Stroke Clinical Trial
Official title:
Impact of Transcranial Direct Current Stimulation (tDCS)on the Effects of Mental Practice and Modified Constraint-induced Movement Therapy (mCIMT)in the Rehabilitation of Chronic Stroke Patients
This study aims to evaluate systematically and controlled the effectiveness of mental practice techniques and modified constraint- induced movement therapy (mCIMT)in the treatment of post-stroke patients with motor deficit in the upper limb. As well as finding a protocol of transcranial direct current stimulation(tDCS)that will maximize the effects of the practice of mental image and mCIMT. To this end, the subjects included will be submitted to 12 therapy sessions with active or sham tDCS combined with at least one of the following techniques: conventional physiotherapy, mental practice technique or mCIMT
Eighty-four patients chronic post-stroke will be recruited to participate in the study.
After screening to check the eligibility criteria and giving informed consent, the patients
will be randomized into seven distinct groups (12 per group). All the patients will be
submitted to 12 therapeutic sessions that will occur with a frequency of three times a week.
Before, immediately after and 1 month after the beginning of the experimental sessions
patients will be submitted to an evaluation at each moment will be applied: (i) Fugl- Meyer
Scale, (ii) Motor Activity Log Scale, (iii ) Jebsen-Taylor hand functional test, (iv)
Independence Functional Measure (v) Box-Block Test, (vi) Dynamometry and (vii) Berg Balance
Scale.
In experimental sessions, the subjects always receive physiotherapy treatment with
conventional techniques, the protocol will follow the guidelines outlined in Clinical
Practice Guideline for physical therapy in stroke patients with the Royal Dutch Society for
Physical Therapy (2004). Besides physical therapy, the patient may be subjected to
transcranial direct current stimulation (tDCS) associated with the techniques of modified
constraint-induced movement therapy (mCIMT) or mental practice (MP).
tDCS protocol During tDCS sessions, the patients will be seated in a comfortable chair with
head and arm rests. Continuous direct current will be applied by clinical microcurrent
stimulator (Soterix, USA) using a pair of saline-soaked surface sponge electrodes (surface
35 cm2). For anodal and sham stimulation (the polarity refers always to the motor cortical
electrode), the anode electrode will be placed over primary motor cortex (M1; EEG 10/20
system) of the affected hemisphere and cathode above contralateral orbit. For cathodal tDCS,
the cathode will be positioned over M1 of the non-affected hemisphere and the anode was
placed above the contralateral orbit. For bi-hemispheric tDCS the anode electrode will be
placed over M1 of the affected hemisphere and the cathode over the M1 of the healthy
hemisphere. Transcranial direct current stimulation will be administered with a current
strength of 1 mA for 13 (anodal/bi-hemispheric tDCS) or 9 min (cathodal tDCS). Sham tDCS
will be performed by current flow for 30 s, a method shown to achieve a good level of
blinding mCIMT protocol The modified CIMT consisted of (i) complete immobilization of the
non-paretic upper limb and (ii) intensive training the paretic upper limb and will be
administered by a trained therapist, who was not involved in the pre-post evaluations.
Continuously for six hours daily over a period of four weeks, including weekend, all
patients will be remained with complete immobilization of the non paretic upper limb. For
this, an arm sling with the shoulder in adduction and internal rotation, elbow flexed at
90º, wrist and fingers in neutral position, made specifically for each patient will be used.
They will be advised to use the restriction during their daily activities and instructed to
remove it every hour for 10 minutes to perform stretching, which has been previously taught
by the researchers to avoid functional deterioration caused by disuse. All muscle groups of
the upper extremity will be stretched. A guide with instructions of the stretching will be
distributed to patients. The patients will be instructed to take the immobilization on every
day at same hour the tDCS sessions. In addition, the patients will be allowed to take the
arm sling off during activities in which safety would be compromised, such as toileting,
dressing, and bathing.
For intensive training the paretic upper limb, the patients will attend a gross motor and
fine motor activities program performed for 1 hour per day, three times per week. Each task
was performed for 2-3 minutes and the rest interval between tasks will be determined for
each subject in order to avoid fatigue and excessive tiredness. The tasks will be
progressively adapted by increasing speed or accuracy to allow improvement of patient
performance. All tasks will be done with subjects sitting on a chair with standard
dimensions and performed on support table. During training sessions, the patients will
remain with the non-paretic arm immobilized.
Mental practice protocol Prior to experimental sessions, the mental capacity of subjects to
learn the imagery techniques will be tested by the Kinesthetic and Visual Imagery
Questionnaire and a chronometric test. The Kinesthetic and Visual Imagery Questionnaire is
an imagery assessment tool comprised of 10 items, each scored on a five-point ordinal scale,
including the image clarity (visual dimension) and the sensations intensity (kinesthetic
dimension) of body movements. Each item describes an action: (i) neck flexion/extension,
(ii) shoulder shrugging, (iii) forward trunk flexion, (iv) forward shoulder flexion, (v)
elbow flexion, (vi) thumb to finger tips, (vii) knee extension, (viii) hip abduction, (ix)
foot external rotation, and (x) foot tapping. Subjects physically execute each movement and
immediately afterwards imagine performing the same movement. A score of 5 corresponds to the
highest clarity/intensity, and a score of 1 corresponds to the lowest clarity/ intensity
(for a review, see Malouin et al., 2007). The Kinesthetic and Visual Imagery Questionnaire
scores allowed the researcher to assess each participant's abilities and decide whether the
subject was a suitable candidate for MP. Comparing actual and imagined movement times, the
chronometric test determined the motor imagery ability of participants.
The mental practice will consist of motor imagination of tasks. These tasks will consist of
action for the patient to imagine themselves, with the greatest wealth of detail possible,
performing motor activities with the hemiparetic upper limb, such as the movement of the
touching thumb on each other's toes hand, or even the movement of bringing a cup towards his
mouth. The technique of mental practice will be applied at the same time of the tDCS.
;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Treatment
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