Improving quality of life for patients undergoing urological surgery
Standardized Collection of Patient Reported Outcomes (PROs) in Everyday Clinical Practice
Medical University of Graz · NCT06397287
This study is testing whether using personalized questionnaires can help improve the quality of life and recovery for patients having urological surgery.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 47 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Medical University of Graz (other) |
| Locations | 1 site (Graz, Styria) |
| Trial ID | NCT06397287 on ClinicalTrials.gov |
What this trial studies
This observational study aims to enhance the quality of care for patients undergoing urological surgery by implementing standardized questionnaires that assess quality of life, satisfaction, pain, and physical recovery. Patients will receive individualized treatment pathways based on their specific conditions, such as localized prostate cancer or benign prostate enlargement. The collected data will be used to improve clinical outcomes and tailor treatment approaches to better meet patient needs.
Who should consider this trial
Good fit: Ideal candidates include adults aged 18 and older who are undergoing treatment at the Department of Urology and can provide informed consent.
Not a fit: Patients who lack digital competence or cannot provide written consent may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could lead to improved patient satisfaction and recovery outcomes after urological surgeries.
How similar studies have performed: Other studies have shown success in using patient-reported outcome measures to enhance treatment pathways, indicating a promising approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Patients treated at the Department of Urology 2. ≥18 years of age 3. Active Mail-account, use of smartphone/tablet/PC 4. Written informed consent Exclusion Criteria: \- Patients who cannot give written consent and/or do not have digital competence (e.g. no active e-mail account)
Where this trial is running
Graz, Styria
- Röthl Martina Anna — Graz, Styria, Austria (RECRUITING)
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Surgery, Urologic Diseases, Urologic Cancer