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Neglect Treatment by Prism Adaptation in the Acute Phase

Neglect Treatment by Prism Adaptation in the Acute Phase

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06078111
Acronym
aPA-NEGLECT
Enrollment
32
Registered
2023-10-11
Start date
2023-11-01
Completion date
2026-02-28
Last updated
2024-06-27

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

Conditions

Unilateral Spatial Neglect

Brief summary

This project aims at unveiling the beneficial effects of prism adaptation as early rehabilitation technique to treat unilateral spatial neglect in the acute phase after a brain damage. This syndrome, frequent and very invalidating for daily life activities after a brain damage, is a cognitive disorder of lack of attention towards a part of the space. Patients at a first event brain injury hospitalized into the Neurology and Neurosurgery Departments and affected by spatial neglect will undergo to a protocol of five consecutive rehabilitation treatments, being assigned to the experimental (prisms) or control groups (neutral prisms). The effectiveness of the treatment will be assessed with cognitive, functional and motor-related measures, as well as a follow up 3 months later. These results can have a strong impact on the long-term functional outcome of these patients.

Interventions

BEHAVIORALPrism 10 + visuo-motor activities

Visuo-motor activities of exploration in the left and right space, adapting activities of daily living, while wearing prisms with 10 degrees of visual field deviation

BEHAVIORALNeutral Prism + visuo-motor activities

Visuo-motor activities of exploration in the left and right space, adapting activities of daily living, while wearing prisms with no visual field deviation

Sponsors

University of Geneva, Switzerland
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Caregiver)

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

* First neurological event, affecting the right hemisphere or the left hemisphere (stroke, brain tumour post-surgery); * Structural images of the brain lesion available (magnetic resonance or tomographic scans); * Good Normal (or corrected) visual acuity; * Presence of USN, as assessed by a standard neuropsychological evaluation.

Exclusion criteria

* Previous neurological disorder and/or current or previous psychiatric disease. * Presence or suspicion of previous general cognitive deficits documented from the clinical dossier and/or suspicious of possible cognitive deficits ; * Presence of difficulty in task's comprehension preventing its completion; * Impossibility to sustain a research session of at least 30 minutes (e.g., attentional lability).

Design outcomes

Primary

MeasureTime frameDescription
Unilateral spatial neglectDay 0; Day 5; 12 weeks after the end of the protocolScores in the neuropsychological tasks administered just before and after the rehabilitation protocol: BEN battery, with the number of lateralized omissions in target cancellation, drawing and reading; bisection bias for the line bisection test
Functional measuresDay 0; Day 5; 12 weeks after the end of the protocolScores in the functional test testing USN administered just before and after the rehabilitation protocol: CBS scale, evaluating the impact of neglect in 10 daily living activities (range 0-30)
Disability measuresDay 0; Day 5; 12 weeks after the end of the protocolScale for assessing disability after stroke just before and after the rehabilitation protocol: FIM (range 18-126)
BalanceDay 0; Day 5; 12 weeks after the end of the protocolBalance tests after stroke just before and after the rehabilitation protocol: PASS (range 0-36)

Secondary

MeasureTime frameDescription
Functional Measures: Follow-up12 weeks after the end of the protocolAssessment of the functional benefit of the treatment procedure 3-months after the rehabilitation on the following measure: \- CBS: difference in the total score The difference between patients with spatial neglect who have been submitted to the prism 10 or the neutral prisms protocol will be compared in the follow up. The difference of the scores at the end of the protocol vs. in the follow-up will be performed for each group, and a differential score (prism 10 end of the protocol - prism 10 follow-up vs. neutral prisms end of the protocol - neutral prisms follow-up) will be also analysed to check for the maintenance of the effect. The differences will be computed using the total outcome scores and the incidence (percentage of patients) still defective vs. non-defective at this measure
Neuropsychological tests: Right vs. Left neglectDay 5; 12 weeks after the end of the protocolComparison of the improvements in neuropsychological tests of patients with right vs. left unilateral spatial neglect on the following measures: \- BEN test: numbers of the lateralized omissions left-right in the target cancellation, drawing, reading; bisection bias in the bisection test The difference between patients with right vs. left spatial neglect following brain damaged will be computed by a difference in the outcome scores (omissions rates, bisection biases) and the incidence (percentage of patients) still defective vs. non-defective at each of these measures
Balance: Follow-up12 weeks after the end of the protocolAssessment of the functional benefit of the treatment procedure 3-months after the rehabilitation on the following measure: \- PASS: difference in the total score The difference between patients with spatial neglect who have been submitted to the prism 10 or the neutral prisms protocol will be compared in the follow up. The difference of the scores at the end of the protocol vs. in the follow-up will be performed for each group, and a differential score (prism 10 end of the protocol - prism 10 follow-up vs. neutral prisms end of the protocol - neutral prisms follow-up) will be also analysed to check for the maintenance of the effect. The differences will be computed using the total outcome scores and the incidence (percentage of patients) still defective vs. non-defective at this measure
Functional Measures: Right vs. Left neglectDay 5; 12 weeks after the end of the protocolComparison of the improvements in the functional activities of daily living of patients with right vs. left unilateral spatial neglect on the following measures: \- CBS scale. The difference between patients with right vs. left spatial neglect following brain damaged will be computed by a difference in the outcome scores (total score of the functional scale) and the incidence (percentage of patients) still defective vs. non-defective at this measure
Disability Measures: Right vs. Left neglectDay 5; 12 weeks after the end of the protocolComparison of the improvements of the disability scale of patients with right vs. left unilateral spatial neglect on the following measures: \- FIM The difference between patients with right vs. left spatial neglect following brain damaged will be computed by a difference in the outcome scores (total score of the scale) and the incidence (percentage of patients) still defective vs. non-defective at this measure
Balance: Right vs. Left neglectDay 5; 12 weeks after the end of the protocolComparison of the improvements of balance of patients with right vs. left unilateral spatial neglect on the following measures: \- PASS The difference between patients with right vs. left spatial neglect following brain damaged will be computed by a difference in the outcome scores (total score of the scale) and the incidence (percentage of patients) still defective vs. non-defective at this measure

Countries

Switzerland

Contacts

Primary ContactRoberta Ronchi, PhD
roberta.ronchi@hcuge.ch+41 (0)22 3728314
Backup ContactJennifer Martin, PhD
jennifer.martin@hcuge.ch

Outcome results

None listed

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