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Visual and Tactile Scanning Training in Patients With Neglect After Stroke

Visual and Tactile Scanning Training in Patients With Neglect After Stroke

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02309853
Acronym
ViTaTrain
Enrollment
16
Registered
2014-12-05
Start date
2014-12-31
Completion date
2015-12-31
Last updated
2014-12-05

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

Conditions

Hemispatial Neglect

Brief summary

The purpose of this study is to evaluate whether 20 Sessions of 30 minutes with a visual and tactile scanning training in the personal, peripersonal and extrapersonal space combined with trunk rotation will be feasible and provide better results compared to 20 Sessions of 30 minutes of a standard visual scanning programme.

Detailed description

In patients with stroke, unilateral neglect is a predictor for poor independency and quality of life. Current therapies are lacking a progression of intensity based on clear criteria. In addition, therapies include rather analytical exercises and the transfer of the achieved functions to activities of daily living remains difficult. Therefore, the investigators developed a criterion based system, in which the investigators are matching interventions to specific neglect related deficits and behaviour. The investigators plan a randomised controlled trial (stage 2 development of concept trial) to evaluate whether an Experimental Group with 20 Sessions of 30 minutes with a visual and tactile scanning training in the personal, peripersonal and extrapersonal space combined with trunk rotation or a Control Group with 20 Sessions of 30 minutes of a standard visual scanning programme results in larger improvements on the neglect behaviour during activities of daily life (Catherine Bergego Scale). Sixteen stroke patients with left side neglect (i.e. right brain lesions) will be recruited in an inpatient rehabilitations setting.

Interventions

OTHERVisual and tactile scanning training

20 Sessions of 30 minutes with a visual and tactile scanning training in the personal, peripersonal and extrapersonal space and trunk rotation. The intervention includes visual or tactile scanning training in three different spaces and will be individually adapted to the needs of the patients. 1. Visual or tactile scanning in the personal space 2. Visual or tactile scanning and trunk rotation in the peripersonal space 3. Visual scanning and trunk rotation in the extrapersonal space

OTHERUni-modal visual scanning training

20 sessions of 30 minutes with traditional uni-modal visual scanning training in the peripersonal space.

Sponsors

University of Applied Sciences of Western Switzerland
CollaboratorOTHER
HES-SO Valais-Wallis
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* First or second time right hemispheric stroke (haemorrhagic or ischaemic, diagnosed with computer tomography or magnetic resonance imaging) * Time after last stroke: less than 8 weeks * Hemispatial neglect with at least seven points on the Catherine Bergego Scale * Right handed

Exclusion criteria

* Reduced vision after rectification (i.e. corrected vision sufficient to read newspaper-sized print) * Mini-Mental State Evaluation Score below 11 * Not fluently speaking and understanding French or German language in order to understand the tasks and the assessments, as assessed and judged by the medical doctor and the staff.

Design outcomes

Primary

MeasureTime frameDescription
Neglect behaviour during activities of daily life measured with the Catherine Bergego Scaleup to 14 monthsMeasured with the Catherine Bergego Scale
Adherence rate of the patients to the treatmentup to 11 months

Secondary

MeasureTime frameDescription
Visual neglect measured with the Behavioural Inattention Test (conventional subtest)up to 14 monthsMeasured with the Behavioural Inattention Test (conventional subtest)
Severity of disability in a rehabilitation setting measured with the Functional Independence Measureup to 11 monthsMeasured with the Functional Independence Measure
Health related quality of life measured with the EQ-5Dup to 14 monthsMeasured with the EQ-5D
Personal neglect measured with the Vest Testup to 14 monthsMeasured with the Vest Test
Inclusion rate and refusal rate per weekup to 11 months
Completeness of documentsup to 11 months
Length of time of assessmentsup to 11 months
Length of stay in inpatient rehabilitation settingup to 11 months
Mobility related disability easured with the Rivermead Mobility Indexup to 11 monthsMeasured with the Rivermead Mobility Index

Countries

Switzerland

Contacts

Primary ContactMartin Sattelmayer, MSc, MA
martin.sattelmayer@hevs.ch
Backup ContactRoger Hilfiker, MPTSc
roger.hilfiker@hevs.ch

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026