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Efficacy of a Long Term, High Intensity and Long Time Stretch Training Program on Viscoelasticity Plantarflexors Muscle in Children With Cerebral Palsy (CP).

Efficacy of a Long Term, High Intensity and Long Time Stretch Training Program on Viscoelasticity Plantarflexors Muscle in Children With Cerebral Palsy (CP).

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03565172
Acronym
LONGSTRETCH PC
Enrollment
1
Registered
2018-06-21
Start date
2018-07-02
Completion date
2018-07-26
Last updated
2022-08-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cerebral Palsy, Spastic, Children, Only

Keywords

cerebral palsy, stretching, isokinetic dynamometer, ultrasound, ankle, children

Brief summary

Children with cerebral palsy present early in the childhood altered muscular properties, as soon as structural or stiffness. In the gastrocnemius muscle, altered muscular properties are characterized by short muscle belly length and increased stiffness which contribute to contracture and limiting joint range of motion.

Detailed description

This study assess efficacy of a long term stretching program of plantarflexors muscle on their viscoelasticity properties and maximal dorsiflexion angle gain. Stretching program is characterized by 3 phases: baseline, intervention and follow-up.

Interventions

DIAGNOSTIC_TESTisokinetic dynamometer with ultrasound

children are lying prone on a isokinetic dynamometer with ultrasound which stretches spastic and paretic plantarflexors muscles very slowly until maximal torque tolerated. The parameters can be measured.

the discomfort level will be measured by Visual Analog Scale (VAS) completed by children. 0 = no discomfort and 10 = maximum discomfort

DIAGNOSTIC_TESTStretching

the ankle of children will be mobilized for 5 minutes (first two weeks) to 10 minutes (last two weeks).

Sponsors

Centre Hospitalier Universitaire de Saint Etienne
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE

Intervention model description

The methodology used is : Single Case Experimental Design (SCED).

Eligibility

Sex/Gender
ALL
Age
8 Years to 16 Years
Healthy volunteers
No

Inclusion criteria

* Children aged 8 to 16 years * Children diagnosed spastic cerebral palsy * Children with decrease maximal dorsiflexion angle under +5° in the last four weeks * Children who don't understand instructions

Exclusion criteria

* Children who had damage orthopedics or surgical operation contraindicating realization of the experimental protocol * Hospitalization incompatible with the progress of the protocol. * Children who had botulinum injection, extensions casts or the implementation of new equipment (night or day orthosis) for less than three months or the progress of the protocol. * Children having analgesic treatment in progress

Design outcomes

Primary

MeasureTime frameDescription
slope of the torque-angle curveup to 12 weeksAnalysis of the slope of the torque-angle curve in Nm/°. It is measured by isokinetic dynamometer with ultrasound.

Secondary

MeasureTime frameDescription
Maximal dorsiflexion angleup to 12 weeksAnalysis of the maximal dorsiflexion angle in degrees. It is measured by isokinetic dynamometer with ultrasound.
Slope of the torque- MyoTendinous Junction (MTJ) displacementup to 12 weeksAnalysis of the Slope of the torque- MyoTendinous Junction (MTJ) displacement in cm/°. It is measured by isokinetic dynamometer with ultrasound.
MyoTendinous Junction (MTJ) displacement of muscle triceps suralup to 12 weeksAnalysis of the MyoTendinous Junction (MTJ) displacement of muscle triceps sural in cm. It is measured by isokinetic dynamometer with ultrasound.
muscle triceps sural, muscle body of the medial gastrocnemius muscle and Achilles tendonup to 12 weeksCorrelation of the length of Musculo-Tendinous Unit (MTU) of muscle triceps sural, muscle body of the medial gastrocnemius muscle and Achilles tendon. It is measured by isokinetic dynamometer with ultrasound.
discomfort levelup to 12 weeksAnalysis of the discomfort level. It is measured by Visual Analog Scale (VAS) completed by children. 0 = no discomfort and 10 = maximum discomfort

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026