Actively Recruiting
The Application of Somatosensory Interactive Pelvic Floor Muscle Training for Stress Urinary Incontinence in Men Underwent Radical Prostatectomy
Led by The University of Hong Kong · Updated on 2025-04-04
100
Participants Needed
2
Research Sites
204 weeks
Total Duration
On this page
Sponsors
T
The University of Hong Kong
Lead Sponsor
R
Ruijin Hospital
Collaborating Sponsor
AI-Summary
What this Trial Is About
The study aims to compare the efficacy of different pelvic floor muscle training (PFMT) modes on improving urinary incontinence (UI) recovery in prostate cancer (PCa) patients after radical prostatectomy (RP). The methods being compared include standard PFMT (S-PFMT) , a somatosensory interactive PFMT (SI-PFMT, an enhanced PFMT) , and a standard PFMT combined with pelvic floor muscle magnetic stimulation (S-PFMT+MS). Eligible participants are randomized into either of the groups to receive different modalities of post-operative PFMT. Subjects in the S-PFMT group received traditional verbal instructions and paper-based educational materials. For the SI-PFMT group, an interactive experiential education model was adopted. First, an educational video introduced the importance and basic information of postoperative PFMT. Then, synchronized PFMT guidance through a combination of audio and video would be used. Subjects assigned to the S-PFMT+MS group, on the basis of traditional verbal and paper-based education, pelvic floor magnetic stimulation therapy was applied using a pelvic floor magnetic stimulator, operated by the same experienced rehabilitation physician. Self administered questionnaires and 1-hour pad test would be used to assess the treatment outcomes at 1, 3, and 6 months postoperatively.
CONDITIONS
Official Title
The Application of Somatosensory Interactive Pelvic Floor Muscle Training for Stress Urinary Incontinence in Men Underwent Radical Prostatectomy
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Male patients aged 18 to 85 years
- Diagnosed with prostate cancer
- Have undergone laparoscopic radical prostatectomy
You will not qualify if you...
- Currently participating in other clinical trials
- Unable to cooperate with study treatments and follow-up procedures due to specific factors
AI-Screening
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Trial Site Locations
Total: 2 locations
1
Ruijin Hospital
Shanghai, Shanghai Municipality, China, 200025
Actively Recruiting
2
Queen Mary Hospital
Hong Kong, Hong Kong, Hong Kong
Actively Recruiting
Research Team
R
Research Assistant, BSc
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
3
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