- Conditions
- Dementia, Major Adverse Cardiac and Cerebrovascular Events, Perioperative Complications, Postoperative Cognitive Decline, Postoperative Delirium (POD), Postoperative Neurocognitive Disorder
- Interventions
- Cognitive Training, Daily Exercise, Enhanced Social Support, Intra-operative Standard of Care, Meditation, Personalized CPC Prehabilitation, Pre-operative Standard of Care, Proactive Bundle Interventions
- Behavioral · Procedure · Other
- Lead sponsor
- University of Pittsburgh
- Other
- Eligibility
- 65 Years and older
- Enrollment
- 1,200 participants
- Healthy volunteers
- Healthy volunteers not accepted
- Timeline
- 2026 – 2027
- U.S. locations
- 5
- States / cities
- Pittsburgh, Pennsylvania
Source: ClinicalTrials.gov public record
Updated Apr 13, 2026 · Synced May 19, 2026, 10:53 AM EDT