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Clinical Trials/KCT0003357
KCT0003357Active, not recruiting未知

Effect of neuromuscular electrical stimulation using novel device on pelvic floor muscle and gluteus muscle strength, lumbopelvic stability, bladder neck mobility and sexual function in patients with stress urinary incontinence

Yonsei University0 sites72 target enrollmentStarted: TBDLast updated:

Trial Snapshot

Phase
未知
Status
Active, not recruiting
Enrollment
72

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional Study

Eligibility Criteria

Ages
30(Year) to 60(Year) (—)
Sex
Female

Inclusion Criteria

  • 1) Subjects who were clinically diagnosed with stress incontinence
  • 2) Subjects who experienced leakage of urine during the last 3 months
  • 3) Body mass index Body mass index (BMI) <30 kg / m²
  • 4) Subjects with age between 30 and 60
  • 5) Subjects who are not addicted to drugs or alcohol
  • 6) Subjects who can perform the questionnaire or medical diagnosis successfully

Exclusion Criteria

  • 1) Subjects with Urogenital prolapse grade III or higher
  • 2) Subjects with Pacemaker
  • 3) Subjects who are allergic to electric stimulation or gel pad
  • 4) Subjects with artificial joints in the hip or pelvis
  • 5) Subjects with chronic systemic, neurological and connective tissue diseases
  • 6) Those who are pregnant or have a pregnancy plan
  • 7) Subjects who are extremely sensitive to electrical stimulation and unable to train pelvic floor muscle electrical stimulation
  • 8) Patients who have had surgery on the pelvic or abdomen in the past 6 months
  • 9) Subjects with cognitive impairment
  • 10) Subjects who did not fully participate in pelvic floor muscle electrical stimulation training
  • 11) Subjects with blood disorders or diabetes, hypertension

Investigators

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