Intelligent system for diagnosing and treating pelvic floor issues in older women
The Development and Application of an Intelligent Diagnosis and Treatment System for Pelvic Floor Dysfunction in Elderly Women
This study is testing a smart system that helps older women with pelvic floor problems by creating personalized treatment plans to see if they work better than regular exercises.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 300 (estimated) |
| Ages | 60 Years and up |
| Sex | Female |
| Sponsor | Beijing Hospital Government |
| Locations | 1 site (Beijing, Beijing) |
| Trial ID | NCT06372340 on ClinicalTrials.gov |
What this trial studies
This study aims to develop an intelligent diagnosis and treatment system specifically for pelvic floor dysfunction in elderly women. It will assess how to identify variations in pelvic floor muscle function among older women and create personalized treatment plans based on these differences. Participants will receive tailored rehabilitation programs generated by the system, and their treatment outcomes will be compared to those receiving standard pelvic floor muscle training. All examinations and treatments involved are non-invasive.
Who should consider this trial
Good fit: Ideal candidates for this study are women over the age of 60 experiencing pelvic floor dysfunction.
Not a fit: Patients with severe pelvic organ prolapse, a history of pelvic floor surgery, or cognitive impairments may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could lead to more effective and personalized treatments for pelvic floor dysfunction in elderly women.
How similar studies have performed: While the specific intelligent system approach may be novel, similar studies have shown promise in personalized treatment strategies for pelvic floor dysfunction.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: - Women over 60 years old. Exclusion Criteria: * Severe pelvic organ prolapse (POP-Q stage\>III) * History of pelvic floor surgery * Malignant tumor in pelvic * Allergic to nickel * Acute inflammation of pelvic or genital tract * Subjects who has cognitive impairment and cannot sign an informed consent
Where this trial is running
Beijing, Beijing
- Beijing Hospital — Beijing, Beijing, China (Recruiting)
Study contacts
- Study coordinator: Min Li, Ph.D.
- Email: mindy99999@126.com
- Phone: +8613811526308
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.