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Management of urinary incontinence based on multidisciplinary team decision-making in Chinese older adults(CO-MUI study): a prospective, multicenter, randomized, controlled study

Management of urinary incontinence based on multidisciplinary team decision-making in Chinese older adults(CO-MUI study): a prospective, multicenter, randomized, controlled study

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200056699
Enrollment
Unknown
Registered
2022-02-10
Start date
2022-02-28
Completion date
Unknown
Last updated
2023-09-04

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

Conditions

urinary incontinence

Interventions

experimental group:Implement a multidisciplinary team management strategy integrating non-surgical and surgical treatment according to evidence-based guidelines
control group:Routine treatment management mode

Sponsors

Xuanwu Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Patient age = 60 years old; 2. Clear awareness, normal language expression ability, and able to communicate effectively; 3. Conforming to the diagnosis of urinary incontinence; 4. Estimated hospital stay = 4 days; 5. Can be followed up for more than 1 year; 6. Sign the informed consent form and voluntarily participate in the research.

Exclusion criteria

Exclusion criteria: 1. Mental, conscious and severe cognitive impairment, unable to communicate effectively; 2. The patient has poor compliance and cannot cooperate to complete the assessment and intervention; 3. The patient and his family refused to participate in the study; 4. End stage of disease; Acute myocardial infarction; Dissecting aortic aneurysm; Severe aortic valve stenosis; Endocarditis/acute pericarditis; Acute thromboembolism; Recent major surgery or limb fracture in the past month; 5. There are other conditions that the researcher believes need to be excluded.

Design outcomes

Primary

MeasureTime frame
score of ICI-Q-SF;

Secondary

MeasureTime frame
routine urine test;postvoid residual volume;urodynamics;ADL;CAM;SAS;GDS-15;all-cause death;

Countries

China

Contacts

Public ContactLi Yun

Xuanwu Hospital, Capital Medical University

liy_xw@sina.com+86 13601307723

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026