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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

Observational Overactive Bladder (OAB) Overactive Bladder Syndrome

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Overactive Bladder (OAB), Overactive Bladder Syndrome. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

REVEAL-OAB. 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

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.

Detailed 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.

Primary outcome measures

  • Sexual matters [Time frame: Past four weeks]
  • OAB symptom severity and frequency [Time frame: Past four weeks]
  • Quality of Life relating to bladder symptoms [Time frame: Past four weeks]

Eligibility criteria

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

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Case-only

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT07545148 · 100983

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗