The Effect of Instrument Assisted Soft Tissue Mobilization and Stretching Exercises in Cerebral Palsy (IASTM)
Cerebral Palsy
About this trial
This is an interventional treatment trial for Cerebral Palsy focused on measuring Cerebral Palsy, Instrument Assisted Soft Tissue Mobilization, Stretching Exercises
Eligibility Criteria
Inclusion Criteria:
- Having been diagnosed with Unilateral Spastic Type Cerebral Palsy by the health committee report,
- Level I or II according to GMFCS,
- Being between the ages of 5-18,
- No Botulinum Toxin (Botox) injection in the last 6 months,
- Not using any medication that may affect muscle tone,
- Passive ankle dorsiflexion + 10o and passive plantar flexion -25o,
- Families and children agree to participate voluntarily in the study.
Exclusion Criteria:
- Having undergone any lower extremity surgery,
- Tone in plantar flexors is level IV according to MAS,
- Presence of advanced contracture in the ankle,
- Presence of any diagnosed cardiac or orthopedic disorder that may prevent the application of the treatment,
- Hearing or vision problems,
- Having a history of epileptic attacks,
- Not having the ability to adapt to exercises (cases with the phrase "Mental Retarde" according to the health report).
Sites / Locations
- Istanbul University Cerrahpasa
Arms of the Study
Arm 1
Arm 2
Arm 3
Experimental
Experimental
Active Comparator
Instrument Assisted Soft Tissue Mobilization
Stretching Exercises
Control
Group 1 (n=13): Each session will consist of 40 minutes. An additional 10 minutes of IASTM will be performed to the 30-minute NDT program.
Group 2 (n=13): Each session will consist of 40 minutes. In addition to the NDT program applied for 30 minutes, 10 minutes of Stretching Exercises will be performed.
Group 3 (n=13): Each session will consist of 40 minutes. There will be no additional application to the NDT program, which is applied for 40 minutes, and it will be included as a control group in the study.