PACU Discharge Readiness
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorUniversity of Illinois at Chicago
About this trial
The use of custom-created apps, neuropsychological testing, and clinical assessments will be evaluated as tools for determining the appropriateness of PACU discharge to home.
Eligibility criteria
Qualifiers
The individuals will be identified from the operating room (OR) schedule and approached in the pre-operative area (or earlier, when possible).
Adult patients (18 years or older) listed for surgery and a planned 23-hour admission will be eligible for enrollment in this study.
Subjects must be fluent in English and not have confounding sensory or neurological limitations to participation
Disqualifiers
Members of vulnerable populations or adults unable to consent will be included in this study.
Subjects that do not speak English
Subjects with neurological limirations
Trial design
Treatments tested in this trial
- custom-created apps, neuropsychological testing, and clinical assessments
Treatment groups
1,000 Participants
are divided into 1 treatment groupLocations
1University of Illinois Chicago60612, ChicagoIllinois, United States
Sponsors and collaborators
University of Illinois at Chicago
Lead sponsor
Source ClinicalTrials.gov