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
This trial does not accept healthy volunteersQualifiers
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
Single group
Treatments tested in this trial
custom-created apps, neuropsychological testing, and clinical assessments
Diagnostic testThis study's interventions will include a brief neuropsychological assessment, including pre-operative baseline and post-operative repeat assessment. Additional assessments of memory and coordination using two custom apps and standard clinical assessments will also be conducted at each timepoint
Treatment groups
Trial outcomes
Primary outcomes
Standardized neuropsychiatric testing WAIS SCWT SPWT TOPJ
comparison of results to baseline measurements of these four validated neuropsychiatric assessments
Secondary outcomes
Memory App
Use of a colored sequence presentation memory app to assess subjects return to baseline
Flight Path App
Seated subject follows the flight path of a bird on an iPad app. Comparisons made to baseline performance.
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
This trial is not recruiting at the moment. You can still explore other options: