Completed

POCDCohort Study of Risk Factors for Postoperative Cognitive Decline

0 criteria met from your profileSee at a glance how your profile meets each eligibility criteria.
What is being collected

Data Collection

Collected from today forward - Prospective
DNA Samples
Who is being recruted

Mental Disorders+1

+ Cognition Disorders

+ Neurocognitive Disorders

From 65 to 89 Years
+12 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Cohort

Tracking disease incidence in order to identify risk factors and understand disease progression over time.
Observational
Study Start: March 2018
See protocol details

Summary

Principal SponsorOregon Health and Science University
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: March 26, 2018

Actual date on which the first participant was enrolled.

Adults 65 years and older represent the fastest-growing age group in the United States, and account for one third of all surgical patients. These older adults are at the highest risk for deleterious postoperative neurocognitive outcomes. Postoperative cognitive dysfunction (POCD) occurs in up to 40% of older adults after major non-cardiac surgery. POCD is a syndrome characterized by a decrease in performance on neuropsychological test battery from before to after surgery. Neuropsychological testing for POCD typically spans cognitive domains including memory, attention, concentration, and/or executive function. There is an increasing body of literature suggesting that exposure to surgery and anesthesia increases the risk of Alzheimer's disease (AD). Surgery and anesthesia enhance neuropathologic changes known to underlie AD including amyloid beta accumulation and aggregation, neuroinflammation, increased levels of tau and tau phosphorylation, and memory decline. However, not everyone with a history of surgery and anesthesia develops POCD, suggesting biological risk factors are involved.

Official TitleCohort Study of Risk Factors for Postoperative Cognitive Decline
Principal SponsorOregon Health and Science University
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

125 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Cohort

These studies follow a group of individuals with common characteristics (such as a condition or birth year) over a specific period to study health outcomes or exposures.


Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

From 65 to 89 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Mental DisordersCognition DisordersNeurocognitive DisordersCognitive Dysfunction

Criteria

4 inclusion criteria required to participate
Scheduled for an in-patient, elective spine surgery where subject will receive general anesthesia

Presenting to spine clinic and undergoing conservative, non-surgical management of spine disorder

Subjects must have sufficient vision and hearing to complete neuropsychological testing

Proficient in spoken and written English language

8 exclusion criteria prevent from participating
Refusal of consent

Diagnosed dementia or dementia-related treatment (i.e. donepezil prescription, or memory-care facility residence)

Significant disease of the central nervous system (CNS) (i.e. Parkinson's disease)

History of stroke or traumatic brain injury

Show More Criteria

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Study Objectives

Study Objectives

Primary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Suspended

OHSU

Portland, United StatesOpen OHSU in Google Maps
CompletedOne Study Center