Upper-extremity Plyometrics for Muscle Strength in Children With Hemiparetic Cerebral Palsy
Plyometric Exercise
+ Standard exercise program
Brain Damage, Chronic+2
+ Brain Diseases
+ Central Nervous System Diseases
Treatment Study
Summary
Study start date: February 12, 2023
Actual date on which the first participant was enrolled.This study focuses on improving muscle strength and movement abilities in children with hemiparetic cerebral palsy, a condition that affects movement on one side of the body. It involves children aged 10 to 15 years who have mild to moderate movement challenges and are receiving treatment at a university clinic and hospitals in Saudi Arabia. The aim is to determine if a specific exercise program, called Plyo-Ex, can enhance their strength and functionality better than the usual exercises they are given. This research is important because it could lead to more effective therapies that help children with this condition improve their physical abilities and overall quality of life. In this study, participants are divided into two groups. One group follows the Plyo-Ex training program, which includes exercises like push-ups and ball activities, twice a week for 12 weeks, with each session lasting 45 minutes. The other group follows a standard exercise routine. The effectiveness of these programs is evaluated by measuring muscle strength through specific devices and assessing hand function using recognized performance tests. By comparing the outcomes between the two groups, researchers aim to identify which program is more beneficial. The study ensures all activities are safe and adhere to established guidelines, minimizing any potential risks for the participants.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.58 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 10 to 15 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