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PREsurgical Cognitive Evaluation Via Digital clockfacEdrawing (PRECEDE)

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University of Florida

Status

Enrolling

Conditions

Cognitive Dysfunction

Treatments

Behavioral: digital cognitive testing

Study type

Observational

Funder types

Other
NIH

Identifiers

NCT03175302
IRB201700747-N
OCR18881 (Other Identifier)
R01AG055337 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

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.

Full description

This proposal innovatively leverages a brief but informative digital test with machine learning to examine the subtlety of pre-surgery cognition within an extremely large number of older individuals screened preoperatively within an academic tertiary medical center. It also incorporates a unique group of well characterized non-surgery peers for demographic matching to assist with normal versus abnormal machine learning analyses.

Enrollment

25,240 estimated patients

Sex

All

Ages

65+ years old

Volunteers

No Healthy Volunteers

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 Preoperative clinic
  • did not complete the presurgical cognitive screening with the digital Clock Drawing Tool (dCDT)

Trial design

25,240 participants in 2 patient groups

Surgical group
Description:
Baseline preoperative digital cognitive testing performance in adults to predict frequency and severity of clinician reported outcomes within the first three months post-surgery.
Treatment:
Behavioral: digital cognitive testing
Control
Description:
Non-surgery matched peers with the same testing.
Treatment:
Behavioral: digital cognitive testing

Trial contacts and locations

1

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Central trial contact

Amy Gunnett, RN; Catherine Price, Ph.D.

Data sourced from clinicaltrials.gov

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