← Eichor
Study identifier: NCT07243028 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Ultrasound and Electromyography Biofeedback for Pelvic Floor Muscle Training

Condition: Pelvic Floor Dysfunction · Pelvic Floor Muscle Weakness  ·  Sponsor: National Cheng-Kung University Hospital

PhaseNA
Planned participants70
Who can joinFemale, 21 Years to no upper limit
Healthy volunteersNo

About this study

This study aims to investigate the factors influencing adherence to pelvic floor muscle training (PFMT) devices among patients with pelvic floor dysfunction (PFD) through structured questionnaires, while simultaneously comparing the effectiveness of different feedback modalities, including non-invasive ultrasound imaging and invasive manometry with electromyography (EMG). By integrating subjective adherence data with objective performance outcomes, the project seeks to evaluate the potential of system-level integration for personalized therapeutic strategies, ultimately enhancing treatment efficacy, improving patient satisfaction, and promoting sustained engagement in PFMT.

This description comes directly from the study's public registry record.

Talk to the study team

Li-Chieh Kuo, Ph. D.  ·  886-62353535  ·  jkkuo@mail.ncku.edu.tw

Always discuss trial participation with your own doctor first.

Locations (1)

National Cheng-Kung University HospitalTainan, Taiwan, TaiwanRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT07243028