Clinical Trials Directory

Trials / Completed

CompletedNCT07289386

Effect of IASTM in Children With Diplegia

Effect of Instrument-assisted Soft Tissue Mobilization on Gait in Children With Spastic Diplegia

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
30 (actual)
Sponsor
Cairo University · Academic / Other
Sex
All
Age
5 Years – 8 Years
Healthy volunteers
Not accepted

Summary

The aim was to evaluate the effect of using IASTM on passive ROM of the lower limbs and joint angles during gait in children with spastic diplegic CP. Methods: Thirty children with diplegic CP were randomly divided into 2 groups: a control group (which received a selected physical therapy program) and the study group (which received IASTM therapy in addition to the selected physical therapy program). They were treated three times weekly for six weeks. Passive ROM and active ROM during gait were assessed using a digital goniometer and Kinovea analysis software, respectively, before and after the proposed treatment period.

Detailed description

Methods: Thirty children with diplegic CP were randomly divided into 2 groups: a control group (which received a selected physical therapy program) and the study group (which received IASTM therapy in addition to the selected physical therapy program). They were treated three times weekly for six weeks. Passive ROM and active ROM during gait were assessed using a digital goniometer and Kinovea analysis software, respectively, before and after the proposed treatment period.

Conditions

Interventions

TypeNameDescription
PROCEDUREIASTM therapy in addition to the selected physical therapy programThe designed IASTM therapy was applied for 8-10 minutes per session, three times per week (every other day), for six successive weeks in addition to the selected physical therapy program was applied for one hour per session, three times per week (every other day), for six successive weeks
PROCEDUREselected physical therapy programThe selected physical therapy program was applied for one hour per session, three times per week (every other day), for six successive weeks

Timeline

Start date
2024-03-01
Primary completion
2024-12-01
Completion
2024-12-01
First posted
2025-12-17
Last updated
2025-12-17

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT07289386. Inclusion in this directory is not an endorsement.