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Clinical Trials/NCT02690493
NCT02690493
Completed
Phase 2

The Efficacy of an Acupuncture Protocol and Use of Taping in the Treatment of Spastic Upper Limb After Stroke

Fernanda Cechetti1 site in 1 country12 target enrollmentJanuary 2015

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Stroke
Sponsor
Fernanda Cechetti
Enrollment
12
Locations
1
Primary Endpoint
The change of level of spasticity of upper limb after 12 sessions of intervention, assessed using the Modified Ashworth Scale
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

The purpose of this study is to determine whether acupuncture and taping are effective in the treatment of spastic upper limb after stroke.

Detailed Description

Acupuncture and taping have emerged as treatment alternatives for many diseases with positive and satisfactory results. Thus, acupuncture seeks to balance all physiological systems, using specific points on the body where needles are inserted. In turn, the use of taping is associated to various benefits such as improved blood and lymphatic function. In addition, it assists in the correction of muscle function and in the decrease of pain for neurological suppression. The constant afferent mechanical and somatosensory stimuli are perceived in cortical level and may produce motor unit recruitment and contribute to neuroplasticity of the nervous system. Thus, this research aims to analyze the effects of Acupuncture associated with Functional Taping on patients' upper limb with chronic hemiparesis after Stroke through a prospective, randomized intervention. Seventy-five patients will be evaluated before and after intervention with Acupuncture and / or Function Taping, divided into three groups (Acupuncture, Functional Taping and Acupuncture plus Functional Taping). The evaluation will consist of Isokinetic, Mini-Mental State Examination, Modified Ashworth Scale, Motor Activity Log, Wolf Motor Function Test and Visual Analog Scale of Pain. The results will be analyzed and presented descriptively, as of statistical comparisons of pre- and post-treatment and the relationship between the groups.

Registry
clinicaltrials.gov
Start Date
January 2015
End Date
December 2015
Last Updated
10 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Fernanda Cechetti
Responsible Party
Sponsor Investigator
Principal Investigator

Fernanda Cechetti

Clinical Professor

Federal University of Health Science of Porto Alegre

Eligibility Criteria

Inclusion Criteria

  • Patients with stroke diagnosis for at least six (06) months, who present hemiparesis in upper limb;
  • To accept participate in the study by signing theTerms of Consent;
  • Do not have any cognitive impairment.

Exclusion Criteria

  • Do not follow the inclusion criteria;
  • To present shoulder subluxation or dislocation, shoulder pain syndrome or amputations (with or without the use of aids);
  • To present any allergic reaction due to use of bandage and/or do not adapt to treatment with needles.

Outcomes

Primary Outcomes

The change of level of spasticity of upper limb after 12 sessions of intervention, assessed using the Modified Ashworth Scale

Time Frame: Immediately before the first session of intervention and 2 days after the last (12th) session of intervention.

Modified Ashworth Scale

Secondary Outcomes

  • The change of frequency of movement of upper limb after 12 sessions of intervention(Immediately before the first session of intervention and 2 days after the last (12th) session of intervention.)
  • The change of quality of movement of upper limb after 12 sessions of intervention(Immediately before the first session of intervention and 2 days after the last (12th) session of intervention.)
  • The change of amplitude of movement after 12 sessions of intervention, assessed using Manual Goniometer(Immediately before the first session of intervention and 2 days after the last (12th) session of intervention.)
  • The change of level of pain in upper limb after 12 sessions of intervention, assessed using Visual Analogue Scale(Immediately before the first session of intervention and 2 days after the last (12th) session of intervention.)
  • The change of functionality of upper limb after 12 sessions of intervention, assessed using the Wolf Motor Function Test(Immediately before the first session of intervention and 2 days after the last (12th) session of intervention.)

Study Sites (1)

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