RTNIBS: NonInvasive Brain Stimulation in Stroke Patients

Sponsor
NHS Greater Glasgow and Clyde (Other)
Overall Status
Unknown status
CT.gov ID
NCT02401724
Collaborator
University of Glasgow (Other)
60
4
39

Study Details

Study Description

Brief Summary

After a stroke affecting the right side of the brain, many patients are affected by "spatial neglect": the damage to the brain causes them to ignore the left side of their surroundings. At its most extreme they may be unaware that they have a left side, or believe that it is moving normally when it is in fact paralysed. In milder cases, people may be unable to recognise touch on the left side if their right side is also being touched, or objects in their left visual field if something is visible to their right. Neglect alters peoples' quality of life profoundly, often renders them more dependent on others to undertake basic activities of daily living, and makes effective rehabilitation much more difficult.

The limited success of current treatment approaches indicates gaps in understanding of the underlying mechanisms of neglect and its recovery. Recent data suggest that the problems in responding to the left side are a result of an imbalance of activity in those parts of the brain responsible for deciding which side to pay attention to. It might therefore be possible to help people with neglect by "rebalancing" the brain either by increasing activity in the damaged side, or alternatively by reducing activity in the undamaged side. In this pilot study, the investigators will test whether they can help by doing the second of these things.

The investigators propose to conduct a pilot clinical trial to explore whether using electric currents to temporarily modify the activity of specific areas of the intact side of the brain, influences recovery from neglect, when used either alone, or in combination with a training method that has previously appeared promising as a treatment. Brain activity will be modified using a technique called "transcranial direct current stimulation (tDCS)", in which small electric currents are applied to the scalp with a wire covered in damp cotton pads. This will be done over the specific parts of the brain that are responsible for focusing attention to one side.

The investigators will compare the clinical outcomes of four interventions (1: behavioural, 2: tDCS, 3: a combination of both and 4: control).

The investigators hope that these studies will advance their understanding of what treatments may help people with neglect, and how they might work.

Condition or Disease Intervention/Treatment Phase
  • Other: Transcranial direct current stimulation
  • Other: Action Training
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
60 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
A Randomised Trial of Non-Invasive Brain Stimulation (NIBS) in Stroke Survivors
Study Start Date :
Mar 1, 2015
Anticipated Primary Completion Date :
Jun 1, 2018
Anticipated Study Completion Date :
Jun 1, 2018

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Action Training

Training exercise which involves patients lifting up rods of different sizes and shifting their grip if this is too far to one side

Other: Action Training

Experimental: tDCS

A constant 1mA current will be applied to the left (undamaged) side of the scalp with an electrode covered with a damp cotton pad (25 cm2). The current will be applied for 15 minutes per day, with a total of 10 sessions over 3 weeks.

Other: Transcranial direct current stimulation
Other Names:
  • tDCS
  • Experimental: Action Training + tDCs

    This will involve the same procedure as in action training only but with tDCS applied for 15 minutes during the rodlifting.

    Other: Transcranial direct current stimulation
    Other Names:
  • tDCS
  • Other: Action Training

    Placebo Comparator: Control training

    For the control training, patients will be asked to simply reach for the right hand side of each rod with their right (unaffected) hand and lift it

    Outcome Measures

    Primary Outcome Measures

    1. Change in Behavioural Inattention Test (BIT) [6 months post intervention]

    Secondary Outcome Measures

    1. Compliance as measured by adherence to task instructions (percentage of intervention sessions, BIT tests completed) [baseline]

    2. Compliance as measured by adherence to task instructions (percentage of intervention sessions, BIT tests completed) [3 weeks]

    3. Compliance as measured by adherence to task instructions (percentage of intervention sessions, BIT tests completed) [6 months]

    4. Retention Numbers [baseline]

    5. Retention Numbers [3 weeks]

    6. Retention Numbers [6 months]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 90 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    1. Ischemic stroke affecting the right hemisphere, confirmed by CT or MRI.

    2. Persistent neglect for one month after ictus (confirmed by BIT).

    3. Prestroke functional independence (modified Rankin Scale score 0-2).

    4. Between 18-90 years of age

    Exclusion Criteria:
    1. Patients younger than 18.

    2. Patients who do not understand verbal or written English (ie.need of translaters)

    3. bilateral infarcts (Confirmed by CT, MRI)

    4. Dementia (MOCA, Score <26).

    5. Neurological Disease (eg. Parkinson's Disease, epilepsy, MS)

    6. Significant morbidity (eg cancer, severe cardiac failure) likely to affect participation.

    7. Alcohol excess (more than 50/40 units a week for men/women respectively).

    8. Patients who fall under the exclusion criteria for TDCS which includes patients suffering from a stroke related seizure :

    History of epilepsy, medications or psychoactive drugs that can lower seizure threshold [imipramine, amitriptyline, doxepine, nortriptyline, maprotiline, chlorpromazine, clozapine, foscarnet, ganciclovir, ritonavir, amphetamines, cocaine, (MDMA, ecstasy), phencyclidine (PCP, angel dust), ketamine, gammahydroxybutyrate (GHB), alcohol, theophylline]. Withdrawal from alcohol, barbiturates, benzodiazepines, meprobamate, chloral hydrate. Patients who are pregnant or have suffered from a stroke-related seizure.

    Contacts and Locations

    Locations

    No locations specified.

    Sponsors and Collaborators

    • NHS Greater Glasgow and Clyde
    • University of Glasgow

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    NHS Greater Glasgow and Clyde
    ClinicalTrials.gov Identifier:
    NCT02401724
    Other Study ID Numbers:
    • GN13NE562
    First Posted:
    Mar 30, 2015
    Last Update Posted:
    Mar 30, 2015
    Last Verified:
    Mar 1, 2015
    Keywords provided by NHS Greater Glasgow and Clyde
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Mar 30, 2015