Prostate cancer
Conditions
Interventions
No grouping is applied to the prediction model section of this study.:None
No grouping is applied to the qualitative interview section of this study.:None
Sponsors
Fudan University Cancer Hospital
Eligibility
Sex/Gender
Male
Age
18 Years to 85 Years
Inclusion criteria
Inclusion criteria: 1. Prediction Model Section: (1) Pathological diagnosis of prostate cancer confirmed by prostate biopsy or transurethral prostatectomy before surgery; (2) Age >= 18 years old; (3) Intending to undergo laparoscopic radical prostatectomy (LRP) or robot-assisted laparoscopic radical prostatectomy (RARP) at our hospital; (4) Able to tolerate the surgery and have no contraindications; (5),; (6) Willing to participate in this study and sign the informed consent form. 2. Qualitative Research Section: (1) Medical Staff: 1) Engaged in clinical work in urology, pelvic floor rehabilitation department, or prostate cancer specialty, with clinical practice or guidance experience in pelvic floor rehabilitation for patients after radical prostatectomy (RP); 2) Intermediate or above professional title, and having worked continuously in urology or related fields for >= 5 years; 3) Possessing clear logical expression ability, without communication barriers, and able to fully participate in semi-structured interviews; 4) Fully understand the purpose and process of this study, voluntarily sign the informed consent form and participate in this study. (2) Patients: 1) Patients who have undergone radical prostatectomy for prostate cancer and are currently receiving or planning to initiate pelvic floor rehabilitation; 2) Age >= 18 years old, without communication barriers or mental disorders; 3) Fully understand the purpose and process of this study, voluntarily sign the informed consent form and participate in this study.
Exclusion criteria
Exclusion criteria: 1. Prediction model section: (1) Patients with other malignant tumors; (2) Those with cognitive impairment, mental illness or language communication disorders, unable to complete the scale assessment; (3) With incomplete clinical data or refusing follow-up; (4) Those with surgical conversions to open surgery or who stopped the surgery. 2. Qualitative research section: (1) Medical staff: 1) Clinical intern medical students, visiting physicians or nurses, and staff at the stage of standardized training; 2) Those who cannot complete the complete interview for various reasons or refuse to provide the clinical practice information required for the interview. (2) Patients: 1) Those at the terminal stage of the disease with critical conditions; 2) Those who cannot communicate in Mandarin.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Incidence of urinary incontinence;The evaluation dimensions of model performance include overall performance, discrimination, calibration, and clinical practicability.;Urinary control recovery time;Patient satisfaction;Pelvic floor muscle function indicators; | — |
Secondary
| Measure | Time frame |
|---|---|
| severity of urinary incontinence;Patient compliance; | — |
Countries
China
Contacts
Public ContactZhang Ji
Fudan University Cancer Hospital
Outcome results
None listed