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Clinical Trials/NCT02506075
NCT02506075
Unknown
N/A

Effectiveness of Transcranial Direct Current Stimulation for Unilateral Neglect After Stroke

Pusan National University1 site in 1 country105 target enrollmentApril 2015
ConditionsStroke

Overview

Phase
N/A
Intervention
Not specified
Conditions
Stroke
Sponsor
Pusan National University
Enrollment
105
Locations
1
Primary Endpoint
Behavioral Inattention Test
Last Updated
10 years ago

Overview

Brief Summary

The primary objective of this study is to confirm and compare the effect of methods of transcranial direct current stimulation(tDCS) in the unilateral neglect of stroke patients

Detailed Description

Total 105 patients were recruited and randomized to receive either real or sham-tDCS. Real experimental groups were divided into two types; Pre-tDCS group and Simultaneous tDCS group. Two groups are again divided into three groups; Dual stimulation group, Unilateral stimulation group and Sham control group, respectively. In Pre-tDCS group, total a sessions of the tDCS stimulation was done for each three subgroups and visual inattention training was followed after that. In Simultaneous tDCS group, tDCS and visual inattention training was done simultaneously. For each subgroups, tDCS was attached at following locations; unilateral cathodal tDCS on unaffected PPC(postparietal cortex), P3 , dual cathodal tDCS on P3 and anodal tDCS on affected PPC, P4. The patients were initially evaluated at baseline, immediately, 60min, 120min, 24 hrs after the training session.

Registry
clinicaltrials.gov
Start Date
April 2015
End Date
February 2016
Last Updated
10 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Yong-il Shin

Associate Professor

Pusan National University

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Behavioral Inattention Test

Time Frame: up to 2 min

Letter cancellation test

Secondary Outcomes

  • ADL assssement(60 min, 120 min, 24 hrs after intervention)
  • Behavioral Inattention Test(60 min, 120 min, 24 hrs after intervention)

Study Sites (1)

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