Predicting Depressive Symptoms After Heart Bypass Surgery
Builds a model to identify adults at risk of depression after bypass surgery.
Plain-language title generated from the registry record
Registry title: Depressive Symptoms After Cardiac Surgery
Key facts
- Where
- Zurich, SwitzerlandSee the 2 sites
Could this be for you?
Answer for yourself. This is not a decision: only the study team can say whether you can take part.
- Are you between 18 and 90 years old?
Source: NCT06706323, who can take part
Where in Switzerland
- Stadtspital Zürich (City Hospital Zurich) TriemliZurich, SwitzerlandTaking people
- University Hospital Zurich (USZ)Zurich, SwitzerlandNot yet recruiting
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Trial details
- Who runs it
- Roland von Känel
- Trial code
- NCT06706323
- Record updated
- 1 April 2025
- Original description
The primary goal of this project is to develop a predictive model for clinically significant depressive symptoms (CSDS) in patients undergoing coronary artery bypass graft (CABG) surgery, using pre- and perioperative data. CSDS occur in about 30 percent of CABG patients, which is four times higher than in the general population. These symptoms are linked to poor quality of life and increased morbidity and mortality. The aim is to create a model that can identify patients at risk for postoperative depression. This tool could help clinicians make informed decisions and take preventive measures to manage depression after surgery.Read full original descriptionShow less
Predictive Modelling of Clinically Significant Depressive Symptoms After Coronary Artery Bypass Graft Surgery
The primary goal of this project is to develop a predictive model for clinically significant depressive symptoms (CSDS) in patients undergoing coronary artery bypass graft (CABG) surgery, using pre- and perioperative data. CSDS occur in about 30 percent of CABG patients, which is four times higher than in the general population. These symptoms are linked to poor quality of life and increased morbidity and mortality. The aim is to create a model that can identify patients at risk for postoperative depression. This tool could help clinicians make informed decisions and take preventive measures to manage depression after surgery.
Inclusion: Elective Off-Pump CABG or CABG, either isolated or combined with valve intervention; Men and women, aged between 18 and 90 years; Sufficient knowledge of German language in reading and understanding; Oral and Signed consent form; Ability and Willingness to follow the study protocol.
Exclusion: Cognitive impairment according to a score of ≤ 7 (maximum score = 9) on a modified version of a short version of the Mini-Mental State Examination and the Brief Interview for Mental Status; Any serious comorbid non-cardiac medical condition likely to cause death within 1 year (e.g. metastatic cancer); Active psychotic symptoms (assessed with two items from the Youth Psychosis At Risk Questionnaire), substance abuse and/or dependence within the past 6 months (assessed with a single-item questionnaire), and/or active suicidal ideations (assessed with a single item from the M.I.N.I.); Acute or emergency CABG.