Combining tDCS With VR-based Motor Training in Stroke

NCT03144102 | Unknown

• 1 other identifier: tDCSRGS
• Study Type: interventional
• Target: 36
• Locations: 1 country
• Sites: 1

Brief Summary

Stroke represents one of the main causes of adult disability and will be one of the main contributors to the burden of disease in 2030. However, our healthcare systems do not have enough resources to cover the current demand let alone its future increase. There is a need to deploy new approaches that advance the current rehabilitation methods and enhance their efficiency. One of the latest approaches used for the rehabilitation of a wide range of deficits of the nervous system is based on virtual reality (VR) applications, which combine training scenarios with dedicated interface devices. On the other hand, recent studies have shown the potential of transcranial direct current stimulation (tDCS) to restore motor function in hemiparetic stroke patients. It must be emphasized, however, that so far little work exists on the quantitative assessment of the clinical impact of VR based approaches in combination with tDCS protocols. We hypothesize that the combination of VR-based motor rehabilitation protocols with concurrent anodal tDCS can boost functional recovery, and may achieve superior effects when compared to 3 alternative treatments: 1) VR without tDCS, 2) occupational therapy with tDCS, and 3) occupational therapy without tDCS. The findings derived from this study will contribute to establish a novel and superior neurorehabilitation paradigm that can accelerates the recovery of hemiparetic stroke patients. Besides the clinical impact, such achievement could have relevant socioeconomic impact.

Conditions

Virtual Reality Based Therapy; Anodal tDCS; Occupational Therapy; Sham tDCS

Outcome Measures

Primary Outcomes (1)

• Change of arm/hand function as captured by the upper extremity Fugl-Meyer assessment scale

  At baseline, at 2-weeks (after intervention), and at 8-weeks (follow-up)

Secondary Outcomes (5)

• Change of Independence as captured by Barthel scale

  At baseline, at 2-weeks (after intervention), and at 8-weeks (follow-up)

• Change of motor function in ADLs as captured by Chedoke Arm and Hand Activity Inventory (CAHAI) scale

  At baseline, at 2-weeks (after intervention), and at 8-weeks (follow-up)

• Change of interhemispheric balance as captured by EEG recordings

  At baseline, at 2-weeks (after intervention), and at 8-weeks (follow-up)

• Change of spasticity in proximal and distal muscles as captured by Ashworth scale

  At baseline, at 2-weeks (after intervention), and at 8-weeks (follow-up)

• Change of spatial hemineglect as captured by the Star cancellation test

  At baseline, at 2-weeks (after intervention), and at 8-weeks (follow-up)

Study Arms (4)

VR-based motor rehabilitation with tDCS

EXPERIMENTAL

Behavioral: Virtual Reality-based therapy for upper-limbs motor rehabilitation; Device: Anodal transcranial direct-current stimulation (tDCS)

Occupational Therapy with tDCS

ACTIVE COMPARATOR

Device: Anodal transcranial direct-current stimulation (tDCS); Behavioral: Occupational Therapy for upper-limbs motor rehabilitation

VR-based motor rehabilitation with sham tDCS

SHAM COMPARATOR

Behavioral: Virtual Reality-based therapy for upper-limbs motor rehabilitation; Device: Sham transcranial direct-current stimulation (tDCS)

Occupational Therapy with sham tDCS

SHAM COMPARATOR

Behavioral: Occupational Therapy for upper-limbs motor rehabilitation; Device: Sham transcranial direct-current stimulation (tDCS)

Interventions

Virtual Reality-based therapy for upper-limbs motor rehabilitation BEHAVIORAL

During each session, the subject will perform 4 VR-based exercises that involve reaching, grasping, and intercepting virtual objects. The training will last a total of 30 min per session.

VR-based motor rehabilitation with sham tDCS; VR-based motor rehabilitation with tDCS

Anodal transcranial direct-current stimulation (tDCS) DEVICE

Concurrent anodal tDCS on sensorimotor cortex on the ipsilesional hemisphere.

Occupational Therapy with tDCS; VR-based motor rehabilitation with tDCS

Occupational Therapy for upper-limbs motor rehabilitation BEHAVIORAL

During each session, the subject will perform 4 occupational therapy exercises that involve reaching, grasping, and intercepting objects. The training will last a total of 30 min per session.

Occupational Therapy with sham tDCS; Occupational Therapy with tDCS

Sham transcranial direct-current stimulation (tDCS) DEVICE

Concurrent sham tDCS on sensorimotor cortex on the ipsilesional hemisphere.

Occupational Therapy with sham tDCS; VR-based motor rehabilitation with sham tDCS

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Patients with hemiparesis secondary to first ever ischemic or hemorrhagic stroke (Medical Research Council score \> 2).
• Older than 18 years old.
• Sufficient cognitive capacity to understand and follow the experimental instructions (Mini-Mental State Evaluation \> 20).

You may not qualify if:

• Presence of a condition or abnormality that in the opinion of the Investigator would compromise the safety of the patient or the quality of the data.
• Epilepsia and metal implants. A diagnostic EEG will be performed by the Department of Clinical Neurophysiology of the hospital to detect epileptic paroxysmal in order to include or exclude patients in the study.
• Low Cognitive capabilities that prohibits the execution of the experiment Arteriovenous malformation
• Severe associated impairment such as spasticity, communication disabilities (sensorial, mixed or global aphasia or apraxia), major pain or other neuromuscular impairments or orthopaedic devices that would interfere with the correct execution of the experiment (Modified Ashworth Scale \> 3)
• History of serious mental-health problems in acute or sub acute phase
• Refusal to sign the consent form
• Previous surgeries opening the skull.
• Active or recent substance abuse or dependence within the past year.
• Pregnancy, breastfeeding, unwillingness to practice birth control during participation in the study.

Sponsors & Collaborators

• Universitat Pompeu Fabra: lead
• Neuroelectrics Corporation: collaborator

Study Sites (1)

Unitat de Rehabilitació de l'Hospital Vall d'Hebron

Barcelona, 08035, Spain

RECRUITING

MeSH Terms

Interventions

Transcranial Direct Current Stimulation; Occupational Therapy

Intervention Hierarchy (Ancestors)

Electric Stimulation Therapy; Therapeutics; Convulsive Therapy; Psychiatric Somatic Therapies; Behavioral Disciplines and Activities; Electroshock; Psychological Techniques; Rehabilitation; Aftercare; Continuity of Patient Care; Patient Care

Central Study Contacts

Paul Verschure, Prof.

CONTACT

0034935422202; paul.verschure@upf.edu

Belén Rubio, PhD

CONTACT

0034935422202; belen.rubio@upf.edu

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: QUADRUPLE
• Who Masked: PARTICIPANT, CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
• Purpose: TREATMENT
• Intervention Model: FACTORIAL
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Prof.

Study Record Dates

• First Submitted: May 4, 2017
• First Posted: May 8, 2017
• Study Start: May 15, 2017
• Primary Completion: December 8, 2020
• Study Completion: June 8, 2021
• Last Updated: August 10, 2020

Record last verified: 2020-08

Locations

ES (1)