Spinal Curvature, Mobility, and Low Back Pain Relationship in Women With and Without Urinary Incontinence
Primary Purpose
Urinary Incontinence
Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Spinal Mouse® measurement
Low back pain intensity measurement
Urogenital symptoms measurement
Disability caused by low back pain
Sponsored by
About this trial
This is an interventional diagnostic trial for Urinary Incontinence
Eligibility Criteria
Inclusion Criteria:
- aged between 20 and 65 years,
- diagnosed with stress and mixed urinary incontinence
- healthy women
Exclusion Criteria:
- Women with prior history of injury or surgery related to spine,
- spinal deformity,
- systemic pathology,
- any rheumatologic disease,
- neurologic condition,
- symptomatic pelvic organ prolapse,
- malignancy,
- pregnancy
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Experimental
Arm Label
Women with Urinary incontinence
Women without Urinary incontinence
Arm Description
Outcomes
Primary Outcome Measures
Spinal curve and mobility, as measured by Spinal Mouse® device
Secondary Outcome Measures
Low back pain, as measured by Visual Analog Scale
Disability caused by low back pain, as measured by Oswestry Disability Index
Urogenital symptoms, as measured by Urogenital Distress Inventory-6
Full Information
NCT ID
NCT02731339
First Posted
March 30, 2016
Last Updated
April 7, 2016
Sponsor
Ataturk Training and Research Hospital
1. Study Identification
Unique Protocol Identification Number
NCT02731339
Brief Title
Spinal Curvature, Mobility, and Low Back Pain Relationship in Women With and Without Urinary Incontinence
Study Type
Interventional
2. Study Status
Record Verification Date
April 2016
Overall Recruitment Status
Completed
Study Start Date
March 2015 (undefined)
Primary Completion Date
June 2015 (Actual)
Study Completion Date
June 2015 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Ataturk Training and Research Hospital
4. Oversight
5. Study Description
Brief Summary
The aim of this study was to investigate the relationship among sagittal spinal curvatures, mobility, and low back pain in women with and without urinary incontinence.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Urinary Incontinence
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Non-Randomized
Enrollment
73 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Women with Urinary incontinence
Arm Type
Experimental
Arm Title
Women without Urinary incontinence
Arm Type
Experimental
Intervention Type
Device
Intervention Name(s)
Spinal Mouse® measurement
Intervention Description
The sagittal thoracic spinal curvature and mobility of all participants were assessed with Spinal Mouse® (Idiag, Fehraltorf, Switzerland) in standing position.
Intervention Type
Behavioral
Intervention Name(s)
Low back pain intensity measurement
Intervention Description
Low back pain intensity of the patients was questioned by Visual Analogue Scale
Intervention Type
Behavioral
Intervention Name(s)
Urogenital symptoms measurement
Intervention Description
The presence and severity of various urogenital symptoms was assessed with the Urogenital Distress Inventory-6
Intervention Type
Behavioral
Intervention Name(s)
Disability caused by low back pain
Intervention Description
Disability caused by low back pain was assessed with the Oswestry Disability Index
Primary Outcome Measure Information:
Title
Spinal curve and mobility, as measured by Spinal Mouse® device
Time Frame
spinal curve and mobility will be followed through study completion, an average of 3 months
Secondary Outcome Measure Information:
Title
Low back pain, as measured by Visual Analog Scale
Time Frame
Low back pain will be followed through study completion, an average of 3 months
Title
Disability caused by low back pain, as measured by Oswestry Disability Index
Time Frame
Disability will be followed through study completion, an average of 3 months
Title
Urogenital symptoms, as measured by Urogenital Distress Inventory-6
Time Frame
Urogenital symptoms will be followed through study completion, an average of 3 months
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
aged between 20 and 65 years,
diagnosed with stress and mixed urinary incontinence
healthy women
Exclusion Criteria:
Women with prior history of injury or surgery related to spine,
spinal deformity,
systemic pathology,
any rheumatologic disease,
neurologic condition,
symptomatic pelvic organ prolapse,
malignancy,
pregnancy
12. IPD Sharing Statement
Learn more about this trial
Spinal Curvature, Mobility, and Low Back Pain Relationship in Women With and Without Urinary Incontinence
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