N/A
Completed N=586
Developing and Testing a Personalized Evidence-based Shared Decision-making Tool for Stent Selection
Source: ClinicalTrials.gov NCT02046902 ↗Enrolled (actual)
586
Serious AEs
—
Results posted
Jul 2019
Primary outcomePrimary: Assessment of Pre-implementation, Post-implementation With Decision Coaching, and Post-implementation Without Decision Coaching — 235; 45; 106; 51 Participants
Summary
The goal of this study is to gather input from patients who have undergone PCI, their family and/or caregivers, and clinicians to develop a patient decision aid. The purpose of the decision aid is to deliver information, including individualized estimates of patients' restenosis risk, in an understandable format that would be informative and assist in decision-making for patients undergoing PCI.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Assessment of Pre-implementation, Post-implementation With Decision Coaching, and Post-implementation Without Decision Coaching |
235; 45; 106; 51; 19; 20 | — |
| SECONDARY Concordance Between Stent Preference and Stent Received Was a Secondary Outcome. |
83; 49; 23; 36; 29; 2 | — |
Eligibility Criteria
Inclusion Criteria
- >18 years old
- English or Spanish speaking
- Presence of coronary disease, or a caregiver/relative of one with coronary disease
Exclusion Criteria
- non-English or non-Spanish speaking
- dementia
Data sourced from ClinicalTrials.gov (NCT02046902). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.