Stroke, Cognitive Impairment
Conditions
Keywords
transcranial direct current stimulation (tDCs), neurofeedback
Brief summary
This is a double blinded, randomized control trial with a pretest-posttest control and interventional groups design. Both the assessor and participants are blinded to all assessments and evaluations. All patients with subacute stroke undergo in-patient or out-patient rehabilitation are screened initially by a series of screening test. Suitable patients are assigned randomly to 3 groups respectively. Group 1 is the combined transcranial direct current stimulation (tDCS) and neurofeedback group. Group 2 is the neurofeedback group. Group 3 is the control group with sham neurofeedback training.
Detailed description
Treatment sessions for all three groups are conducted by the investigators who has training in neurofeedback and transcranial direct current stimulation (tDCs). Each participant performed 10 training sessions on different days. Sessions were conducted 3-5 times a week The tDCS + neurofeedback group will carry out 30 minutes tDCS and 30 minutes neurofeedback training. The real neurofeedback group will carry out 30 minutes neurofeedback training. The sham neurofeedback group will conduct the 30 minutes sham neurofeedback training.
Interventions
DEVICEtDCS & neurofeedback
tDCs and neurofeedback
DEVICEneurofeedback
Neurofeedback
DEVICEsham neurofeedback
sham neurofeedback
Sponsors
Chinese University of Hong Kong
Kowloon Hospital, Hong Kong
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Healthy volunteers
No
Inclusion criteria
1. First or second stroke (haemorrhagic or ischaemic) confirmed by computer axial tomography scan or magnetic resonance imaging 2. Below 16 th percentile cut off in Hong Kong Montreal - Cognitive Assessment (HK - MoCA) (range from 17-25/30). 3. Less than twelve months since onset of stroke at study entry 4. Able to follow simple command
Exclusion criteria
1. Patients with severe dysphasia (either expressive or comprehensive) which restricts communication; 2. History of other neurological disease, psychiatric disorder, or alcoholism; 3. Significant impairment in visual or auditory function 4. Any additional medical or psychological condition that would affect their ability to comply with the study protocol.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Change score in Trail Making Test A & B from baseline | One day before the treatment , up to 4 weeks, up to 16 weeks | Trail Making Test is a neuropsychological test of visual attention and task switching. It consists of two parts in which the subject is instructed to connect a set of 25 dots as quickly as possible while still maintaining accuracy. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Change score in Functional Independence Measure (FIM) from baseline | One day before the treatment , up to 4 weeks, up to 16 weeks | The Functional Independence Measure instrument is a basic indicator of patient disability. FIM is used to track the changes in the functional ability of a patient during an episode of hospital rehabilitation care. |
| Change score in Stroke Adapted 30 item version of the Sickness Impact Profile (SA - SIP 30) | One day before the treatment , up to 4 weeks, up to 16 weeks | SA-SIP 30 assesses quality of life in patients who have sustained a stroke. |
Countries
Hong Kong
Outcome results
None listed