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PAPSY - Memory in Psychiatry

C

Charles University, Czech Republic

Status

Active, not recruiting

Conditions

Cognitive Impairment

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

Memory in Psychiatry project (PAPSY) aims to map the distribution and severity of cognitive impairment in patients of outpatient psychiatric offices across the geographical area of the Czech Republic. 1000 patients in 90 psychiatric offices will undergo cognitive tests (ALBA and PICNIR) and psychometric scales (sFAQ-CZ and GDS-CZ) to asses their functional state and depressive symptoms. If applicable, caretakers will also be asked about the extent of the participant's autonomy and behavioral impairment (using oFAQ-CZ and MBI-C-CZ scales).

The trial's primary goal is to assess the distribution of cognitive impairment among diagnostic groups in psychiatric care according to the ICD-10. Additionally, the feasibility of ALBA and PICNIR methods to uncover previously undiagnosed cognitive impairments will be evaluated.

Enrollment

1,000 estimated patients

Sex

All

Ages

45+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Dispensarization of at least six months in an outpatient psychiatric office with an ICD-10 diagnosis
  • Age>=45
  • Permanent residency in the geographical area of the Czech Republic

Exclusion criteria

  • Diagnosis of mental retardation (F70-F79) according to ICD-10
  • Refusal to sign the informed consent and consent with GDPR
  • Uncorrected visual impairment
  • Uncorrected auditory impairment
  • Inability to participate in the project

Trial design

1,000 participants in 1 patient group

Observed group
Description:
No intervention will be administered on behalf of the project. The participants will be tested using ALBA and PICNIR (non-invasive) cognitive tests, and further sFAQ-CZ and GDS-CZ questionnaires will be administered. Questionnaires FAQ-CZ and MBI-C-CZ will be distributed to participants´ caretakers.

Trial contacts and locations

1

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Central trial contact

Aleš Bartoš, M.D., Ph.D.; Tadeáš Mareš, M.D.

Data sourced from clinicaltrials.gov

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