RECRUITING

PREsurgical Cognitive Evaluation Via Digital clockfacEdrawing

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

PREsurgical Cognitive Evaluation Via Digital clockfacEdrawing

Quick Facts

Study Start:2018-06-28
Study Completion:2026-05-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT03175302

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:65 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * \>/= 65 years of age
  2. * screening within the University of Florida (UF) Health Preoperative clinic
  3. * presurgical cognitive screening with the digital Clock Drawing Tool (dCDT)
  1. * \< 65 years of age
  2. * did not complete screening within the UF Health Preoperative clinic
  3. * did not complete the presurgical cognitive screening with the digital Clock Drawing Tool (dCDT)

Contacts and Locations

Study Contact

Catherine Price, Ph.D.
CONTACT
352-494-6999
cep23@phhp.ufl.edu
Amy Gunnett, RN
CONTACT
352-273-8911
agunnett@anest.ufl.edu

Principal Investigator

Catherine Price, Ph.D.
PRINCIPAL_INVESTIGATOR
University of Florida
Patrick Tighe, MD, MS
PRINCIPAL_INVESTIGATOR
University of Florida

Study Locations (Sites)

UF Health
Gainesville, Florida, 32610
United States

Collaborators and Investigators

Sponsor: University of Florida

  • Catherine Price, Ph.D., PRINCIPAL_INVESTIGATOR, University of Florida
  • Patrick Tighe, MD, MS, PRINCIPAL_INVESTIGATOR, University of Florida

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2018-06-28
Study Completion Date2026-05-31

Study Record Updates

Study Start Date2018-06-28
Study Completion Date2026-05-31

Terms related to this study

Keywords Provided by Researchers

  • cognitive processes
  • perioperative cognition
  • neurocognitive impairment

Additional Relevant MeSH Terms

  • Cognitive Dysfunction