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
| Type | Name | Description |
|---|---|---|
| PROCEDURE | IASTM therapy in addition to the selected physical therapy program | The 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 |
| PROCEDURE | selected physical therapy program | The 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.