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NonInvasive Brain Stimulation in Stroke Patients

A Randomised Trial of Non-Invasive Brain Stimulation (NIBS) in Stroke Survivors

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02401724
Acronym
RTNIBS
Enrollment
60
Registered
2015-03-30
Start date
2015-03-31
Completion date
2018-06-30
Last updated
2015-03-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stroke

Keywords

Hemispatial neglect, Transcranial direct current stimulation, Rehabilitation

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.

Interventions

OTHERTranscranial direct current stimulation
OTHERAction Training

Sponsors

University of Glasgow
CollaboratorOTHER
NHS Greater Glasgow and Clyde
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
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

Design outcomes

Primary

MeasureTime frame
Change in Behavioural Inattention Test (BIT)6 months post intervention

Secondary

MeasureTime frame
Compliance as measured by adherence to task instructions (percentage of intervention sessions, BIT tests completed)baseline
Retention Numbersbaseline

Contacts

Primary ContactMonika Harvey, BSc (hons), MSc, PhD
monika.harvey@glasgow.ac.uk01413306174

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 18, 2026