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Not yet recruiting NCT07545148

Real-world Experiences and Voices Exploring the Actual Lived Burden of OAB: A Mixed-methods Multi-country PROMs Study on OAB Patients' Quality of Life

Conditions: Overactive Bladder (OAB) Overactive Bladder Syndrome

Sponsor: European Association of Urology Research Foundation

trial.available_in: БГ
Overview
The main goal is to understand what it is truly like to live with OAB from the patient's perspective, including how it affects: daily activities, emotional wellbeing and mental health, social life and relationships, work and overall quality of life.
Description
The REVEAL-OAB (Real-world Experiences and Voices Exploring the Actual Lived burden of Overactive Bladder) study is a large, international, mixed-methods research program designed to capture both the measurable burden and the lived experience of overactive bladder (OAB).Quantitatively, it uses structured surveys and validated patient-reported outcome measures to assess symptom severity (e.g., urgency, frequency, incontinence), health-related quality of life, healthcare utilization, and treatment patterns across diverse populations. Qualitatively, it incorporates in-depth patient interviews, open-ended survey responses, and narrative data to explore how OAB affects emotional wellbeing, social functioning, relationships, and daily decision-making. By integrating these quantitative metrics with rich qualitative insights, the study aims to provide a comprehensive, patient-centered understanding of OAB, identify unmet needs in care, and inform more effective clinical management and health policy.
Who can participate
Inclusion Criteria: * If they are over 18 years old. * They have been told by a doctor or other healthcare professional that they have symptoms that match OAB, or have been given a diagnosis of OAB. * They live in France, Germany, Italy, the Netherlands, Poland, Spain, Sweden, or the UK. * They have received the Patient Information Sheet from their health care provider, during an appointment, via email, or postal mail. * They can confirm they understand the Patient Information Sheet and that they want to take part in this study. Exclusion Criteria: * They have not received information on this study from their own health care provider * They have a confirmed neurological condition known to affect bladder function (for example: multiple sclerosis, Parkinson's disease, spinal cord injury). * They have undergone major surgery directly involving the bladder, prostate, urethra, or pelvic structures that affect urinary function. * They presently have a urinary tract infection (UTI). * They have or have had cancer in their bladder, kidneys, prostate, or other urinary or reproductive organs
Locations

Location information is not available.

Technical details
Status
Not yet recruiting
Study type
OBSERVATIONAL
Sex
Male and female
Minimum age
18 Years
Healthy volunteers
No
Start date
01.07.2026
Completion date
01.02.2027
Registry ID
NCT07545148
Source
clinicaltrials.gov
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