- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06470620
The Relationship Between Pelvic Floor Muscle Function and Hip Pain Among Women
January 23, 2026 updated by: Gali Dar, University of Haifa
This study examines the relationship between pelvic floor muscle (PFM) function and self-perception of PFM contraction with hip pain, their severity, and hip muscle strength.
In addition, it will examines the association between PFM function, and anxiety.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
This cross-sectional study will include women with symptoms of hip-related pain persisting > three months(research group), and women without hip pain (control group).
A single session will include various assessments as follows: abdominal ultrasound examination to evaluate PFM function and endurance, in addition, each participant will evaluate her ability to perform correct contraction of PFM, hand-held dynamometer testing for hip rotator muscle strength, the International Consultation on Incontinence Questionnaire (ICIQ) for evaluating symptoms and impact of urinary incontinence, the International Hip Outcome Tool 12 for assessing hip function and pain, the Hospital Anxiety & Depression Scale (HADS), and a functional performance task involving the hip muscles - a single-leg squat.
Study Type
Observational
Enrollment (Actual)
51
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Haifa District
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Haifa, Haifa District, Israel, 31905
- Haifa University, Department of PHysical Therapy
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Yes
Sampling Method
Non-Probability Sample
Study Population
women with and without hip related pain
Description
Inclusion Criteria for Research Group:
- complaints of hip related pain,
- Visual Analog Scale (VAS) >3 for three months,
- with one or more of the symptoms relevant to the syndrome - (1) hip or groin pain produced by a certain movement or position, stiffness and limitation of movement or clicks from the hip joint, (2) examination A positive FADIR performed by the researcher before conducting the study
Exclusion criteria:
- the presence of additional diagnoses of the slipped capital femoral epiphysis,
- Perthes disease,
- avascular necrosis, and osteoarthritis-Calve-Legg,
- neurological or Metabolism,
- surgery/fracture in the hip joint of which the woman complains,
- pregnancy or childbirth in the last year,
- Treatment of the pelvic floor in the last year.
control group - health women without any pain or symptoms in the spine and lower extremities
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
research group
women with hip-related pain
|
no intervention will be performed - several diagnostic assessments tools
Other Names:
|
|
control group
healthy women without hip pain
|
no intervention will be performed - several diagnostic assessments tools
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
urinary bladder displacement in millimeters
Time Frame: baseline
|
bladder displacement will be measured via diagnostic ultrasound using the on screen caliper tool
|
baseline
|
|
International Consultation on Incontinence Questionnaire
Time Frame: baseline
|
evaluating the frequency, severity and impact on quality of life of urinary incontinence.
The score ranges from 0-21, with a higher score indicating greater severity
|
baseline
|
|
pelvic floor muscle function assessed as correct movement of the urinary bladder
Time Frame: baseline
|
upward or downward displacement of urinary bladder will be measured via diagnostic ultrasound.
Upward movement is considered the correct direction describing good function of pelvic floor muscles
|
baseline
|
|
pelvic floor muscles endurance of contraction in seconds
Time Frame: baseline
|
The participant is instructed to contract pelvic floor muscle and hold the contraction as long as possible.
bladder status on ultrasound is assessed.
When the bladder starts to move downward from its position the examination ends.
(measured in sec).
|
baseline
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
muscle strength
Time Frame: baseline
|
hip muscle abduction sill be measure via hand held dynamometer
|
baseline
|
|
self-reporting of fear and anxiety of hip pain regarding quality of life
Time Frame: baseline
|
Hospital Anxiety & Depression Scale
|
baseline
|
|
hip range of motion
Time Frame: baseline
|
range of motion will be assessed with goniometer
|
baseline
|
|
function assesment
Time Frame: baseline
|
single leg squat
|
baseline
|
|
hip function assessment
Time Frame: baseline
|
International Hip Outcome Tool 12 questionnaire.
range 0-100, with a high score indicates a high quality of life
|
baseline
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Gali Dar, Prof., University of Haifa
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
September 1, 2024
Primary Completion (Actual)
September 15, 2025
Study Completion (Actual)
September 15, 2025
Study Registration Dates
First Submitted
June 17, 2024
First Submitted That Met QC Criteria
June 17, 2024
First Posted (Actual)
June 24, 2024
Study Record Updates
Last Update Posted (Actual)
January 26, 2026
Last Update Submitted That Met QC Criteria
January 23, 2026
Last Verified
January 1, 2026
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
- Urogenital Diseases
- Male Urogenital Diseases
- Urologic Diseases
- Female Urogenital Diseases
- Female Urogenital Diseases and Pregnancy Complications
- Urination Disorders
- Lower Urinary Tract Symptoms
- Urological Manifestations
- Urinary Incontinence
- Pathological Conditions, Signs and Symptoms
- Signs and Symptoms
- Urinary Incontinence, Stress
Other Study ID Numbers
- 122/24 (St Vincent's Hospital Melbourne Human Research Ethics Committee)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
IPD Plan Description
following study completion, a paper will be submitted to international professional journal
IPD Sharing Time Frame
6 months following end of study
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- CSR
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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