Actively Recruiting

Age: 18Years - 65Years
All Genders
NCT06278532

Validation of the Lithuanian Version of the BNSS, CDSS, and the SCoRS

Led by Lithuanian University of Health Sciences · Updated on 2024-02-26

200

Participants Needed

2

Research Sites

156 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study aims to validate the Lithuanian version of the Brief Negative Symptoms Scale, Calgary Depression Scale for Schizophrenia, and Schizophrenia Cognition Rating Scale in a Lithuanian sample. This will be done by comparing results obtained from the Brief Negative Symptoms Scale, Calgary Depression Scale for Schizophrenia, and Schizophrenia Cognition Rating Scale with results obtained from the Positive and Negative Symptoms Scale, the Montgomery Asberg Depression Rating Scale, and the Montreal Cognitive Assessment test.

CONDITIONS

Official Title

Validation of the Lithuanian Version of the BNSS, CDSS, and the SCoRS

Who Can Participate

Age: 18Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 to 65 years old
  • Diagnosis of F20, F25, or F21 according to ICD-10
  • Signed informed consent form
Not Eligible

You will not qualify if you...

  • Younger than 18 or older than 65 years old
  • Did not sign the informed consent form
  • Legally inactive person
  • Diagnosis of mental retardation (F70 - F79) according to ICD-10
  • Diagnosis of mental and behavioural disorders due to psychoactive substance use (F10 - F19)
  • Diagnosis of organic, including symptomatic, mental disorders (F00 - F09)

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 2 locations

1

Lithuanian University of Health Sciences Hospital Kaunas Clinics

Kaunas, Lithuania, LT-50161

Actively Recruiting

2

Jonas Montvidas

Kaunas, Lithuania, LT-53137

Actively Recruiting

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Research Team

J

Jonas Montvidas, MD

CONTACT

A

Algirdas Musneckis, MD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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