Actively Recruiting

Phase Not Applicable
Age: 18Years - 85Years
MALE
NCT06740071

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

Age: 18Years - 85Years
MALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Male patients aged 18 to 85 years
  • Diagnosed with prostate cancer
  • Have undergone laparoscopic radical prostatectomy
Not Eligible

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

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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

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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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