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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05331703
Other study ID # P.T.REC/012/0035A342
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date December 22, 2022
Est. completion date December 22, 2023

Study information

Verified date April 2022
Source October 6 University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Previous research has demonstrated balance deficits ranging from 28%-43% depending on the nature of the balance task in individuals with CP compared to controls (Kenis-Coskun et al., 2016). As balance is critical for underlying normal movement, improvements in static and dynamic balance are important goals in rehabilitation for ambulatory children with CP (Saether et al., 2013). Balance deficits are among the symptoms that having a more profound impact on motor function and quality of life inn with CP children (Lai et al., 2017). Poor balance reduces the ability to perform gait-related activities and increases the risk of falling, which, in turn, limits participation in daily activities, including sports and physical activities (Usuba et al., 2015).


Recruitment information / eligibility

Status Recruiting
Enrollment 40
Est. completion date December 22, 2023
Est. primary completion date March 22, 2023
Accepts healthy volunteers No
Gender All
Age group 6 Years to 10 Years
Eligibility Inclusion Criteria: - Their ages will range from 6 to 10 years old. - The degree of spasticity will range from 1+ to 2 grades according to Modified Ashworth scale (NUMANO and Günel, 2011) (Appendix II). - They will be on level I and II on Gross Motor Function Classification System (GMFCS) (Palisano et al., 2008) (Appendix III). - Their heights will be one meter or more. - They will be able to follow the verbal commands or instructions. Exclusion Criteria: - Severe visual or auditory problems. - Epilepsy. - History of surgical interference in lower limbs. - Botulinum toxin injections of the lower limbs during the previous six

Study Design


Related Conditions & MeSH terms


Intervention

Other:
designed physical therapy program in addition to program of virtual reality.
physical therapy program in addition to program of virtual reality.
designed physical therapy program in addition to program of mirror therapy.
physical therapy program in addition to program of mirror therapy.

Locations

Country Name City State
Egypt Emad Eldin Cairo October

Sponsors (1)

Lead Sponsor Collaborator
October 6 University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Biodex balance system The Biodex balance System to measures postural stability under dynamic stress. 3 months
Primary Hand held dynamometer The hand held dynamometry to measure muscle strength of non-disabled children 3 months
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