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Tailoring the screening for cognitive impairment to the individual patient with Computerised Adaptive Testing (CAT)

Tailoring the screening for cognitive impairment to the individual patient with Computerised Adaptive Testing (CAT) - Computerised Adaptive Testing

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON33824
Enrollment
84
Registered
2009-02-06
Start date
2008-11-01
Completion date
Unknown
Last updated
2024-05-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

dementia

Interventions

None listed

Sponsors

Academisch Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Patients visiting a neurologic outpatient clinic / memory clinic with memory complaints and other cognitive disorders who are suspected of dementia and who were consecutively referred by their GP or family physician.

Exclusion criteria

Exclusion criteria: Patients and spouses / relatives with insufficient vision, audition, paresis of dominant hand, insufficient command of Dutch are excluded. In addition spouses / relatives who see the patient less than once a week or who are demented themselves. No informed consent

Design outcomes

Primary

MeasureTime frame
Duration of cognitive testing using CAT in comparison with the test duration of the CAMCOG. Diagnostic accuracy of cognitive testing CAT in comparison with conventional cognitive testing (i.e. administering a fixed set of items to every patient).

Secondary

MeasureTime frame
-

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)