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Application of patient-reported outcomes in rehabilitation of patients with bladder cancer after radical

Study and Application of PRO-Based Symptom Monitoring and Early Warning in the Rehabilitation of Patients After Radical Cystectomy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600118913
Enrollment
Unknown
Registered
2026-02-12
Start date
2023-10-07
Completion date
Unknown
Last updated
2026-02-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bladder tumor

Interventions

Intervention Group:MDASI symptom scale + target symptom monitoring + WeChat - self-assessment twice weekly + alert nurse via WeChat when symptom score exceeds preset threshold + healthcare provider co
Control Group:Routine care model + patient self-referral + no alerts, no feedback

Sponsors

The First Affiliated Hospital of Chongqing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Bladder cancer patients given radical cystectomy+bilateral pelvic lymph node dissection+Bricker urinary diversion; 2.Age >=18 years old; 3.Be able to use WeChat to complete the self-reported scale independently or under the care of a family member; 4.Good physical condition, ECOG score 0 or 1; 5.The patient voluntarily participates and signs an informed consent form;

Exclusion criteria

Exclusion criteria: 1.Serious, uncontrolled comorbidities that may affect protocol adherence or interfere with interpretation of results, These include active opportunistic or progressive (severe) infections, uncontrolled diabetes, cardiovascular disease (heart failure as defined by the New York Heart Association scale as grade III or IV, heart block above grade II, myocardial infarction within the last 6 months, unstable arrhythmia or unstable angina, cerebral infarction within the last 3 months, etc.), or pulmonary disease (interstitial pneumonia, History of obstructive pulmonary disease and symptomatic bronchospasm); 2.Surgery with other large organs was performed within 4 weeks before the start of the program .(Diagnostic surgery is not included);Have a history of psychotropic substance abuse and cannot abstain or have a history of mental disorders;A large amount of pleural fluid or ascites with clinical symptoms or requiring symptomatic management;

Design outcomes

Primary

MeasureTime frame
Quality of Life (QOL);Incidence of Severe Complications;Number of Emergency Department Visits;

Countries

China

Contacts

Public ContactKuang Youlin

The First Affiliated Hospital of Chongqing Medical University

kyl361@163.com+86 23 89011876

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 19, 2026