RecruitingNot ApplicableNCT05373017

Delirium and Neuropsychological Recovery Among Emergency General Surgery Survivors

Delirium and Neuropsychological Recovery Among Emergency General Surgery Survivors (DANE)


Sponsor

University of Wisconsin, Madison

Enrollment

528 participants

Start Date

Feb 13, 2023

Study Type

INTERVENTIONAL

Conditions

Summary

This study will evaluate the usefulness of the Urgent and Emergency Surgery (UES) Delirium Recovery Model. It is hypothesized that the cognitive, physical and psychological recovery of older UES delirium survivors will be improved through the use of the DANE Recovery Model. Participants can expect to be on the study for 18 months.


Eligibility

Min Age: 65 Years

Inclusion Criteria8

  • Adult age 65 years and older
  • Admitted to one of the participating hospitals
  • Undergone an abdominal orthopedic, skin, or vascular surgery in an emergency or unplanned fashion
  • English-speaking
  • Able to provide consent or have a legally authorized representative to provide consent
  • Access to a telephone or an internet connected computer or smart device
  • Discharged to home or sub-acute rehabilitation
  • At least one episode of delirium or subsyndromal delirium, i.e. screen positive on at least one out of the four items on the Confusion Assessment Method-ICU (CAM-ICU) in the period prior to discharge from acute care.

Exclusion Criteria7

  • A self-reported diagnosis of cancer with short life expectancy
  • A history of dementing illnesses and other neurodegenerative disease such as Alzheimer's disease (AD), Parkinson disease, or vascular dementia, or current prescription of anti-dementia medication, or ruled out by Functional Activities Questionnaire (FAQ) score defining dementia; a history of significant traumatic brain injury
  • Acute or subacute neurologic deficit expected to prevent independent living after hospital discharge, e.g., a history of a significant traumatic brain injury
  • Have any spinal cord injury with persistent neurologic deficit at the time of study enrollment
  • Incarcerated or homeless at the time of study enrollment
  • Acquired neurologic injury (stroke, traumatic brain injury, cerebral edema/swelling, anoxic brain injury, or any other acute/subacute severe neurologic deficit) as the admitting diagnosis or a new event during the course of hospitalization (confirmed by EMR)
  • A history of bipolar disorder or schizophrenia (confirmed by EMR)

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

OTHERDANE Recovery Program

Virtual visits with care coordinator to carry out an individualized recovery plan

OTHERQuestionnaires

Physical, cognitive, and psychological assessments


Locations(6)

SwedishAmerican Hospital

Rockford, Illinois, United States

Indiana University

Indianapolis, Indiana, United States

University of Wisconsin

Madison, Wisconsin, United States

Meriter Hospital

Madison, Wisconsin, United States

East Madison Hospital

Madison, Wisconsin, United States

Medical College of Wisconsin

Milwaukee, Wisconsin, United States

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT05373017


Related Trials