Effects of Transcranial Direct Current Electrical Stimulation on the Recovery of Ideomotor Apraxia of the Upper Limbs

Effects of Transcranial Direct Current Electrical Stimulation (tDCS) on the Recovery of Ideomotor Apraxia of the Upper Limbs in Patients With Acute Stroke

Limbs apraxia is a motor disorder whose characteristic is the inability or difficulty to perform intentional movements of the limbs (gestures), most frequently involving the upper limbs. Recent literature indicated promising effects of transcranial direct current stimulation (tDCS) in the recovery of limbs apraxia, showing that, in stroke patients, excitatory anodal tDCS over left inferior parietal lobe (IPL) may improve limb apraxia. Despite this encouraging evidence, the need for larger well powered and sham-controlled clinical trials has also been identified. For these reasons, the objective of this study is to investigate the effects of tDCS application on the left posterior parietal cortex, associated with the treatment for apraxia made by Smania et al. in 2000, on the recovery of the upper limbs ideomotor apraxia in patients with left brain lesion of vascular origin.

Study Overview

• Status: Recruiting
• Conditions: Apraxia, Ideomotor
• Intervention / Treatment: Device: transcranial Direct Current Stimulation (tDCS); Device: Behavioural; Device: Sham stimulation (sham-tDCS)

• Study Type: Interventional
• Enrollment (Estimated): 20
• Phase: Not Applicable

Contacts and Locations

• Study Contact: Name: LAURA ABBRUZZESE; Phone Number: 3473333750; Email: laura.abbruzzese@libero.it
• Study Contact Backup: Name: CRISTIANO SCARSELLI; Phone Number: +39 3382985555; Email: cristiano.scarselli@gmail.com

Study Locations

• Italy
  • Arezzo
    • Montevarchi, Arezzo, Italy, 52025
      • Recruiting
      • CLINICA DI RIABILITAZIONE TOSCANA Spa
      • Contact: CRISTIANO SCARSELLI; Phone Number: +39 3382985555; Email: cristiano.scarselli@gmail.com
      • Contact: LAURA ABBRUZZESE; Phone Number: +39 3473333750; Email: laura.abbruzzese@libero.it

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 20 years to 80 years (Adult, Older Adult)
• Accepts Healthy Volunteers: No

Description

Inclusion Criteria:

• Subjects of both gender, with ischaemic stroke;
• Left hemispheric injury documented by neuroimaging examination;
• Cerebrovascular disease onset within the first 30 days;
• Presence of ideomotor apraxia as documented by a score < 53 in the De Renzi's test;
• Intact semantic skills as documented by normal performance on the Auditory or Visual Word Comprehension subtest of the Neuropsychological Examination for Aphasia (E. N. P. A.);
• Full comprehension skills as documented by normal performance in the sub-test of oral or orthographic comprehension (Auditory or Visual Words Comprehension) of the Neuropsychological Examination for Aphasia (E. N. P. A.);
• Age between 20 and 80 years;
• Any schooling;
• Patient's informed consent signature.

Exclusion Criteria:

• Comprehension and/or semantics deficit as documented by E. N. P. A.;
• Pre-existing psychiatric and/or neurological pathology;
• Failure to sign the patient's and/or caregiver's informed consent.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Supportive Care
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: Double

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: transcranial Direct Current Stimulation (tDCS); transcranial Direct Current Stimulation (tDCS) on the left posterior parietal cortex and rehabilitative treatment with Smania's training	Device: transcranial Direct Current Stimulation (tDCS); Direct current transcranial stimulation will be applied for 20 minutes over the left posterior parietal cortex with an intensity set to 2 mA.; Device: Behavioural; Treatment for upper limbs ideomotor apraxia (Smania et al., 2000)
Sham Comparator: Placebo stimulation (sham-tDCS); Placebo stimulation and rehabilitative treatment with Smania's training	Device: Behavioural; Treatment for upper limbs ideomotor apraxia (Smania et al., 2000); Device: Sham stimulation (sham-tDCS); The same positioning of electrodes as the stimulation condition will be used, but the current will be applied for 30 seconds and then progressively reduced.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Changes from baseline Ideomotor apraxia test	It consists of 24 imitation tests carried out with the fingers, the hand and the limb homolateral to the lesion. Each gesture is presented up to three times if the production is incorrect, and receives a score of 3 to 0 depending on whether the copy is correct the first, the second, the third time, or never. The test includes 24 gestures, 12 symbolic and 12 non-symbolic, for a total score of 72. Application of the test to over 200 normal subjects showed that the diagnosis of apraxia can be made reliably when the score drops below 53, it's probable, but not certain, for a score between 53 and 62, and it's excluded when the score is greater than 62.	The first day of treatment; End of 2nd week; End of 3rd week
Changes from baseline Standardized test for the diagnosis of a selective ideomotor apraxia deficit on the basis of gesture and effector types	Test for ideomotor apraxia assessment which allows to highlight: 1) the selective deficits for the type of gesture to be imitated and, therefore, specific damage to the two processes underlying the imitation (direct route and semantic pathways) presenting known and new gestures in separate blocks; and 2) deficits of the distal or proximal component of the movements.	The first day of treatment; End of 2nd week; End of 3rd week
Changes from baseline Ideational apraxia test	By placing in front of the patient one object at a time, he is asked to perform the pantomime of use of the object without touching or holding the object itself, but only by looking at it (visual mode). The examiner will assign 2 points if the execution is correct, 1 point if the execution is correct after repetition of the command and 0 points for always incorrect execution. The objects used are: glass, screwdriver, comb, gun, fork, key, rubber, saw, hammer, fan.	The first day of treatment; End of 2nd week; End of 3rd week

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Changes from baseline Oral apraxia test	The examiner mimics the 10 bucco-facial movements required by the protocol, and asks the patient to imitate them. If the subject does not perform the task or does not perform it correctly, the therapist repeats the gesture a second time. If, again, the patient does not perform or makes a mistake, the next stimulus is taken. Maximum time for each stimulus is 30 seconds. The gestures to imitate are: show your tongue, whistle, yawn, try to lick your nose, make a partridge, give a kiss, show how your teeth shake when it's cold, snap your tongue making the sound of a galloping horse, blow and scratch your throat. The score is 2 if the execution is accurate on the first attempt, 1 if it is correct on the second attempt and 0 if the gesture is not executed or is not reproduced correctly.	The first day of treatment; End of 2nd week; End of 3rd week
Changes from baseline Jebsen-Taylor Hand Functional Assessment Scale	It is a scale that allows to assess the level of hand function during daily activities. It consists of 7 subtests: writing, turning a page, lifting small objects, pantomime of eating, stacking objects, lifting large and light objects and large and heavy objects. The non-dominant hand will be tested first and then the dominant one. The time for each item will be timed: the final score (total time) will be given by the sum of all the part times: the lower the score, the better the level of hand function.	The first day of treatment; End of 2nd week; End of 3rd week

Collaborators and Investigators

• Sponsor: Clinica di Riabilitazione Toscana Spa
• Collaborators: FONDAZIONE GIANFRANCO SALVINI ONLUS
• Investigators: Principal Investigator: CRISTIANO SCARSELLI, CLINICA DI RIABILITAZIONE TOSCANA Spa

Study record dates

Study Major Dates

• Study Start (Actual): February 2, 2022
• Primary Completion (Estimated): March 1, 2024
• Study Completion (Estimated): March 1, 2024

Study Registration Dates

• First Submitted: February 15, 2022
• First Submitted That Met QC Criteria: February 17, 2022
• First Posted (Actual): February 28, 2022

Study Record Updates

• Last Update Posted (Actual): September 7, 2023
• Last Update Submitted That Met QC Criteria: September 6, 2023
• Last Verified: September 1, 2023

More Information

Terms related to this study

• Keywords: transcranial direct current stimulation; stroke rehabilitation
• Additional Relevant MeSH Terms: Nervous System Diseases; Neurologic Manifestations; Neurobehavioral Manifestations; Psychomotor Disorders; Apraxias; Apraxia, Ideomotor
• Other Study ID Numbers: tDCS-AIM

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No