ClinicalTrials.Veeva

Menu

Prismatic Lenses and tDCS in Neglect

I

Istituti Clinici Scientifici Maugeri SpA

Status

Enrolling

Conditions

Stroke, Ischemic

Treatments

Combination Product: Prismatic adaptation and electric stimulation

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

The goal of this study is to to evaluate the effect and feasibility of a rehabilitation protocol with prismatic lenses associated with tDCS, compared to a prismatic lens rehabilitation protocol associated with sham stimulation, in reducing the signs of neglect in a group of patients with spatial heminegligence following ischemic stroke of the right hemisphere.

The secondary objective is to evaluate the impact of this rehabilitation protocol on functional outcome.

Enrollment

30 estimated patients

Sex

All

Ages

18 to 90 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • age >18 years
  • ischemic stroke
  • hospitalization within 90 days of the event

Exclusion criteria

  • heamorrhagic stroke
  • history of neurological disease
  • history of psychiatric disease
  • use of alchool and drugs

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

30 participants in 2 patient groups

Experimental
Experimental group
Description:
Patients will receive anodic tEs combined with prismatic lenses for two weeks
Treatment:
Combination Product: Prismatic adaptation and electric stimulation
Control
Sham Comparator group
Description:
Patients will receive sham tEs combined with prismatic lenses for two weeks
Treatment:
Combination Product: Prismatic adaptation and electric stimulation

Trial contacts and locations

1

Loading...

Central trial contact

Simona Spaccavento

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems