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Clinical Trials/NCT02579291
NCT02579291
Completed
Not Applicable

Changes in Spasticity, Motor Function and Stabilometry After Dry Needling of the Tibialis Posterior Muscle in Post-stroke Patients

Universidad Rey Juan Carlos1 site in 1 country30 target enrollmentOctober 2015
ConditionsStroke

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Stroke
Sponsor
Universidad Rey Juan Carlos
Enrollment
30
Locations
1
Primary Endpoint
Changes in spasticity before and 10 minutes after the intervention
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

Individuals who had experience a stroke usually suffer from spasticity at medium and long-terms. The presence of spasticity in the lower extremity implies several impairments for standing and walking inducing high disability. A recent study has proposed the use of dry needling for improving spasticity in the lower extremity. No study has investigated the effects of deep dry needling inserted into spastic musculature in stabilometry and moto function in patients who had experience a stroke. A randomized controlled trial investigating the effects of the inclusion of deep dry needling into a Bobath interventional program on spasticity, motor function and balance (stabilometry) in individuals who had experience a stroke

Registry
clinicaltrials.gov
Start Date
October 2015
End Date
May 2016
Last Updated
9 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

César Fernández-de-las-Peñas

Head Division

Universidad Rey Juan Carlos

Eligibility Criteria

Inclusion Criteria

  • First-ever unilateral stroke;
  • hemiplegia resulting from stroke;
  • unilateral equinovarus gait with independent walk;
  • able to ambulate without supporting devices

Exclusion Criteria

  • recurrent stroke;
  • previous treatment with nerve blocks, motor point injections with neurolytic agents for spasticity at any time, or with BTX-A in the previous 6 months
  • not independent in the basic activities of daily living
  • cognitive deficits;
  • progressive or severe neurologic diseases;
  • fear to needles;
  • any contraindication for dry needling

Outcomes

Primary Outcomes

Changes in spasticity before and 10 minutes after the intervention

Time Frame: Baseline and immediate after the intervention

Spasticity in the affected ankle joint will be evaluated with the Modified Modified Ashworth Scale (MMAS). The examiner passively will move the ankle in dorsal-flexion direction, back and forth at least 5 times and will evaluate the degree of resistance to the movement on a scale from 0-4.

Secondary Outcomes

  • Changes in stabilometry outcomes before and 10 minutes after the intervention(Baseline and immediate after the intervention)
  • Changes in motor function before and 10 minutes after the intervention(Baseline and immediate after the intervention)

Study Sites (1)

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