- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07474818
Loaded and Task Specific Training in Spastic Diaplegic CP to Improve Gait and Functional Mobility. (ELTTS-GFM-SDCP)
Effects of Loaded Treadmill and Task Specific Training on Gait and Functional Mobility in Children With Spastic Diplegic Cerebral Palsy
Cerebral Palsy is a non-progressive condition caused by early brain injury that affects movement, posture, and muscle tone. Spastic diplegia mainly involves the lower limbs, leading to stiffness, weakness, and abnormal gait patterns.
These impairments reduce functional independence and increase caregiver burden. Loaded Treadmill Training and Task Specific Training are two rehabilitation approaches used to improve strength and Gait function.
This study compares their effectiveness in improving gait and functional mobility in children with spastic diplegic CP.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Misha Zahid Zahid, Doctor of Physicall Therapy
- Phone Number: 03277866777
- Email: misha.zahid@ubas.edu.pk
Study Locations
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Punjab Province
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Lahore, Punjab Province, Pakistan
- Lahore University of Biological Applied Health Sciences
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Confirmed diagnosis of Spastic Diplegic Cerebral Palsy
- 6 to 12 years
- Gross Motor Function Classification System Level I to III
- Stand independently or with support
Exclusion Criteria:
- Diagnosed with any type other then Spastic Diplegic
- Presence of Comorbidities
- Severe Cognitive and Communicative impairments
- Classified as Gross Motor Function Classification System Level IV and V
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Loaded Treadmil Training + Conventional Therapy
Participants in the intervention will receive Loaded Treadmill Training for 40 minutes, 3 times per week, for 6 weeks.
The session consists of three bouts of treadmill training with two 5-minute breaks.
The treadmill's walking speed will be increased gradually.
Additionally, conventional therapy will be given for 40 minutes 3 times per week, for 6 weeks
|
loaded treadmill training is a gait rehabilitation approach in which children walk on a treadmill while external loads (such as ankle weights) are applied to the lower limbs.
The load is gradually increased to enhance muscle strength, motor learning, and walking performance.
This intervention helps improve stride length, cadence, gait velocity, and overall functional mobility in children with spastic diplegic cerebral palsy.
|
|
Active Comparator: Task-Specific Training + Conventional Therapy
Participants in this arm will receive Task-Specific Training (TST) for 40 minutes per session, 3 times per week, for 6 weeks. The sessions will include a 5-minute warm-up, 30 minutes of functional activities (progressing in difficulty every two weeks), and a 5-minute cool-down. Additionally, participants will receive 40 minutes of Conventional Physical Therapy per session, 3 times per week for 6 weeks. |
Task-specific training is a rehabilitation approach based on repetitive practice of functional activities.
Children perform tasks such as standing, walking, stepping, and balance activities in a structured therapy program.
This approach aims to enhance coordination, strength, motor control, and functional mobility in children with spastic diplegic cerebral palsy.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Change in Gait Parameter: Cadence
Time Frame: Baseline and after 6 weeks
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Cadence, defined as the step rate or rhythm of the walk, will be measured in steps per minute.
This data will be collected and analyzed using the Jakcs Observational Gait Analysis, a 66-item clinical evaluation checklist designed to systematically observe, identify, and document abnormalities or deviations in patient walking patterns.
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Baseline and after 6 weeks
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Change in Gait Parameter: Velocity
Time Frame: Baseline and 6 weeks
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Walking velocity (speed) will be measured in meters per minute.
This parameter will be assessed and documented using the abbreviated 66-item Jakcs Observational Gait Analysis checklist.
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Baseline and 6 weeks
|
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Change in Gait Parameter: Stride Length
Time Frame: Baseline and after 6 weeks
|
Stride length, which is the measurement of the forward distance covered during two successive points of contact made by the same foot, will be measured in meters.
This will be recorded using the Jakcs Observational Gait Analysis tool.
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Baseline and after 6 weeks
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Change in Functional Mobility
Time Frame: Baseline and after 6 weeks
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Functional mobility will be assessed using Dimension E (Walking, Running & Jumping) of the Gross Motor Function Measure-88 (GMFM-88).
The GMFM-88 is a standardized observational instrument designed to assess functional mobility in children with cerebral palsy.
It has five dimensions.
The items in Dimension E are scored, and the total is calculated by averaging these percentages, where a higher percentage indicates better functional mobility and independence.
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Baseline and after 6 weeks
|
Collaborators and Investigators
Investigators
- Principal Investigator: Najam Zia Zia ul Haq, Doctor of Physical therapy, Lahore College of Physical therapy
- Principal Investigator: Laiba Nadeem Nadeem, Doctor of Physical Therapy, Lahore College of Physical therapy
- Principal Investigator: Ayesha Fatima, Doctor of Physical Therapy, Lahore College of Physical therapy
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- DPT/ERB/34
- U1111-1335-7052 (Registry Identifier: Laiba Nadeem)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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