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Control for Cognitive Impairment (PRECEDE Trial)
N/A
Recruiting
Led By Catherine Price, Ph.D.
Research Sponsored by University of Florida
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to one year
Awards & highlights
Summary
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.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ up to 1 year
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 1 year
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Control and pre-surgery differences between digital behaviors
Secondary outcome measures
Change over time in digital behavior between groups
Predictive validity of digital behaviors on outcome
Trial Design
2Treatment groups
Experimental Treatment
Group I: Surgical groupExperimental Treatment1 Intervention
Baseline preoperative digital cognitive testing performance in adults to predict frequency and severity of clinician reported outcomes within the first three months post-surgery.
Group II: ControlExperimental Treatment1 Intervention
Non-surgery matched peers with the same testing.
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Who is running the clinical trial?
University of FloridaLead Sponsor
1,380 Previous Clinical Trials
737,155 Total Patients Enrolled
National Institute on Aging (NIA)NIH
1,733 Previous Clinical Trials
28,029,763 Total Patients Enrolled
National Center for Advancing Translational Sciences (NCATS)NIH
342 Previous Clinical Trials
385,228 Total Patients Enrolled
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