Skip to content

Electroencephalogram-neurofeedback (EEG-NF) to improve neglect in stroke patients

A novel neurofeedback-based intervention to reduce neglect and improve function in stroke patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN85291842
Enrollment
72
Registered
2008-12-10
Start date
2009-02-01
Completion date
Unknown
Last updated
2017-05-08

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

Conditions

Stroke rehabilitation Circulatory System Stroke, not specified as haemorrhage or infarction

Interventions

In the intervention group, patients will receive a 30-minute session of EEG-NF training, 5 days a week for a total duration of 6 weeks (30 sessions). The EEG will be recorded from three sensors placed

Sponsors

East Kent Hospitals University NHS Trust (UK)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Two to 12 weeks from stroke onset 2. First ever stroke 3. Right hemisphere cortical involvement, confirmed on neuroimaging 4. Significant visual neglect, defined as a behavioural inattention test (BIT) score of 129 or less (maximum possible 146) 5. No other significant cognitive or communication problem 6. Informed consent for participation and follow-up 7. Both sexes, aged 18 - 85 years

Exclusion criteria

Exclusion criteria: 1. Unable to provide consent 2. Unable to comply with training or assessment procedures for any reason

Design outcomes

Primary

MeasureTime frame
The Behavioural Inattention Test (BIT) measured at 6 weeks after randomisation. BIT will also be measured 12 weeks after randomisation (6 weeks after completion of EEG-NF training) to assess sustainability.

Secondary

MeasureTime frame
1. Attentional Network Test (ANT), measured 6 and 12 weeks after randomisation 2. Barthel Index (BI), measured 6 and 12 weeks after randomisation 3. Nottingham Extended Activities of Daily living (NEADL) for activity and participation, measured 6 and 12 weeks after randomisation 4. Hospital Anxiety and Depression Scale (HADS) for mood, measured 6 and 12 weeks after randomisation 5. Five dimensional EuroQol (EQ-5D) and the visual analogue scale (EQ-VAS) for quality of life, measured 6 and 12 weeks after randomisation 6. Quantitative-EEG (Q-EEG) and functional magnetic resonance imaging, measured at baseline and 6 weeks in 36 patients to investigate underlying cortical changes with recovery and intervention 7. The number of patients consenting to EEG-NF training, number completing the programme, sessions completed and ability to modulate various EEG frequencies will be documented to assess acceptability 8. Ease of use including staff training requirements and the feasibility of integrating with existing therapy programmes 9. The semi-structured interview will be analysed for patient views on benefits of treatment, acceptability of training and perceived benefits of the training programme

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026