PREsurgical Cognitive Evaluation Via Digital clockfacEdrawing

Recruiting Observational Study
Cognitive Dysfunction
No Placebo Group Every participant receives an active treatment — no one gets a placebo. No Study Drug Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Age
65 and older
Sex
Any
Study type
Observational
Participants needed
25,240 (estimated)
Sponsor
University of Florida · Other
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About This Trial

This study leverages a modernized digital version of a well-known cognitive screening tool to examine pre and post operative cognitive function after surgery in adults age 65 years or more. Machine learning algorithms will be applied to the hospital wide standard of care cognitive metric to identify risk for post-operative cognitive complications.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * \>/= 65 years of age * screening within the University of Florida (UF) Health Preoperative clinic * presurgical cognitive screening with the digital Clock Drawing Tool (dCDT) Exclusion Criteria: * \< 65 years of age * did not complete screening within the UF Health Preoperat…
Contacts

Catherine Price, Ph.D.

352-494-6999

cep23@phhp.ufl.edu

CONTACT

Amy Gunnett, RN

352-273-8911

agunnett@anest.ufl.edu

CONTACT