Basic↦Statistic Methodology↦Research Question↦Outcome Endpoint Description
Was betrifft es? Warum ist das wichtig?
Study outcomes/endpoints are variables that are medical values or information of interest to a researcher to address the research question.
As any variable, study outcome/endpoint variables, can be of different types, such as:
- Continuous variables (e.g. weight, lab values such as cholesterol-, blood pressure values)
- Categorical variables (e.g. such as the categorisation into bad/normal/good)
- Binary variables (e.g. expressed as binary categories such as, dead/alive, yes/no, normal/abnormal, accepted/rejected)
- Count variables (e.g. number of hospital visits)
- Time-to-event variables (e.g. time to initial cardiovascular event)
Was muss ich befolgen?
As a SP-INV, make yourself familiar with how to define your study outcome/endpoint variables. Aspects to include are:
- A precise definition of the outcomes type. For example, if you are interested in re-hospitalization: do you want to draw conclusions about the occurrence (yes or no), the number as a count or as categories (e.g., 0, 1 to 3, more than 3), the time relapsed until the first re-hospitalization?
- The definition of the time point of interest: are you interested in any re-hospitalization occurring in the first 3 months after surgery, or the “number of re-hospitalizations” during a 2 year follow-up?
Wo kann ich Hilfe anfordern?
Your local Research Support Centre↧ can assist you with experienced staff regarding this topic
Basel, Departement Klinische Forschung (DKF), dkf.unibas.ch
Lugano, Clinical Trials Unit (CTU-EOC), ctueoc.ch
Bern, Department of Clinical Research (DCR), dcr.unibe.ch
Geneva, Clinical Research Center (CRC), crc.hug.ch
Lausanne, Clinical Research Center (CRC), chuv.ch
St. Gallen, Clinical Trials Unit (CTU), h-och.ch
Zürich, Clinical Trials Center (CTC), usz.ch
References
ICH Topic E9 statistical Principles for Clinical Trials – see in particular
- 2.2.2 Primary and secondary variables
- 2.2.5 Multiple Primary Variables