Stroke. I64 Stroke, not specified as haemorrhage or infarction
Conditions
Interventions
Intervention 1: Intervention group: Intervention group will receive visual scanning exercises along with task-specific approach. Intervention 2: Control group: Control group will receive task-specific
Sponsors
University of Lahore, main campus
Eligibility
Sex/Gender
All
Age
19 Years to 60 Years
Inclusion criteria
Inclusion criteria: Patients who suffered with eye-movement disorder either an ischemic or hemorrhagic stroke Clinically diagnosed by a neurologist Information on the type of stroke will be obtained from the patients’ medical records Both male and female patients between the age group of 19–60 years Minimum score of 7 on Mini-Mental State Examination (MMSE) Patients in the sub-acute stage after the stroke and able to follow instructions and have the capacity to provide informed consent
Exclusion criteria
Exclusion criteria: Repeated stroke Severe dementia, identified by applying the MMSE History of an organic disorder or major psychiatric impairment Disability or other comorbid disease such as cancer or amputation that will limit or prevent assessment of the patients Participation in other interventional or pharmacological studies which can affect the results of this study Patients with vestibular problems who have positive dix-hallpike test Patients with facial palsy • Patients with ophthalmological problems before stroke onset Patients suffering from balance problems as a result of muscular problem
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Berg balance scale. Timepoint: Before intervention and at 4 weeks of intervention. Method of measurement: Scoring. | — |
Secondary
| Measure | Time frame |
|---|---|
| Dynamic gait index scale to assess the gait impairments and risk of fall. Timepoint: Before and after 4 weeks of intervention. Method of measurement: A four -point ordinal scale ranging from 0-3 will be used.;Barthel index scale to measure the activities of daily living functions. Timepoint: Before and after 4 weeks of intervention. Method of measurement: A three -point ordinal scale ranging from 0-2 will be used. | — |
Countries
Pakistan
Contacts
Public ContactDr. Sana Batool, PT
University of Lahore
Outcome results
None listed