Skip to content

Hemianopia Activity-Based InTervention (HABIT): refining and operationalising a rehabilitation intervention for visual field loss after stroke

Hemianopia Activity-Based InTervention (HABIT): refining and operationalising a rehabilitation intervention for visual field loss after stroke

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN54718796
Enrollment
34
Registered
2020-10-06
Start date
2020-10-12
Completion date
Unknown
Last updated
2021-02-08

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

Conditions

Stroke Circulatory System Stroke, not specified as haemorrhage or infarction

Interventions

Occupational therapy visual rehabilitation intervention (hemianopia activity-based intervention). The main outcome from this study is the HABIT intervention itself which will comprise

Sponsors

North Bristol NHS Trust
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. New stroke being managed on a stroke rehabilitation pathway 2. Presence of visual field defect on screening such as confrontation visual field testing e.g. as part of the NIHSS 3. Confirmation of visual field defect using perimetry 4. Visual field defect considered by a HABIT study trained OT to be causing difficulty with meaningful goals for rehabilitation 5. Willing and have capacity to provide informed consent to participate in the study

Exclusion criteria

Exclusion criteria: 1. Visual neglect severe enough to prevent any orientation beyond the midline to the affected side assessed by a treating clinician 2. Living outside of an area covered by the early supported discharge services or community providers associated with the recruiting centre if they are being discharged from inpatient services with ongoing therapy

Design outcomes

Primary

MeasureTime frame
The main outcome from this study is the HABIT intervention itself which will comprise an online training, education and intervention tool with accompanying manual and description for replicating the intervention in future clinical studies.

Secondary

MeasureTime frame
Secondary outcomes relating to future implementation and delivery in a clinical trial are detailed below: 1. Measuring recruitment and retention rates for a future clinical trial 2. Evaluating the feasibility of using the Canadian Occupational Performance Measure (COPM) as an outcome measure in a future evaluation 3. Evaluating the range of clients with whom HABIT can usefully be employed 4. Acceptability for patients, carers, therapists, therapy assistants and support workers

Countries

United Kingdom

Outcome results

None listed

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