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Clinical Trials/NCT03329807
NCT03329807
Unknown
Not Applicable

Effects of Transcranial Magnetic Stimulation Associated to Sensory Therapy for Treatment of Motor Function of Upper Limb of Stroke Patients

Universidade Federal de Pernambuco2 sites in 1 country40 target enrollmentJuly 20, 2017
ConditionsStroke

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Stroke
Sponsor
Universidade Federal de Pernambuco
Enrollment
40
Locations
2
Primary Endpoint
change from Fugl-Meyer assessment
Last Updated
8 years ago

Overview

Brief Summary

The aim of this research will be to investigate in stroke patients whether upper limb motor function can be maximized in response to sensory stimulation by comparing protocols for the application of Transcranial Magnetic Stimulation (rTMS) in the cortical region of S1 and Sensory Therapy in the upper limb paretic. Patients will be randomly and randomly allocated into four groups, Group 1 (G1) composed of individuals who will receive the protocol for the application of rTMS in the ipsilateral S1 cortex and fictitious sensory therapy in the paretic upper limb; Group 2 (G2) subjects will receive protocol of Sensory Therapy in the upper limb ethical and application of fictitious rTMS in the ipsilesional S1 cortex; Group 3 (G3): application of the protocol of application of rTMS in the ipsilateral S1 cortex associated with Sensory Therapy in the upper limb paretic and, G4 (GSHAM) control group in which fictitious rTMS will be performed and fictitious Sensory Therapy in the paretic upper limb).

Registry
clinicaltrials.gov
Start Date
July 20, 2017
End Date
August 30, 2019
Last Updated
8 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Kátia Monte-Silva

Clinical Professor; PHD

Universidade Federal de Pernambuco

Eligibility Criteria

Inclusion Criteria

  • diagnosis of ischemic or hemorrhagic stroke proven by means of computed tomography or magnetic resonance imaging,
  • absence of cognitive deficits (evaluated by Mini Mental State Examination, score ≥ 20 - FOLSTEIN 1975);
  • partially preserved motor functions (evaluated by the Fugl-Meyer Scale, score between 14 and 60, due to the necessary movements to be performed during the intervention);
  • partially preserved sensorial (evaluated by the Fugl-Meyer Scale, score between 2 and 10 in the sensorial item , Indicating subjects with sensorial alterations but without extinction of the sensation) (MAKI, QUAGLIATO, CACHO, et al., 2006);
  • patients who, through exposure to electric current by TENS, perceive the electrical stimulation in the palm, back of the hand and ventral forearm will be included.

Exclusion Criteria

  • clinical evidence of multiple brain lesions or other associated neurological diseases;
  • peripheral neuropathies;
  • fibromyalgia;
  • rheumatoid arthritis;
  • other upper and lower motor neuron pathologies;
  • sensitizing skin diseases;
  • history of psychiatric illnesses including drug and alcohol abuse;
  • traumato-orthopedic deformities installed in upper limbs;
  • those who are performing some rehabilitation treatment during the collection (Physiotherapy and / or Occupational Therapy) will not participate in the research.
  • In addition, for the application of rTMS:

Outcomes

Primary Outcomes

change from Fugl-Meyer assessment

Time Frame: baseline; post-intervention. The re-evaluation will be in the eleventh session on the fourth week.

The Fugl-Meyer assessment (FMA) is considered the gold standard for evaluating the motor function recovery. It is designed to assess motor functioning, balance, sensation, and joint functioning. It is applied within clinical and in research contexts to determine the disease severity, describe motor recovery, and plan and assess interventions. In the present study, the 33-item of the UL section was employed. The items are rated on 3-point ordinal scale, as follows: 0= unable to perform; 1= partial ability to perform; and 2= near normal ability to perform. The UL subscale evaluates motor function recovery in six domains: flexor and extensor synergies, non-synergic movements, wrist and hand movements, and coordination and speed

change from The Jebsen-Taylor

Time Frame: baseline; post-intervention. The re-evaluation will be in the eleventh session on the fourth week

The Jebsen-Taylor manual function test will be used to assess motor function . This test consists of seven tasks: writing a sentence, turning cards and small common objects, feeding simulation, stacking chips, moving large light objects and large heavy objects. Each task will be timed by the Timer, the test will be done bilaterally, always starting with the healthy hand. Patient errors will also be recorded in numbers in case of misspelled words, for example; Changes in strategy to turn cards; Dropping small objects, beans, checkers or cans.

change from The Motor Activity Long (MAL)

Time Frame: baseline; post-intervention. The re-evaluation will be in the eleventh session on the fourth week.

The Motor Activity Long (MAL) test, validated and adapted to the Portuguese language, takes into account the patient's "learning to not use" upper limb (MAS) and the functional reacquisition of arm and hand skills in daily activities. The test has two ordinal scales, each with six points for the graduation of activities: one scale relates to quantity and the other to the quality of MSA use. On the quantitative scale, scores range from zero (do not use the MSA) to five (use the MSA the same way you used before the stroke). On the qualitative scale, the score also ranges from zero (the MSA is not used at all for the activity) to five (your ability to use the MSA is as good as it was before the stroke). In this qualitative section the score can have intermediate scores as 0.5 or 1.5.

change from The Box and Blocks test (TBB)

Time Frame: baseline; post-intervention. The re-evaluation will be in the eleventh session on the fourth week.

The Box and Blocks test (TBB) is an instrument commonly used in manual dexterity investigations, it can be used in post-stroke patients. At TBB, one hundred and fifty blocks of 2.5-cm wood are arranged in a wooden box in many different orientations. The place in wood has a partition of 15.2 cm of height dividing the space in two. The patient is instructed to carry as many blocks as possible from one space to another. The subject's score is equal to the number of those blocks transported in a partition in one minute. The more blocks transported the better the patient's manual dexterity

Secondary Outcomes

  • change from Functional Independence(baseline; post-intervention. The re-evaluation will be in the eleventh session on the fourth week.)
  • change from Thermography(baseline; post-intervention. The re-evaluation will be in the eleventh session on the fourth week.)
  • change from cortical excitability(baseline; post-intervention. The re-evaluation will be in the eleventh session on the fourth week.)
  • change from Upper limb cutaneous sensitivity(baseline; post-intervention. The re-evaluation will be in the eleventh session on the fourth week.)

Study Sites (2)

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