- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05068596
Effect of Loaded Functional Training on Hemiplegic Cerebral Palsy
April 6, 2022 updated by: hanaa mohsen, Badr University
Influence of Loaded Functional Strength Training From a Plantigrade Foot Position Using Shoe Holder on Hip and Knee Extensors Strength and Function Walking Capacity in Children With Spastic Hemiplegic Cerebral Palsy
weakness of lower limb is common in cp children
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
72
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Cairo, Egypt
- Hanaa Mohsen Abd-Elfattah
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
10 years to 12 years (Child)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- age 10-12
- level I,II according to GMFCM
- Able to follow and understand instructions
Exclusion Criteria:
- visual and respiratory disorder
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
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: study groip
received the designed physical therapy program as the control group.
In addition, they received progressive resistive functional strength training in the plantigrade foot position.
|
progressive resistive functional strength training in the plantigrade foot position plus designed physical therapy program
|
|
Other: control group
received a designed physical therapy program
|
Designed physical therapy program
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Muscle strength dynamometry
Time Frame: pre and post three month of intervention high score indicate improvement
|
The gold standard for evaluating isometric muscle strength is the portable dynamometer
|
pre and post three month of intervention high score indicate improvement
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Hanaa M Abd-Elfattah, ph.d, lecturer
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
September 30, 2021
Primary Completion (Actual)
December 31, 2021
Study Completion (Actual)
January 15, 2022
Study Registration Dates
First Submitted
September 12, 2021
First Submitted That Met QC Criteria
September 24, 2021
First Posted (Actual)
October 6, 2021
Study Record Updates
Last Update Posted (Actual)
April 13, 2022
Last Update Submitted That Met QC Criteria
April 6, 2022
Last Verified
February 1, 2022
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- hana 9
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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