Assessing the Impact of Task-Oriented Training Rooted in Neurodevelopmental Therapy Principles on Gait and Daily Functional Activities in Cerebral Palsy
- Conditions
- Health Condition 1: F01-F99- Mental, Behavioral and Neurodevelopmental disorders
- Registration Number
- CTRI/2024/05/066622
- Lead Sponsor
- Galgotias University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Age Range: Children and adolescents aged between 5 and 12 years.
Diagnosis: Participants must have a confirmed diagnosis of cerebral palsy by a qualified medical professional.
Type of Cerebral Palsy: Children and adolescents with any type of cerebral palsy (spastic, dyskinetic, ataxic, or mixed) are eligible for inclusion.
Gait Impairment: Individuals should exhibit gait abnormalities, such as altered stride length, step width, or gait velocity, that affect their functional mobility.
Ability to Walk: Participants must be capable of walking independently or with the use of assistive devices, such as walkers or crutches.Medical Stability: Individuals should be medically stable and free from any acute medical conditions that could interfere with participation in the training program.
Ability to Follow Instructions: Participants should have the cognitive and communicative ability to understand and comply with the instructions during the training sessions.
Severe Cognitive Impairment: Participants with severe cognitive impairments or intellectual disabilities that would hinder their ability to actively participate in the task-oriented training program will be excluded.
Severe Communication Difficulties: Individuals with significant communication difficulties, making it challenging to understand or follow instructions during the training sessions, will be excluded.
Uncontrolled Medical Conditions: Participants with uncontrolled medical conditions, such as uncontrolled seizures or active infections, that could compromise their safety or interfere with the study outcomes will be excluded.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Motion analysis tool (Gaiton)Timepoint: 8 week
- Secondary Outcome Measures
Name Time Method The Functional Mobility Scale (FMS)Timepoint: 8 week