C67
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Confirmed diagnosis of bladder cancer, membership in a support group or contact through such a group, sufficient knowledge of German, capacity to give consent
Exclusion criteria
Exclusion criteria: Incapacity to give consent, insufficient knowledge of German, no diagnosis of bladder cancer
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. Quantitative assessment of patient-reported distress during cystoscopy, including various dimensions of distress (e.g., pain during/after the examination, burning sensation when urinating, shame, anxiety/stress before the appointment, concern about the results, feeling of loss of control/helplessness, organizational effort); using a visual analog scale (VAS, 0–10) 2. Assessment of the importance of research into non-invasive alternatives to cystoscopy from the patient's perspective; recorded using a five-point Likert scale from unimportant to very important | — |
Secondary
| Measure | Time frame |
|---|---|
| 1.Rate of adverse side effects (urinary tract infections, bleeding, persistent pain among respondents) following cystoscopy; recorded using relative frequencies 2. Survey of examination conditions: percentage of rigid vs. flexible cystoscopies and percentage of different forms of anesthesia 3. Rate of psychological stress (sleep disorders, depression) in the context of follow-up care; recorded using relative frequencies 4. Participants' confidence in AI-supported urine cytology compared to evaluation by a physician (preference indicated: physician alone vs. AI alone vs. combination); recorded once using a questionnaire 5. Collection of additional follow-up care-related information, e.g., percentage of wearers of various urinary tract devices, percentage of patients who were offered a structured smoking cessation program | — |
Countries
Germany
Contacts
Klinik für Urologie und Urochirurgie Universitätsmedizin Mannheim