The Intermediate and Long-term Follow up of Home Based Pelvic Muscle Training
Condition(s) studied
Investigational drug(s) / intervention(s)
Home-based pelvic muscle training devices or traditional PFMT at hospital: Performed home-based pelvic muscle training devices at home or traditional PFMT at hospital
Study summary
When participants present with symptoms of pelvic organ prolapse (POP) and stress urinary incontinence (SUI), the investigators will perform a comprehensive evaluation and initially provide conservative treatment. If conservative treatment fails, invasive treatment will be considered. The investigators will arrange a pelvic muscle training course two to three times a week for a duration of 1.5 months per course. However, participants may complain about the inconvenience of traffic, which may lead to discontinuation of the pelvic training course. Therefore, the investigators propose the development of a home-based pelvic muscle training device and will collaborate with information engineering specialists at Tamkang University to invent the device for home-based pelvic muscle training.
Eligibility
Primary outcome measure(s)
- The satisfication of pelvic muscle training (UDI-6) — up to 2 years
The total score ranges from 0 to 18, with a higher score indicating that the patient experiences a greater degree of urinary distress. - The satisfication of pelvic muscle training (ICIQ-SF) — up to 2 years
The total score ranges from 0 to 21, with a higher score indicating that the patient experiences a greater degree of urinary distress. - The satisfication of pelvic muscle training (IIQ-7) — up to 2 years
The total score ranges from 0 to 21, with a higher score indicating that the patient experiences a greater degree of urinary distress. - The satisfication of pelvic muscle training (POPDI-6) — up to 2 years
POPDI-6 scores range from 0 to 24 and higher scores indicate worse bulging symptoms - The satisfication of pelvic muscle training (PISQ-IR) — up to 2 years
The PISQ-IR is a validated questionnaire in research for assessment of female sexual function. A higher score indicates a greater negative impact on sexual function.
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Taipei Veterans General Hospital | Taipei | Taiwan | Recruiting |
More Taipei Veterans General Hospital, Taiwan trials in Taiwan
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT05778552 on ClinicalTrials.gov ↗ ← All trials in Taiwan