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

• Conditions: dementia; 10042258

• Registration Number: NL-OMON33824
• Lead Sponsor: Academisch Medisch Centrum

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 6 May 2024

Recruitment & Eligibility

• Status: Pending
• Sex: Not specified
• Target Recruitment: 84

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

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

Study & Design

• Study Type: Observational non invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>Duration of cognitive testing using CAT in comparison with the test duration of<br /><br>the CAMCOG.<br /><br>Diagnostic accuracy of cognitive testing CAT in comparison with conventional<br /><br>cognitive testing (i.e. administering a fixed set of items to every patient). </p><br>

Secondary Outcome Measures

Name	Time	Method
<p>-</p><br>