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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02204787
Other study ID # 9257
Secondary ID
Status Completed
Phase Phase 1/Phase 2
First received
Last updated
Start date April 1, 2014
Est. completion date October 26, 2018

Study information

Verified date November 2017
Source University Hospital, Montpellier
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this study is to evaluate the therapeutic efficacy of a neuromodulation technique, tDCS (transcranial direct current stimulation) used as a complementary treatment on negative symptoms. 60 patients will be randomized into two groups (active tDCS vs sham tDCS) and will be assessed after the intervention, 1 and 3 months after.Secondary outcomes shall include neuropsychological assessment, general symptomatology, extrapyramidal symptoms and social functioning.


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date October 26, 2018
Est. primary completion date October 26, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years to 60 Years
Eligibility - Inclusion Criteria: - Schizophrenia with prominent negative symptoms - Exclusion Criteria: - other psychiatric or neurological diseases - specific tDCS limitations

Study Design


Related Conditions & MeSH terms


Intervention

Device:
transcranial direct current stimulation


Locations

Country Name City State
France UH Montpellier Montpellier

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Montpellier

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Scale for the Assessment of Negative Symptoms up to 3 months after intervention
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