focuses on comparing the effectiveness of two different exercise methods for children with chronic kidney disease. The goal is to improve their functional capacity, muscle strength, quality of life, and other health aspects. One group will use virtual reality technology, specifically Nintendo Wii Fit Plus, while the other group will do home-based video exercises. This research is important as it aims to find the best exercise approach to help children with this condition, potentially improving their overall health and well-being. The virtual reality group will participate in 12 sessions of 30-minute exercises, including strengthening exercises for the upper and lower body, aerobic exercises, and balance exercises. Each session will start with a 5-minute warm-up, end with a 5-minute cool-down and breathing exercises, making a total of 50 minutes. The home-based video exercise group will follow a similar exercise routine at home for 30 minutes, two days a week. Both groups will also track their daily physical activities like walking, cycling, or swimming. The study will measure the results by assessing functional capacity through a 6-minute walking test and muscle strength using a digital dynamometer at the beginning and after 6 weeks.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.16 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Treatment Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.From 6 to 18 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.2 intervention groups are designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalGroup II
Active ComparatorStudy Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
Istanbul University of Health Sciences Kanuni Sultan Süleyman Training and research Hospital
Istanbul, Turkey (Türkiye)Open Istanbul University of Health Sciences Kanuni Sultan Süleyman Training and research Hospital in Google Maps