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Effect of FES Versus No FES intervention. A statistically significant between-group difference in activity in favor of FES was reported for all 3 studies, immediately after the intervention period. This difference represented a 30% to 32% greater increase in activity compared with no FES intervention. A follow-up measurement was reported for 1 study, but no data were reported.
Effect of FES Versus Activity Training. Both studies reported a statistically nonsignificant between-group difference in activity compared with activity training, immediately after the intervention period. One study included a follow-up measurement, but no data were reported
Full description
This study will be conducted at the Outpatient clinics, Faculty of Physical
Therapy Kafrelsheikh University to prove the effect of core stability exercises on standing , balance and gait in diplegic CP children.
the children will be randomly allocated by simple random method via choosing one of two wrapped cards representing the two treatment groups, which are: Group (A): will receive core stability exercises in addition to the designed physiotherapy program.
Group (B): will receive the designed physiotherapy program only . Inclusion criteria
Children will be included in the study if they fulfil the following criteria:
A medical diagnosis of diplegic CP made by paediatricians or pediatric neurologists.
Children with spasticity grades ranged from 1 to 1+ according to MAS.
Their age range from 4 to 10 years.
Children were level I or II on the Gross Motor Function Classifcation System (GMFCS) 5.No orthopedic surgeries.
Exclusion criteria
Children will be excluded from the study if:
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Inclusion and exclusion criteria
Inclusion Criteria:
A medical diagnosis of diplegic CP made by paediatricians or pediatric neurologists.
Children with spasticity grades ranged from 1 to 1+ according to MAS. 3. Their age range from 4 to 10 years.
Children were level I or II on the Gross Motor Function Classifcation System (GMFCS) 5.No orthopedic surgeries
Exclusion Criteria:
Primary purpose
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Interventional model
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40 participants in 2 patient groups
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Central trial contact
sara yousef elsebahy, phd
Data sourced from clinicaltrials.gov
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