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Clinical Trials/NCT07004738
NCT07004738CompletedNot Applicable

Ultrasound Assessment of Rectus Abdominis Muscle Thickness and Residual Bladder Volume Before and After Pelvic Floor Exercises

Istanbul Medipol University Hospital1 site in 1 country40 target enrollmentStarted: May 26, 2025Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
40
Locations
1
Primary Endpoint
Ultrasound Measurements

Study Overview

Brief Summary

The study will be conducted on 40 women between the ages of 20-40 who volunteer to participate in the study. All participants will be selected from individuals who have been diagnosed with pelvic floor dysfunction and have no history of pelvic surgery. Pelvic floor dysfunction will be diagnosed by an Obstetrics and Gynecology Specialist. Participants will be divided into two groups as the Pelvic floor exercise group and the control group.

Detailed Description

The study will be conducted on 40 women between the ages of 20-40 who volunteer to participate in the study. All participants will be selected from individuals who have been diagnosed with pelvic floor dysfunction and have no history of pelvic surgery. Pelvic floor dysfunction will be diagnosed by an Obstetrics and Gynecology Specialist. Participants will be divided into two groups as the Pelvic floor exercise group and the control group. Group distributions will be made by randomization.org website. Participants in the pelvic floor exercise group will be instructed to do daily pelvic floor exercises under the guidance of a physiotherapist specialized in pelvic health. No exercises will be given to women diagnosed with pelvic floor dysfunction in this group. Women will continue their routine lives and their evaluations will be made.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Participant)

Masking Description

Participants will be masked.

Eligibility Criteria

Ages
20 Years to 40 Years (Adult)
Sex
Female
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •were being between 20-40 years of age,
  • •having pelvic floor dysfunction,
  • •not having any problems that would prevent performing pelvic floor exercises

Exclusion Criteria

  • •previous pelvic surgery
  • •active urinary tract infections
  • •neurological conditions affecting bladder control

Arms & Interventions

Pelvic floor exercise group

Experimental

Participants will be instructed to perform daily pelvic floor exercises under the guidance of a physical therapist specializing in pelvic health. The exercises focus on isolated pelvic muscle contractions and core muscle engagement. The exercises will be performed 3 times per day for 6 weeks.

Intervention: Pelvic floor exercises (Other)

Control Group

Other

Women in this group who have been diagnosed with pelvic floor dysfunction will not be given any exercises. Women will continue their routine lives and their evaluations will be made.

Intervention: Control group (Other)

Outcomes

Primary Outcomes

Ultrasound Measurements

Time Frame: 20 minutes

Ultrasound measurements will be performed at two points: at baseline (before the exercise program) and after 6 weeks of intervention. A high-resolution ultrasound device will be used to measure the thickness and cross-sectional area of the rectus abdominis muscle at rest.

The residual bladder volume measurement

Time Frame: 20 minutes

The residual bladder volume immediately after voiding will also be measured by ultrasonography to assess bladder control.A normal post-void residual volume is between 50 mL (milliliters) and 100 mL.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Istanbul Medipol University Hospital
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

merve yilmaz menek

Principal Investigator

Istanbul Medipol University Hospital

Study Sites (1)

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