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NCT06042413 · ClinicalTrials.gov registry record · NA
Prediction and Prevention of Postoperative Mortality and Morbidity
A NA study, sponsored by University of Pittsburgh.
- Not yet
- Registry status
- NA
- Development phase
- 1,200
- Enrollment target
NCT06042413 is a NA study that has not yet begun recruiting, run by University of Pittsburgh. The registered enrollment target is 1,200 participants.
The verdict
NCT06042413, a NA study, has not yet begun recruiting, sponsored by University of Pittsburgh.
- NOT YET RECRUITING
- Registry status
- NA
- Development phase
- 1,200 participants
- Enrollment target
Study Summary
This study will contribute to creating a prospective and automated preoperative risk assessment algorithm for predicting 30-day mortality, major adverse cardiac and cerebrovascular events (MACCE), and postoperative neurocognitive outcomes following elective cardiac and vascular surgery in older adults. It will evaluate associations between perioperative factors and longer-term neurocognitive outcomes, including postoperative neurocognitive disorder and dementia. In addition, this study will assess scalable, multimodal preoperative and intraoperative interventions to improve perioperative outcomes. This study will explore two main hypotheses: 1. Preoperative personalized prehabilitation with proactive cognitive and behavioral interventions will improve postoperative cognitive outcomes, morbidity, and mortality in high-risk elderly surgical patients. 2. Proactive bundled intraoperative interventions are superior to reactive standard of care in reducing postoperative cognitive outcomes, MACCE, and mortality. Expected Outcome: Improved EHR algorithm will have higher predictive accuracy for MACCE and mortality while predicting postoperative cognitive outcomes.
Interventions
- BEHAVIORAL Cognitive Training
- BEHAVIORAL Meditation
- OTHER Personalized CPC Prehabilitation
- BEHAVIORAL Daily Exercise
- BEHAVIORAL Enhanced Social Support
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 1,200 participants |
| Start Date | 2026-08 |
| Est. Completion | 2027-06 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06042413
The ClinicalTrials.gov registry entry for NCT06042413 describes a study currently listed as not yet recruiting, categorized as NA. The registered enrollment target is 1,200 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Pittsburgh, which has 1,238 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 5 interventions - of which Cognitive Training is the first listed.
NCT06042413 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT06042413 about?
NCT06042413 is a clinical study titled "Prediction and Prevention of Postoperative Mortality and Morbidity". This study will contribute to creating a prospective and automated preoperative risk assessment algorithm for predicting 30-day mortality, major adverse cardiac and cerebrovascular events (MACCE), and postoperative neurocognitive outcomes following elective cardiac and vascular surgery in older adul...
What is the current status of trial NCT06042413?
This trial is currently not yet recruiting. It is a NA study. The enrollment target is 1,200 participants. The study started on 2026-08. Estimated completion is 2027-06.
What interventions are being tested in trial NCT06042413?
The interventions under investigation include: Cognitive Training (BEHAVIORAL), Meditation (BEHAVIORAL), Personalized CPC Prehabilitation (OTHER), Daily Exercise (BEHAVIORAL), Enhanced Social Support (BEHAVIORAL).
Who is sponsoring clinical trial NCT06042413?
This trial is sponsored by University of Pittsburgh, which has 1,238 total clinical trials registered on ClinicalTrials.gov.
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