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Clinical Trials/NCT05842551
NCT05842551
Recruiting
Not Applicable

The Effect of Prismatic Lenses in Association With tDCS in Patients With Neglect: a Pilot Study

Istituti Clinici Scientifici Maugeri SpA1 site in 1 country30 target enrollmentMarch 7, 2023

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Stroke, Ischemic
Sponsor
Istituti Clinici Scientifici Maugeri SpA
Enrollment
30
Locations
1
Primary Endpoint
Neuropsychological outcome
Status
Recruiting
Last Updated
7 months ago

Overview

Brief Summary

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.

Registry
clinicaltrials.gov
Start Date
March 7, 2023
End Date
December 31, 2026
Last Updated
7 months ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Simona Spaccavento

Principal Investigator

Istituti Clinici Scientifici Maugeri SpA

Eligibility Criteria

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

Outcomes

Primary Outcomes

Neuropsychological outcome

Time Frame: Change from baseline the Bergegò Scale at 2 weeks.

Bergegò Scale (0-30); high score means a better outcome

Functional outcome

Time Frame: Change from baseline the Barthel Index at 2 weeks

Barthel Index (0-100); high score means a better outcome

Study Sites (1)

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