The process of drawing blood in a patient ward in a hospital is examined.
Conditions
Interventions
Group 1: This study consists of four different components. The first part involves prospective observation of the blood collection process in a patient ward. The study population consists of patients
Sponsors
Klinikum der Technischen Universität München
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Medical professionals: - All participants are medical professionals (e.g., physicians, nursing assistants, medical students) who are employed at TUM Klinikum before or during the study. - Experience in the relevant field. - Sufficient knowledge of the German language to understand study content and instructions from the scientific staff. - Existing consent to participate in the study. Patients: - Patient with an inpatient treatment contract in surgery. - Sufficient knowledge of German to understand the study content and instructions from the medical staff. - Blood sample collection - Existing consent to participate in the study.
Exclusion criteria
Exclusion criteria: Medical professionals: - Participants have no medical experience at the time of the study. - Participants are not of legal age. Patients: - Belonging to a risk group (age <18 years, psychiatric illness, legal guardianship, pregnancy)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary endpoint is the creation of a process model for blood collection. This is done using observational data from at least 30 patients and is supported by retrospective analysis, workshops, and interviews. The methodology includes prospective observations, retrospective evaluations, semi-structured interviews, and simulations in the form of workshops. | — |
Secondary
| Measure | Time frame |
|---|---|
| Here, further aspects such as ergonomics and hygiene requirements will be considered. | — |
Countries
Germany
Contacts
Public ContactNina Müller
Klinikum der Technischen Universität München
Outcome results
None listed