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Complex intervention strategy for older women with urinary incontinence in community: a feasibility study

Complex intervention strategy for older women with urinary incontinence in community: a feasibility study

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300076166
Enrollment
Unknown
Registered
2023-09-26
Start date
2023-10-10
Completion date
Unknown
Last updated
2023-10-03

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

Conditions

urinary incontinence

Interventions

Intervention group:Complex intervention strategy for older women with urinary incontinence in the community, including physical assessment, health education, pelvic floor muscle exercise, reminder sup
Control group:The control group received health education. A seminar on urinary incontinence will be held in the community activity center for older women
a manual on urinary incontinence health education will be produced and distributed
and articles and short videos on urinary incontinence will be pushed through WeChat. The content of health education includes: knowledge about urinary incontinence which including the prevalence of ur
knowledge about pelvic floor muscle exercises which including the methods and benefits of pelvic floor muscle exercises, and the economic costs that may be incurred in the process of exercising.

Sponsors

Xiangya School of Public Health, Central South University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
60 Years to 90 Years

Inclusion criteria

Inclusion criteria: (i) older women aged =60 years and able to walk to the community center; (ii) Suffering from mild or moderate urinary incontinence for more than 3 months (those who scored 1-14 on the International Consultation on Incontinence Questionnaire-short form); and (iii) Study subjects gave informed consent, participated voluntarily, and signed a consent form;

Exclusion criteria

Exclusion criteria: (i) those with terminal disease and expected survival = 12 months; (ii) those with dementia or severe significant cognitive impairment; (iii) those with Parkinson's disease and a history of Parkinson's syndrome, epilepsy, malignancy, etc.; (iv) those with severe functional deficits in vision, hearing, comprehension, etc., that impede the conduct of the study; and (v) those who are participating in other intervention programs.

Design outcomes

Primary

MeasureTime frame
Acceptability of Intervention;Intervention Appropriateness;Feasibility of Intervention;

Secondary

MeasureTime frame
Adverse events;Improvement in urinary incontinence symptoms;Improved quality of life;

Countries

China

Contacts

Public ContactWenqi Liu

Xiangya School of Public health, Central South University

1798143380@qq.com+86 151 7340 2972

Outcome results

None listed

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