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The Effect of Instrument Assisted Soft Tissue Mobilization and Stretching Exercises in Cerebral Palsy (IASTM)

I

Istanbul University - Cerrahpasa (IUC)

Status

Unknown

Conditions

Cerebral Palsy

Treatments

Other: Control Group / NDT program
Other: Instrument Assisted Soft Tissue Mobilization
Other: Stretching Exercises

Study type

Interventional

Funder types

Other

Identifiers

NCT05042570
EAvcil2

Details and patient eligibility

About

The aim of the study; To investigate the effects of Instrument Assisted Soft Tissue Mobilizations and Stretching Exercises on flexibility, spasticity, balance and functional mobility in patients with CP.

Full description

Various intervention studies; reported positive results with EDYDM after carpal tunnel syndrome, myofascial trigger point, chronic low back pain, nonspecific thoracic spine pain, ankle instability, mastectomy and total joint arthroplasty. Observational studies have shown positive results in improving posterior shoulder range of motion, hip, knee, and ankle ROM.

There is no study in the literature with EDYDM in patients with CP. Many of the problems in which EDDM is applied for fascia and muscle mobilization in different diseases are also seen in patients with CP. In current rehabilitation methods, Stretching Exercises are applied for muscle and fascia shortening. The advantages of the applications over each other are unknown. Our study is planned as a study with high original value as it is the first study to be conducted using EDYDM in cases with CP. In our study, the effectiveness of EDYDM treatment, which will increase the effectiveness of stretching exercises in CP or can be an alternative treatment approach in cases with CP, will be compared with Stretching Exercises.

Enrollment

39 estimated patients

Sex

All

Ages

5 to 18 years old

Volunteers

Accepts Healthy Volunteers

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).

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

39 participants in 3 patient groups

Instrument Assisted Soft Tissue Mobilization
Experimental group
Description:
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.
Treatment:
Other: Instrument Assisted Soft Tissue Mobilization
Stretching Exercises
Experimental group
Description:
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.
Treatment:
Other: Stretching Exercises
Control
Active Comparator group
Description:
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.
Treatment:
Other: Control Group / NDT program

Trial contacts and locations

1

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Central trial contact

Eren Avcıl, Master

Data sourced from clinicaltrials.gov

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