- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05567900
Health Care Seeking Behavior and Knowledge Assessment of Hungarian Women About Pelvic Floor Disorders
January 18, 2025 updated by: University of Pecs
Hungarian Women's Health Care Seeking Behavior and Knowledge of Urinary Incontinence and Pelvic Organ Prolapse
The aim of this study is to assess women's health care seeking behavior and knowledge of urinary incontinence and pelvic organ prolapse and to culturally adapt the Prolapse and Incontinence Knowledge Questionnaire (PIKQ) for the Hungarian population.
Study Overview
Status
Completed
Study Type
Observational
Enrollment (Actual)
596
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
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Baranya
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Pécs, Baranya, Hungary, 7621
- University of Pécs
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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
14 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Sampling Method
Non-Probability Sample
Study Population
Women aged 18 years or older who are able to read and write Hungarian.
Description
Inclusion Criteria:
- Woman
- Age 18 and above
- Ability to read and write Hungarian
- Willing to complete the online survey
- Providing consent to participate
Exclusion Criteria:
- Respondents who had already completed the questionnaire on a prior occasion
- Respondents who unable to complete the online survey due to illiteracy
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
- Observational Models: Ecologic or Community
- Time Perspectives: Cross-Sectional
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Urinary incontinence and pelvic organ prolapse knowledge
Time Frame: Baseline
|
The Prolapse and Incontinence Knowledge Questionnaire (PIKQ) is used to assess knowledge.
It consists of two distinct scales: the first one measures knowledge about urinary incontinence knowledge, while the second one measures knowledge about pelvic organ prolapse.
The total score of each scale can range from 0 to 12. Higher scores indicate greater knowledge.
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Baseline
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Health seeking behavior
Time Frame: Baseline
|
Participants report whether they have sought health care for urinary incontinence.
The outcome is the proportion of participants who have ever sought care, among those who reported a history of urinary incontinence.
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Baseline
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Urinary incontinence
Time Frame: Baseline
|
The International Consultation of Incontinence Questionnaire - Short Form (ICIQ-SF) was used to gather information about the symptoms of urinary incontinence.
It contains six questions.
The total score can range from 0 to 21.
Higher scores indicate more severe symptoms.
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Baseline
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Practice of pelvic floor muscle training (PFMT)
Time Frame: Baseline
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The PFMT practice scale of the Pelvic Floor Muscle Training Patient reported Outcome Measures (PFMT-P) was used to assess women's practice of PFMT.
Questions dealt with source of knowledge about PFMT, practice and correct performance.
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Baseline
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Director: Márta Hock, Habilitation, University of Pécs
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)
March 4, 2022
Primary Completion (Actual)
August 26, 2022
Study Completion (Actual)
August 26, 2022
Study Registration Dates
First Submitted
October 3, 2022
First Submitted That Met QC Criteria
October 3, 2022
First Posted (Actual)
October 5, 2022
Study Record Updates
Last Update Posted (Actual)
March 25, 2025
Last Update Submitted That Met QC Criteria
January 18, 2025
Last Verified
January 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Urogenital Diseases
- Mental Disorders
- Male Urogenital Diseases
- Pathological Conditions, Anatomical
- Urologic Diseases
- Female Urogenital Diseases
- Female Urogenital Diseases and Pregnancy Complications
- Urination Disorders
- Lower Urinary Tract Symptoms
- Urological Manifestations
- Behavioral Symptoms
- Elimination Disorders
- Urinary Incontinence
- Enuresis
- Prolapse
- Pelvic Organ Prolapse
Other Study ID Numbers
- BMEÜ/379-3/2022/EKU-1
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
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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