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Clinical Trials/NCT03005938
NCT03005938
Completed
Not Applicable

Influence of the Spinal Manipulation on Muscle Spasticity and Manual Dexterity in Children With Cerebral Palsy, Randomized Control Trial.

International Clinic of Rehabilitation, Ukraine1 site in 1 country85 target enrollmentSeptember 2016

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cerebral Palsy, Spastic
Sponsor
International Clinic of Rehabilitation, Ukraine
Enrollment
85
Locations
1
Primary Endpoint
Change of muscle spasticity after the intervention
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

The aim of the study is to evaluate a short term influence of the Spinal Manipulation (SM) on the wrist muscles spasticity and manual dexterity in children with spastic Cerebral Palsy.

Effect of SM and imitation of the SM has to be compared in the double-blinded randomized clinical trial.

Detailed Description

Muscle spasticity is an important clinical syndrome of Cerebral Palsy (CP) resulting from upper motor neuron lesion, and its reduction is a significant therapeutic target for optimizing motor performance. Investigator's recent study describes decrease in spasticity after SM in a group of children with CP. But that case series has no control group and the sample size was small so it does not prove the influence of the SM on the muscle spasticity. The purpose of the present study is to evaluate influence of the SM on muscle spasticity and on manual dexterity of the child with CP in a double-blind randomized clinical trial with two arms: SM (experimental group) and imitation of SM (control group). Children admitted to the International Clinic of Rehabilitation are selected according to inclusion-exclusion criteria and invited to participate. After getting the permission the baseline assessment is performed. Patients are allocated to the experimental or control group using stratified randomization. Medical doctor certified in Manual Therapy performs the intervention (SM in the experimental group and imitation in the control group) and in 15 minutes the second assessment is performed. Investigators, children and parents are blinded to group allocation.

Registry
clinicaltrials.gov
Start Date
September 2016
End Date
September 15, 2017
Last Updated
8 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
International Clinic of Rehabilitation, Ukraine
Responsible Party
Principal Investigator
Principal Investigator

Oleh Kachmar

Head of Innovative Technologies Department

International Clinic of Rehabilitation, Ukraine

Eligibility Criteria

Inclusion Criteria

  • Spastic uni-, bilateral Cerebral Palsy
  • Manual Ability classification level (MACS) - I-III level
  • Modified Ashworth scale (MAS) grade 1-3 in wrist or fingers flexors

Exclusion Criteria

  • Dyskinetic or ataxic syndrome
  • Less than 40 degrees of passive wrist extension with fingers extended
  • Botox injections in hand muscles during last year or recent antispastic drugs
  • Fracture in hand or forearm less than 6 month prior to examination
  • Uncooperative behavior, inability to understand and comply with instructions
  • Severe pain preventing the child from being able to complete examinations

Outcomes

Primary Outcomes

Change of muscle spasticity after the intervention

Time Frame: Baseline assesment and 15 min after intervention

Quantitative, instrumental spasticity measurement is preformed using the Neuroflexor device. It is measuring resistance to passive movements of the wrist performed with different speed and calculates components of muscle tone, separating spasticity as reflex phenomenon from resistance due to secondary changes of the muscles and tendons.

Secondary Outcomes

  • Change of manual dexterity after the intervention(Baseline assesment and 15 min after intervention)

Study Sites (1)

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