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Validation of The Telephone Interview for Cognitive Status and Montreal Cognitive Assessment against neuropsychological assessment for postoperative cognitive dysfunction in the elderly (The TINMAN study).

Completed
Conditions
memory loss after surgery
Postoperative Cognitive Disorder
10009841
Registration Number
NL-OMON48512
Lead Sponsor
Academisch Medisch Centrum
Brief Summary

Trial is onging in other countries

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
105
Inclusion Criteria

In order to be eligible to participate in this study, a patient must meet all
of the following criteria:
- Elective minor, moderate or major surgery, according to the definition of the
European Society of Anesthesiology
- Age *65 years
- ASA l - lV
- Fluent in written and spoken Dutch
- Willing and able to undergo neuropsychological assessment, and have the MoCA
and TICS administered both pre- and approximately one month postoperatively.

Exclusion Criteria

- Emergency surgery
- Previously diagnosed cognitive dysfunction
- Patients who are unable to understand or fill-in questionnaires in Dutch

Study & Design

Study Type
Observational non invasive
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<p>- Agreement between performance on the TICS, MoCA and NPA and its cognitive<br /><br>domains<br /><br>o The correlation between the TICS, MoCA and total NPA score and baseline<br /><br>characteristics<br /><br>o The correlation between the TICS, MoCA and the cognitive domain scores of the<br /><br>NPA and baseline characteristics<br /><br>o The correlation between TICS and MoCA total scores and cognitive domain<br /><br>scores pre- and approximately one month postoperatively</p><br>
Secondary Outcome Measures
NameTimeMethod
<p>- The validity, sensitivity and specificity of the TICS and MoCA questionnaires<br /><br>compared to the gold standard (NPA) both on baseline and on postoperative<br /><br>change scores from baseline</p><br>
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