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Validity and Reliability of the GPCOG -TR

Y

Yeditepe University

Status

Enrolling

Conditions

Dementia

Study type

Observational

Funder types

Other

Identifiers

NCT05704452
GPCOG Validity

Details and patient eligibility

About

The General Practitioner assessment of Cognition (GPCOG) was specifically developed as a brief cognitive screening tool to be used by general practitioners (GPs). It consists of a patient section testing cognition and an informant section asking historical questions. The aim of this study was to test the validity and reliability of the Turkish version of GPCOG-TR on Turkish older adults.

Enrollment

230 estimated patients

Sex

All

Ages

65+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age: least 55 years old
  • Provide informed consent
  • Diagnosed with dementia ( patient group)

Exclusion criteria

  • Living in a nursing home
  • Presence of psychiatric disorders requiring treatment
  • Presence of other comorbidity interfering with cognitive performance such as severe chronic heart failure, chronic obstructive pulmonary disease, diabetes, anemia Impairment of auditory or visual perception
  • Low education
  • Known cognitive impairment (for control group only)
  • Lack of a reliable informant.

Trial design

230 participants in 2 patient groups

Patient group
Description:
who diagnosed with dementia
Control group
Description:
who diagnosed as healthy (don't have dementia)

Trial contacts and locations

1

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Central trial contact

Aber Ahmetoğlu, Master student

Data sourced from clinicaltrials.gov

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