Assessing women's attitudes towards self-management of vaginal pessaries for pelvic organ prolapse
The Attitude and Success Rate of Women with Pelvic Organ Prolapse on Self-management of Vaginal Pessary: a Multi-centered Prospective Study
This study is trying to see how women feel about using vaginal pessaries on their own to manage pelvic organ prolapse and what factors might influence their comfort with that choice.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 289 (estimated) |
| Ages | 18 Years to 99 Years |
| Sex | Female |
| Sponsor | Chinese University of Hong Kong Academic / other |
| Locations | 1 site (Hong Kong) |
| Trial ID | NCT06246721 on ClinicalTrials.gov |
What this trial studies
This prospective cohort study evaluates women's attitudes and acceptance of self-management using vaginal pessaries for pelvic organ prolapse (POP). It aims to identify factors influencing their willingness to manage their treatment independently. Participants will complete self-administered questionnaires and validated assessments at various intervals to monitor their symptoms and quality of life. The study seeks to enhance patient satisfaction and reduce healthcare costs associated with traditional management methods.
Who should consider this trial
Good fit: Ideal candidates are women suffering from pelvic organ prolapse who require the use of a vaginal ring pessary for treatment.
Not a fit: Patients who are physically dependent, have limited dexterity, are pregnant, have cognitive deficits, or are under 18 years old may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could empower women to manage their pelvic organ prolapse more effectively, improving their quality of life.
How similar studies have performed: While there is limited research specifically on self-management of vaginal pessaries, similar studies on patient empowerment in managing chronic conditions have shown positive outcomes.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: Patient who suffers from pelvic organ prolapse requiring use of vaginal ring pessary as treatment Exclusion Criteria: 1. Physically dependent in their daily living 2. Limited physical dexterity due to medical conditions, for example: Parkinsonism or stroke 3. Pregnancy 4. Cognitive deficit preventing informed consenting procedure and self management 5. Age lower than 18
Where this trial is running
Hong Kong
- The Chinese University of Hong Kong — Hong Kong, Hong Kong (Recruiting)
Study contacts
- Principal investigator: Shing Chee Symphorosa CHAN — O&g, Pwh
- Study coordinator: Symphorosa Shing Chee Chan, Doctor
- Email: symphorosa@cuhk.edu.hk
- Phone: 85255696250
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.