NonInvasive Brain Stimulation in Stroke Patients

Stroke Clinical Trial

— RTNIBS  

Official title:

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

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT02401724
• Other study ID #: GN13NE562
• Status: Not yet recruiting
• Phase: N/A
• First received: March 10, 2015
• Last updated: March 27, 2015
• Start date: March 2015
• Est. completion date: June 2018

Study information

• Verified date: March 2015
• Source: NHS Greater Glasgow and Clyde
• Contact: Monika Harvey, BSc (hons), MSc, PhD
• Phone: 01413306174
• Email: monika.harvey[@]glasgow.ac.uk
• Is FDA regulated: No
• Health authority: United Kingdom: National Health Service
• Study type: Interventional

Clinical Trial 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.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 60
• Est. completion date: June 2018
• Est. primary completion date: June 2018
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years to 90 Years

Eligibility

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.

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Stroke

Intervention

Other:
• Transcranial direct current stimulation

• Action Training

Locations

Country	Name	City	State
n/a

Sponsors (2)

Lead Sponsor	Collaborator
NHS Greater Glasgow and Clyde	University of Glasgow

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change in Behavioural Inattention Test (BIT)		6 months post intervention	No
Secondary	Compliance as measured by adherence to task instructions (percentage of intervention sessions, BIT tests completed)		baseline	No
Secondary	Compliance as measured by adherence to task instructions (percentage of intervention sessions, BIT tests completed)		3 weeks	No
Secondary	Compliance as measured by adherence to task instructions (percentage of intervention sessions, BIT tests completed)		6 months	No
Secondary	Retention Numbers		baseline	No
Secondary	Retention Numbers		3 weeks	No
Secondary	Retention Numbers		6 months	No