Central Sensitization Inventory and Symptoms of Pelvic Floor Dysfunctions (NCT07154576) | Clinical Trial Compass
By InvitationNot Applicable
Central Sensitization Inventory and Symptoms of Pelvic Floor Dysfunctions
Poland359 participantsStarted 2025-10-28
Plain-language summary
The goal of this observational study is to assess the values of Central Sensitization Inventory in women in a gynecology outpatient clinic. The main question it aims to answer is:
Is there a relationship between outcomes of Central Sensitization Inventory and symptoms of pelvic floor dysfunctions reported by the patients?
Participants will complete questionnaires: Central Sensitization Inventory and questionnaires assessing pelvic floor dysfunctions and their impact on quality of life (PFDI-20, PFIQ-7, PISQ-12).
Who can participate
Age range
18 Years – 80 Years
Sex
FEMALE
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* women attending gynecological outpatient clinics
* Agreement to participate
* Good command of spoken and written Polish
Exclusion Criteria:
* age below 18
* women who have undergone surgical treatment of pelvic organ prolapse or urinary incontinence
* Lack of consent to participate in the study
* Lack of good command of spoken and written Polish
* pregnancy
* women up to 6 months postpartum
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Central Sensitization Inventory (CSI)
Timeframe: baseline measurement
2
Polish version of the Pelvic Floor Distress Inventory (PFDI-20)
Timeframe: baseline measurement
3
Pelvic Organ Prolapse Quantification (POP-Q) system
Timeframe: baseline measurement
4
Polish version of the Pelvic Floor Impact Questionnaire short form 7 (PFIQ-7)
Timeframe: baseline measurement
5
Polish version of the Pelvic Organ Prolapse/Urinary Incontinence Sexual Questionnaire (PISQ-12)