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Clinical Trials/NCT07320573
NCT07320573
Not yet recruiting
Not Applicable

Evaluation of Pelvic Floor Muscle Strength in Women With Stress Urinary Incontinence Using Two Different EMG Methods

Ahi Evran University Education and Research Hospital1 site in 1 country24 target enrollmentStarted: January 2, 2026Last updated:

Overview

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Ahi Evran University Education and Research Hospital
Enrollment
24
Locations
1
Primary Endpoint
pelvic floor muscle strength

Overview

Brief Summary

Pelvic floor muscle strength will be measured in women with stress urinary incontinence using superficial EMG, intravaginal EMG, and digital palpation. A 10-minute rest period will be given between each measurement, and the results will be recorded. Once all measurements are completed, any differences between the three measurements will be examined.

Detailed Description

Pelvic floor muscle strength will be assessed by vaginal palpation in the women included in the study. Then, patients will be placed in a hook position for EMG measurement. For superficial measurement, electrodes will be placed on the levator ani muscle on either side, and then the first assessment will be performed in 3 trials consisting of 5 seconds of contraction followed by 5 seconds of rest, and the second assessment in 3 trials consisting of 2 seconds of contraction followed by 5 seconds of rest.

Measurement with an intervaginal electrode will also be performed in the supine hook position, using a passive electrode and an active vaginal probe. Lubricant gel will be applied to the vaginal probe before insertion into the vagina, and the passive electrode will be placed on the inner surface of the right thigh (adductor muscle group). Two different protocols will be used for assessment. The first assessment will consist of 3 trials of 5 seconds of contraction followed by 5 seconds of rest, and the second assessment will consist of 3 trials of 2 seconds of contraction followed by 5 seconds of rest. A 10-minute rest period will be included between measurements. The ICIQ-SF questionnaire will also be used to determine the type and degree of incontinence. Participants will be asked to answer the questions considering the last two weeks. A score will then be assigned.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to 70 Years (Adult, Older Adult)
Sex
Female
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Being over 18 years of age
  • Having stress urinary incontinence
  • Being willing to participate in the study

Exclusion Criteria

  • Unwillingness to continue working
  • Presence of a neurological disease

Outcomes

Primary Outcomes

pelvic floor muscle strength

Time Frame: day 1

muscle strength and endurance durations

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Ahi Evran University Education and Research Hospital
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Esra BAYRAMOĞLU DEMİRDÖĞEN

LecTURER DOCTOR

Ahi Evran University Education and Research Hospital

Study Sites (1)

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