Efficacy of Extracorporeal Shock Wave Therapy in Children With Cerebral Palsy

Sponsor
Kocaeli University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT06128616
Collaborator
(none)
40
2
10

Study Details

Study Description

Brief Summary

Spastic plantar and palmar flexion deformities are very common in children with cerebral palsy (CP). These deformities usually involve spasticity of the plantar or palmar muscle complexes, weakness of the antagonist dorsiflexor muscles of the ankle or wrist, and also involve soft tissue/muscle contractures and require a multimodal treatment approach. Physical therapy (PT), occupational therapy (OT), serial casting (SC), and botulinum toxin A (BoNT-A) injections had shown positive results in both of these deformities. Recent systematic reviews and meta-analyses showed that extracorporeal shock wave therapy (ESWT) is effective in reducing spasticity, pain intensity, and increasing range of motion and motor function when combined with PT or BoNT-A injections in neurological conditions like stroke, CP, multiple sclerosis. ESWT can be a complimentary therapy to obtain an earlier efficacy, better efficacy, a sustained effect for a longer period, and less adverse events. The objective of this study was to show the effects of ESWT when combined with intermittent SC, BoNT-A injections and PT or OT on spasticity, passive range of motion (pROM) of children with CP having spastic equinus foot deformity or wrist palmar flexion deformity.

Condition or Disease Intervention/Treatment Phase
  • Device: ESWT
  • Drug: Botulinum Toxin Type A
  • Other: Serial Casting
  • Behavioral: Physical Therapy
  • Behavioral: Occupational Therapy
Phase 3

Detailed Description

Spasticity is one of the most common motor disorder which may slowly cause soft tissue contractures in children with CP. Spastic plantar and palmar flexion deformities are very common in children with CP. These deformities usually involve spasticity of the plantar or palmar muscle complexes, weakness of the antagonist dorsiflexor muscles of the ankle or wrist, and also involve soft tissue/muscle contractures. PT, OT, SC, and BoNT-A injections had shown positive results in both of these deformities. Skin irritation or breakdown, painful episodes, oedema, tendonitis, weakness, stiffness are some of the side effects reported after SC. Moreover casting especially when prolonged might complicate activities of daily living for instance by increasing the risk of falls or causing problems in bathing. Recent evidence from literature favors early, goal oriented, activity based, intensive, repetitive motor trainings in enriched environments to optimize neuroplasticity in children with CP. Prolonged SC might also interfere with these activity based, intensive rehabilitation options for upper extremity. In order to overcome the issues with patient compliance, side effects and combined treatment options an intermittent SC model was developed and used both for children with CP presenting equines foot deformity or palmar flexion deformity. Combined management of intermittent SC, and BoNT-A injections had shown better results compared to either treatment alone in both of these deformities. Recent systematic reviews and meta-analyses showed that ESWT is effective in reducing spasticity, pain intensity, and increasing range of motion and motor function when combined with PT or BoNT-A injections in neurological conditions like stroke, CP, multiple sclerosis. ESWT can be a complementary therapy to obtain an earlier efficacy, better efficacy, a sustained effect for a longer period, and less adverse events.

The objective of this study was to show the effects of ESWT when combined with intermittent SC, BoNT-A injections and PT or OT on spasticity, passive range of motion (pROM) of children with CP having spastic equinus foot deformity or wrist palmar flexion deformity.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
40 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Efficacy of Extracorporeal Shock Wave Therapy Integrated to Combined Treatment of Botulinum Toxin A and Serial Casting in Children With Cerebral Palsy
Anticipated Study Start Date :
Nov 1, 2023
Anticipated Primary Completion Date :
Jun 1, 2024
Anticipated Study Completion Date :
Sep 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: ESWT Group

Patients treated by BoNT-A, intermittent SC and ESWT, whom received either PT or OT

Device: ESWT
Extracorporeal Shock Wave Therapy

Drug: Botulinum Toxin Type A
Botulinum Toxin Type A
Other Names:
  • Botox
  • Other: Serial Casting
    Serial Casting

    Behavioral: Physical Therapy
    Physical Therapy

    Behavioral: Occupational Therapy
    Occupational Therapy

    Active Comparator: Control Group

    Patients treated by BoNT-A, and intermittent SC, whom received either PT or OT

    Drug: Botulinum Toxin Type A
    Botulinum Toxin Type A
    Other Names:
  • Botox
  • Other: Serial Casting
    Serial Casting

    Behavioral: Physical Therapy
    Physical Therapy

    Behavioral: Occupational Therapy
    Occupational Therapy

    Outcome Measures

    Primary Outcome Measures

    1. Mean change from baseline Tardieu XV3 angle [Post-treatment weeks 4-6]

      Spasticity measurement

    2. Mean change from baseline passive range of movement [Post-treatment weeks 12-20]

      Soft tissue contracture measurement

    Secondary Outcome Measures

    1. Goal Attainment Scale-Light [Post-treatment weeks 4-12-20]

      Attainment of treatment goals 5 point scale ranging from -2 to 2, higher score representing better outcome

    2. Faces Pain Scale [Post-treatment weeks 4-12-20]

      Assessment of pain by a visual 6 point scale ranging from 0 to 10, 0 representing no pain, 10 representing most excruciating pain

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    3 Years to 17 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Having a diagnosis of CP according to Rosenbaum criteria, presenting plantar or palmar flexion deformity, having a Modified Ashworth Scale score of 3 in plantar or palmar flexor muscle groups, being scheduled for BoNT-A treatment, intermittent serial casting and physical or occupational therapy
    Exclusion Criteria:
    • Having cognitive dysfunction, having a history of orthopedic surgery, presenting significant dystonia, having vascular disease, fracture, or dislocation

    Contacts and Locations

    Locations

    No locations specified.

    Sponsors and Collaborators

    • Kocaeli University

    Investigators

    • Principal Investigator: Nigar Dursun, MD, Kocaeli Universitesi

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Nigar Dursun, Professor, Kocaeli University
    ClinicalTrials.gov Identifier:
    NCT06128616
    Other Study ID Numbers:
    • KAEK/16.bI.06
    First Posted:
    Nov 13, 2023
    Last Update Posted:
    Nov 18, 2023
    Last Verified:
    Nov 1, 2023
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Product Manufactured in and Exported from the U.S.:
    No
    Keywords provided by Nigar Dursun, Professor, Kocaeli University
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Nov 18, 2023