Skip to content

Functional Effects of Prism Adaptation Training in Stroke Patients with Spatial Neglect

Functional Effects of Prism Adaptation Training in Stroke Patients with Spatial Neglect

Status
Terminated
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12605000539639
Enrollment
100
Registered
2005-09-28
Start date
2005-02-09
Completion date
Unknown
Last updated
2020-01-13

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

Conditions

None listed

Brief summary

This study will clarify the effectiveness of prism adaptation treatment for stroke patients with hemi-spatial neglect. The treatment group will undergo five training sessions while wearing prism glasses. The control group will undergo the same procedure while wearing sham glasses. The two groups will be compared for improvements in the neglect impairment and in functional abilities.

Interventions

Patients are randomly assigned to experimental / control groups. Experimental subjects undergo prism adaptation (PA) training for five sessions over two weeks in addition to usual care. (PA training consists of 30 reaches for targets while wearing 15 degree right deviating prism glasses.) Double blinded FIM and Catherine Bergego Scale scores are assessed on hospital admission and discharge. Additional tests include: letter cancellation, figure copying, TUGT walking test, seated reach test, and

Patients are randomly assigned to experimental / control groups. Experimental subjects undergo prism adaptation (PA) training for five sessions over two weeks in addition to usual care. (PA training consists of 30 reaches for targets while wearing 15 degree right deviating prism glasses.) Double blinded FIM and Catherine Bergego Scale scores are assessed on hospital admission and discharge. Additional tests include: letter cancellation, figure copying, TUGT walking test, seated reach test, and Fluff test. Mailed survey follow up at 4 months includes Stroke Impact Scale (SIS-16) and depression screening (CESD-10).

Sponsors

orthern Rivers University Department of Rural Health
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Blinded (masking used)

Eligibility

Sex/Gender
All
Age
55 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Stroke occurring within the previous 60 days with clinical evidence of neglect (Bergego >1); Able perform test procedures (patients with hemianopia WILL be included); Medically stable.

Exclusion criteria

Brainstem stroke or subarachnoid hemorrhage; Secondary neurological illness (e.g. Parkinsons, MS); Dementia (MMSE>23).

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026