the effectiveness of the continuous care model in patients with bladder cancer

Not Applicable

Recruiting

• Conditions: Bladder Cancer.; Carcinoma in situ of bladder; D09.0

• Registration Number: IRCT20240221061076N1
• Lead Sponsor: Shahid Beheshti University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 6 March 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 58

Inclusion Criteria

The patients include both men and women and are over 18 years of age.
Patients have not performed two or more surgeries at the same time.
Patients have sexual partners.

Exclusion Criteria

Failure to complete the care period
Patients with previous sexual disorders based on the diagnosis of the attending physician
Deterioration of the patient's condition, death of the patient, lack of access of the researcher to the samples, or any condition that makes it impossible for the samples to participate in the research.

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Quality of Life. Timepoint: At the beginning of the study (before the start of the intervention), two weeks after surgery, three months after the intervention. Method of measurement: Aaronson quality of life questionnaire for cancer patients.;Sexual satisfaction. Timepoint: At the beginning of the study (before the start of the intervention), two weeks after surgery, three months after the intervention. Method of measurement: Larson sexual satisfaction questionnaire.;Male sexual function. Timepoint: At the beginning of the study (before the start of the intervention), two weeks after surgery, three months after the intervention. Method of measurement: Questionnaire of the International Index of Erectile Function.;Women's sexual performance. Timepoint: At the beginning of the study (before the start of the intervention), two weeks after surgery, three months after the intervention. Method of measurement: Rozen Women's Sexual Performance Questionnaire.