Effect of Vibration on Shoulder Proximal Stability in Children With Cerebral Palsy
NCT ID: NCT07096089
Last Updated: 2025-07-31
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
50 participants
INTERVENTIONAL
2023-10-10
2024-04-10
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Methods: Fifty children with cerebral palsy from 4 to 9 years old participated in this study and were selected from the outpatient clinic of faculty of physical therapy. They were divided into two groups of equal sizes randomly. The control group received a conventional physical therapy program in addition to Sling exercise therapy, and the study group received the same conventional physical therapy program in addition to Sling exercise therapy (SET) and Whole-body vibration (WBV). Shoulder muscle strength was assessed for both groups by using Lafayette manual muscle tester before and after treatment.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Whole Body Vibration for Hemiparetic Cerebral Palsy
NCT05896111
Effect of Whole Body Vibration With Weighted Vest on Motor Function in Children With Spastic Diplegia
NCT05606926
WBV on Fascicle Lenght and Knee Joint Angle in CP
NCT06600984
Effect of Core Stability Excercises Program on Reaching in Children With Cerebral Palsy
NCT05316090
Whole Body Vibration in Rehabilitation of Spastic Cerebral Palsy
NCT06077136
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Conventional physical therapy program and Sling exercise therapy
Conventional physical therapy program and Sling exercise therapy
Conventional physical therapy program and Sling exercise therapy
The control group received a conventional physical therapy program in addition to sling exercise therapy (SET) for 60 minutes.
Whole body vibration
Whole body vibration
Whole body vibration
The study group received the same selected conventional physical therapy program in addition to sling exercise therapy (SET) given to the control group (for 30 minutes) besides whole body vibration (WBV) (for 30 minutes).
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Conventional physical therapy program and Sling exercise therapy
The control group received a conventional physical therapy program in addition to sling exercise therapy (SET) for 60 minutes.
Whole body vibration
The study group received the same selected conventional physical therapy program in addition to sling exercise therapy (SET) given to the control group (for 30 minutes) besides whole body vibration (WBV) (for 30 minutes).
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Aged from 4 to 9 years.
* Both gender participated.
* Having grade 1 and 1+ spasticity according to the Modified Ashworth Scale.
Exclusion Criteria
* Surgical or neurological disease of the upper limbs.
* Osteopenia or osteoporosis.
4 Years
9 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Cairo University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Mahmoud Usama Mahmoud Ahmed
Lecturer at Department of Physical Therapy for Paediatrics, Faculty of Physical Therapy, Cairo University, Cairo, Egypt.
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Faculty of Physical therapy, Cairo University
Giza, Office Post Cairo University Giza, Egypt
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
P.T.REC/012/004848
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.