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Correlation Between Quadratus Lumborum , Pelvic Floor Muscles and Diaphragm in Patients With Urinary Incontinence

Sponsor
Deraya University (Other)
Overall Status
Completed
CT.gov ID
NCT05803486
Collaborator
Omar Mohamed Mabrouk (Other), nehad mohamed reda (Other), mohamed ahmed (Other), mohamed ashraf (Other), doaa abdelnaseer (Other)
50
Enrollment
1
Location
2.6
Actual Duration (Months)
19.5
Patients Per Site Per Month

Study Details

Study Description

Brief Summary

The purpose of this study is to investigate Correlation between quadratus lumborum , pelvic floor muscles and diaphragm in patients with urinary incontinence

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    50 patients were distributed randomly into two groups. The first group measured ultrasound imaging for quadratus lumborum , pelvic floor muscles and diaphragm urinary incontinence female The second group measured ultrasound imaging for quadratus lumborum , pelvic floor muscles and diaphragm urinary incontinence female normal females.

    Patients examined with medical ultrasound imaging .

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    50 participants
    Observational Model:
    Other
    Time Perspective:
    Other
    Official Title:
    Correlation Between Quadratus Lumborum , Pelvic Floor Muscles and Diaphragm in Patients With Urinary Incontinence
    Actual Study Start Date :
    Jan 1, 2023
    Actual Primary Completion Date :
    Mar 20, 2023
    Actual Study Completion Date :
    Mar 20, 2023

    Arms and Interventions

    Arm Intervention/Treatment
    experimental group

    examined by ultrasound image to measure quadratus lumborum thickness, pelvic floor muscles force and diaphragm excursion in patients with urinary incontinence
    control group

    examined by ultrasound image to measure quadratus lumborum thickness, pelvic floor muscles force and diaphragm excursion in patients with urinary incontinence

    Outcome Measures

    Primary Outcome Measures

    1. Force of contraction of pelvic floor muscles [2 months]

      by ultrasound imaging, convex transducer was used at a frequency of 5 MHz for evaluating. Voluntary PFM contractions' force (strength) of all patients.

    Secondary Outcome Measures

    1. diaphragm excursion [2 months]

      by ultrasound imaging, convex transducer was used at a frequency of 5 MHz for evaluating. Voluntary diaphragm excursion

    Other Outcome Measures

    1. quadratus lumborum thickness [2 months]

      by ultrasound imaging, convex transducer was use quadratus lumborum thickness

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    30 Years to 40 Years
    Sexes Eligible for Study:
    Female
    Inclusion Criteria:
      • Their ages varied from 30to 40years, their body mass index (BMI) was 25-30 kg/m2 and a number of parities ≤ three normal vaginal deliveries, at least two years and Subjects hadn't received drugs , urinary incontinence mild or modrate
    Exclusion Criteria:
      1. History of spinal surgery or spinal fracture. 2. Volunteers with a history of a recto-vaginal or vesico-vaginal fistula, undiagnosed uterine bleeding urinary tract infection, diabetes, intrauterine device, chest and/or cardiac disease and using any drugs for urinary incontinence 3. Serious diseases, such as heart disease, kidney, liver diseases, gastric ulcer or duodenal ulcer.
    1. A history of bronchial asthma or any chest disease. 5. Uncontrolled diabetes or hypertension. 6. Patients with peacemaker or any metal implant on the treated area. 7. Cancer or patient with past history of tumor excision.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Deraya university Minya Egypt

    Sponsors and Collaborators

    • Deraya University
    • Omar Mohamed Mabrouk
    • nehad mohamed reda
    • mohamed ahmed
    • mohamed ashraf
    • doaa abdelnaseer

    Investigators

    • Principal Investigator: doaa A.Nasser abdelhady, Deraya University

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Deraya University
    ClinicalTrials.gov Identifier:
    NCT05803486
    Other Study ID Numbers:
    • 2\2023
    First Posted:
    Apr 7, 2023
    Last Update Posted:
    Apr 7, 2023
    Last Verified:
    Jan 1, 2023
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:
    Urinary Incontinence
    Enuresis

    Study Results

    No Results Posted as of Apr 7, 2023