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).
- Conditions
- memory loss after surgeryPostoperative Cognitive Disorder10009841
- 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
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.
- 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
Name Time Method <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
Name Time Method <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>