Recruiting NA Stress Urinary Incontinence (SUI)

New treatment option for Stress Urinary Incontinence (SUI)

Official title The Impact of Breathing Training on PPSUI: A Randomized Controlled Trial

ClinicalTrials.gov ID: NCT06623617

What this study is testing

What it's testing
\ \ Clinical Trial\ \ This clinical trial aims to investigate the clinical therapeutic effects of breathing training on postpartum stress urinary incontinence (PPSUI). Participants will: All participants will receive standard postpartum care and recovery guidance, including routine examinations, health counseling, basic postpartum recovery recommendations, and educational information.
  • Which group you join is decided by chance.

A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.

Who can take part

Ages 18 and older, women only

You may be able to join if

  • Age: ≥18years
  • 6 weeks to 6 months postpartum
  • Diagnosed with postpartum stress urinary incontinence (PPSUI) by a pelvic floor rehabilitation specialist

You likely can't join if

  • Diabetes mellitus
  • Body mass index (BMI) \>30 kg/m²
  • Cardiopulmonary or renal dysfunction
  • Neurological disorders
  • Pelvic organ prolapse exceeding stage II
  • History of lumbopelvic surgery
See the full eligibility criteria
Who can join
  • Age: ≥18years
  • 6 weeks to 6 months postpartum
  • Diagnosed with postpartum stress urinary incontinence (PPSUI) by a pelvic floor rehabilitation specialist
What rules you out
  • Diabetes mellitus
  • Body mass index (BMI) \>30 kg/m²
  • Cardiopulmonary or renal dysfunction
  • Neurological disorders
  • Pelvic organ prolapse exceeding stage II
  • History of lumbopelvic surgery
  • Lumbopelvic pain
  • Concurrent treatments that may interfere with study outcomes
  • Professional athletes
  • Current pregnancy Withdrawal Criteria:
  • Failure to complete follow-up assessments
  • Loss of contact with participants Termination Criteria:
  • Immediate discontinuation if participants experience dizziness, chest tightness, palpitations, or dyspnea during training
  • Inability to continue intervention due to health issues (e.g., severe complications)
  • Pregnancy occurring during the intervention period
  • Non-compliance with prescribed breathing exercises
  • Participant-initiated withdrawal from the study

The study team makes the final eligibility decision.

Where it's taking place

  • Guangzhou, Shenzhen, China

Questions & answers

Do participants get paid in this trial?

This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.

Is it free to join, and do I need insurance?

Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.

How long does this study last?

The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.

Who can join this trial?

This study is enrolling female, 18 years and older. The study team makes the final eligibility decision.

Where is this trial taking place?

Study sites include Guangzhou, Shenzhen, China. Enter your location above to see the nearest site and check your eligibility.

Explore other conditions

BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.