Dry Needling for Spasticity in Children with Cerebral Palsy
Traditional Physical Therapy
+ Dry Needling
Brain Damage, Chronic+10
+ Brain Diseases
+ Central Nervous System Diseases
Treatment Study
Summary
Study start date: February 20, 2025
Actual date on which the first participant was enrolled.This study is focused on exploring how dry needling, a technique used to relax tight muscles, can help children with cerebral palsy who experience spasticity. Spasticity in this context refers to the stiffness and involuntary muscle contractions that can limit movement and balance. By targeting the overactive muscle fibers, dry needling might reduce muscle tightness and improve the ability to move and perform daily activities. This research is important because it could offer a new way to help children with cerebral palsy improve their muscle function and overall quality of life. Participants in the study will receive dry needling treatment aimed at specific muscle groups that are affected by spasticity. The effectiveness of this intervention will be measured using several tests. The Modified Ashworth Scale (MAS) will be used to check changes in muscle tone, the Timed Up and Go (TUG) test will evaluate mobility and balance, and the Gross Motor Function Measure (GMFM) will assess overall movement skills. By comparing results before and after the treatment, the study aims to find out if dry needling can provide real benefits, potentially making it a useful addition to current rehabilitation strategies for children with neuromuscular disorders.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.48 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.Over 6 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