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Status unknownNCT05042570IASTMUpdated Sep 13, 2021

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

An interventional study of Instrument Assisted Soft Tissue Mobilization and Stretching Exercises in Cerebral Palsy, sponsored by Istanbul University - Cerrahpasa. Status unknown at 1 site in Turkey. Open to participants aged 5 Years to 18 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2021-09-13.

Sponsored by Istanbul University - Cerrahpasa · Not applicable, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Sep 2021), so the status shown — last known as Not yet recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
39
Allocation
Randomized
Ages
5 Years to 18 Years
Sex
All
01

Study summary

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.

Read the detailed 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.

02

Conditions studied

  • Cerebral Palsy

Keywords

  • Cerebral Palsy
  • Instrument Assisted Soft Tissue Mobilization
  • Stretching Exercises
03

In context

Paralysis

751 studies on the registry are indexed under Paralysis; 134 are open to participants now.

This study's planned enrollment of 39 is above the median of 30 across 538 interventional studies indexed under Paralysis.

Browse Paralysis studies →

Lead sponsor

Istanbul University - Cerrahpasa is the lead sponsor of 680 studies on the registry; 208 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
5 Years to 18 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

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

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).
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Investigator, Outcomes assessor)
Enrollment
39 participants (estimated)

Study arms

  • Experimental
    Instrument Assisted Soft Tissue Mobilization

    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.

    Other: Instrument Assisted Soft Tissue Mobilization

  • Experimental
    Stretching Exercises

    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.

    Other: Stretching Exercises

  • Active comparator
    Control

    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.

    Other: Control Group / NDT program

Interventions

  • OtherInstrument Assisted Soft Tissue Mobilization

    * This technique will be performed using instruments of different sizes, shapes and treatment styles. * During the application, instruments will be applied to loosen the muscle tissue and fascia by gliding on the tissue at certain angles. * The muscle groups to be treated with IASTM are gastrocnemius, soleus and tibialis posterior. It will also be applied to the superficial and deep fascia. * The instrument will be sterilized before treatment. * IASTM treatment will be applied without damaging the tissue after massaging cream is applied to the muscle fibers with the instrument.

  • OtherStretching Exercises

    * The muscle groups to be applied stretching exercises are gastrocinemius, soleus and tibialis posterior. It will also be applied to the superficial and deep fascia. * 3 different functional stretching exercises will be applied; * With the hands supported on the wall and with the help of the physiotherapist, the affected extremity is behind the knee in full extension m. gastrocnemius stretching exercise, * With the hands supported on the wall and with the help of the physiotherapist, the knee is partially flexed, with the affected extremity behind. soleus stretching exercise, * It is a stretching exercise that will be applied by asking the patient to squat without lifting his heels, with the patient's hands supported by the physiotherapist.

  • OtherControl Group / NDT program

    * Efforts to eliminate tone disorders, * Sensory-perception-motor integrity development studies, * Activities aimed at facilitating movements in daily life, * Stretching and strengthening exercises due to muscle shortness and weakness, * Studies to increase lower and upper extremity functionality, * It will include the training of activities such as standing up, walking and balance.

06

What researchers measure

Primary outcomes

  1. Modified Ashworth Scale (MAS)

    In the evaluation of the presence of spasticity in patients with CP, the ankle plantar flexors will be based. It is recorded as an assessment of the resistance encountered while passively moving the limb at full range of motion. It is scored as 0, 1, 1+, 2, 3, 4. A value of 0 is the best score without muscle tone increase, while a value of 4 is when the extremity is in a rigid position. Modified Ashworth Scale (MAS) will be used to evaluate spasticity.

    Time frame: one month

  2. Pediatric Berg Balance Scale (PBBS)

    The Pediatric Berg Balance Scale, which is the version of the Berg Balance Scale designed for children by Franjoine et al., will be used to evaluate their functional balance in activities of daily living. The scale consists of 14 sections and each section is scored between 0-4; The highest score that can be obtained from the scale is 56.

    Time frame: one month

  3. Selective Motor Control Test (SMCT)

    Ankle dorsiflexion Selective Motor Control Test will be used in the evaluation of selective movements. This test evaluates the isolated dorsiflexion movement of the ankle and is evaluated between 0-4 according to the selectivity of the ankle dorsiflexion movement in the long sitting position.

    Time frame: one month

  4. Weight-Bearing Lunge Testi (WBLT)

    In order to measure the weight-bearing dorsiflexion ROM, the Weight-Bearing Lunge Test, which is positioned with support from the wall in the closed chain position, will be applied. An increase in ankle dorsiflexion angle will be considered as a positive result.

    Time frame: one month

07

Study locations

1 site
  • Istanbul University Cerrahpasa
    Istanbul, Turkey
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 13, 2021, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT05042570
Lead sponsor
Istanbul University - Cerrahpasa
Responsible party
Eren Avcıl (Principal Investigator, Istanbul University - Cerrahpasa) — Principal investigator
First posted
Sep 13, 2021
Start date
Nov 1, 2021 (estimated)
Primary completion
Jun 1, 2022 (estimated)
Completion
Dec 1, 2022 (estimated)
Last update
Sep 13, 2021

Study contacts

Eren Avcıl, Master
Contact
erenavcil@gmail.com
+9005320683378
İpek Yeldan, Prof
study director · Istanbul University - Cerrahpasa

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is status unknown, as verified in Sep 2021. You cannot join it, but the record below documents what was studied.

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