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Effect of IASTM in Children With Diplegia

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07289386
Enrollment
30
Registered
2025-12-17
Start date
2024-03-01
Completion date
2024-12-01
Last updated
2025-12-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cerebral Palsy (CP)

Keywords

Cerebral palsy, Gait

Brief 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.

Interventions

PROCEDUREIASTM 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

PROCEDUREselected 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

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Caregiver)

Eligibility

Sex/Gender
ALL
Age
5 Years to 8 Years
Healthy volunteers
No

Inclusion criteria

* Children aged from 5 to 8 years old. * spasticity ranged from 1 to 1+, according to Modified Ashworth Scale * Children at level II according to Gross Motor Function Classification System * They achieved independent walking with or without assistive device * able to follow instructions and understand commands.

Exclusion criteria

* Fixed muscle contractures or fixed bone deformities in the lower limb. * Botox injection for the last six months. * Orthopedic surgeries for the last year. * Children with infectious diseases. * Skin infection, seizures, and any lower limb soft tissue injury.

Design outcomes

Primary

MeasureTime frameDescription
Active range of motionsix weeksmeasured by 2D gait analysis

Secondary

MeasureTime frameDescription
passive range of motionsix weeksmeasured by a digital goniometer

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026