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Completed

NCT Number: NCT02725853

Enhancing Recovery of Arm Movement in Stroke Patients

Many people who have had a stroke have problems recovering the use of their affected arm and these problems may persist for a long time. The investigators' research will test new ways to boost recovery by using non-painful brain stimulation together with training of arm movements using basic science principles. The training program will be done using the latest technology in rehabilitation such as virtual reality and robotics. The investigators will compare three groups of patients who have had a stroke. Each group will receive different combinations of brain stimulation and arm training. Another aspect of this proposal is that the investigators will do the same training programs in three different countries - Canada, Israel and India. In this way, the investigators will combine knowledge and skills to create training programs that can be applied anywhere in the world and that are not necessarily limited to high-income countries. Also, by combining expertise, the investigators will help to build the capacity to do research in India, a middle-income country that has great potential to contribute new knowledge to rehabilitation medicine.

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Key information

Age range

25 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

CRIR

Montreal, Quebec, H2H2N8, Canada

About this study

Training approaches based on established principles of motor learning and neural plasticity and non-invasive brain stimulation such as repetitive Transcranial Magnetic Stimulation and transcranial Direct Current Stimulation (tDCS) show promise in modulating brain activity in order to enhance upper limb (UL) motor recovery. However, the potential for recovery may still not be attained if training programs do not specifically focus on remediating motor impairment as defined by motor control science. This project is driven by a major theory of motor control (Threshold Control Theory) suggesting that rather than directly specifying motor commands to muscles, descending systems regulate spatial thresholds (STs) of reflexes to generate and control voluntary movement within specific areas of joint space. In patients with stroke, ST control is diminished leading to the appearance of muscle spasticity, weakness and abnormal muscle activation patterns during voluntary movement within well-defined spatial (angular) zones. The investigators hypothesize that recovery of voluntary motor control is tightly linked to the recovery of threshold control. The investigators propose a training program that incorporates personalized tDCS to balance cortical hypo/hyperexcitability as well as personalized movement arm reaching training based on the identification of disorders in ST.

Overall objectives of the proposal are:

  • To test the effectiveness of personalized training programs to increase the range of regulation of STs in the elbow during reaching.
  • To determine the effects of repetitive tDCS aimed at inhibiting excessive/exciting diminished cortical activity.
  • To determine the feasibility of implementing personalized training programs in high and low-to-middle income countries.

Sixty patients with sub-acute (3 wks-6 mos) stroke will be recruited in this multi-site international trial taking place in Canada, Israel and India. Participants will have spasticity in the elbow flexors and/or extensors, with some active elbow control. Each site will recruit and randomize patients into one of 3 treatment groups. Group 1 will receive tDCS and practice personalized arm motor training. Group 2 will also receive tDCS with non-specific practice. Group 3 will receive Sham-tDCS and personalized practice. Training will consist of the application of tDCS in the first 30 minutes of a 50-minute arm reaching practice session,, 5 days per week for 2 weeks. Primary outcome measures (Pre, Post, Follow-up) are elbow flexor and extensor STs and related spasticity/active control zones. Secondary measures are clinical measures of UL motor activity. By accounting for the spatial structure of motor deficits, our research will benefit both researchers and clinicians by advancing our understanding of the mechanisms underlying unimpaired/impaired motor control and recovery.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • first ever cortical or cortical/subcortical stroke confirmed by MRI/CT and medically stable;
  • sub-acute stage of stroke (3 wk to 6 mo post-stroke);
  • arm paresis (Chedoke-McMaster Arm Scale of 2-6 /7; Gowland et al. 1993) but able to perform voluntary elbow flexion/extension of at least 30° per direction;
  • elbow flexor and/or extensor spasticity (> 1+/4 on Modified Ashworth Scale; Ashworth 1964; Bohannon and Smith 1987);
  • able to provide informed consent.

Exclusion criteria

  • major neurological (other than stroke) / neuromuscular / orthopaedic problems or pain that may interfere with interpretation of results;
  • major cognitive deficits (a score <20 on the Montreal Cognitive Assessment, Nasreddine et al. 2005);
  • history of psychiatric disorders, alcohol or drug abuse, skin sensitivity, seizures, migraines, metal in cranium and other implants (cochlear, cardiac);
  • taking medications (e.g. epileptic and psychoactive drugs) that could affect brain activity (Poreisz 2007).

Treatment and study plan

tDCS

Device

Application of 1.5 mA tDCS for 30 minutes

Sham tDCS

Device

Application of sham tDCS for 30 minutes

personalized practice

Behavioral

arm exercise consisting of whole arm movement within a restricted elbow range of motion

non-personalized practice

Behavioral

arm exercise consisting of unrestricted whole arm movement

Primary outcomes

  1. Change in active control zone of the elbow

    Time frame: 2 weeks and 1 month

    Post-test and Follow-up test; measured using motion analysis system.

Secondary outcomes

  1. Change in Fugl-Meyer Assessment of arm impairment score

    Time frame: 2 weeks and 1 month

    Post-test and Follow-up test; Score of 66 points indicates normal functioning.

  2. Change in spasticity score

    Time frame: 2 weeks and 1 month

    Post-test and Follow-up test; 6 point ordinal scale

  3. Change in streamlined Wolf Motor Function Test score

    Time frame: 2 weeks and 1 month

    Post-test and Follow-up test;30 point ordinal scale

  4. Change in active range of elbow extension

    Time frame: 2 weeks and 1 month

    Post-test and Follow-up test; measured with a hand-held goniometer

  5. Change in straightness of elbow trajectory during a reach to grasp task

    Time frame: 2 weeks and 1 month

    Post-test and Follow-up test; measured using a motion analysis system

  6. Change in speed of endpoint movement during a reach to grasp task

    Time frame: 2 weeks and 1 month

    Post-test and Follow-up test; measured using a motion analysis system

  7. Change in smoothness of endpoint trajectory during a reach to grasp task

    Time frame: 2 weeks and 1 month

    Post-test and Follow-up test; measured using a motion analysis system

Sponsors and collaborators

Lead sponsor

McGill University

Other

Collaborators

  • Manipal University
  • Tel Aviv University

Registry information

Official study title

ENHANCE: Enhancing Brain Plasticity for Sensorimotor Recovery in Spastic Hemiparesis

Acronym: ENHANCE

Important dates

Study start
2016
Primary completion
2020
Study completion
2021
First posted
Apr 1, 2016
Registry last updated
Jan 3, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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