Assessing treatments for urogynaecological issues and patient experiences
Official title: Relationship Between Treatments for Urogynecological Problems and Patient Reported Values, Psychological States, and Quality of Life
Run by Swansea University · NCT02549157 · Data updated 2026-11-12
This study is testing different treatments for urogynaecological issues to see how they affect patients' health and quality of life after treatment.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | Women only |
| Enrollment | 500 (estimated) |
| Sponsor | Swansea University Academic / other |
| Locations | 1 site (Swansea) |
| Status | Recruiting |
| Started | September 1, 2015 |
| Main results expected | September 30, 2025 |
| Study ends | September 30, 2025 |
| Registry record updated | November 29, 2024 |
| Trial ID | NCT02549157 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are consenting patients referred for pelvic floor problems at Singleton Hospital in Swansea, UK.
✕Probably not a fit
Patients under 18 years old will not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This research evaluates the relationship between various treatments for urogynaecological problems, such as pelvic floor dysfunction and cancer, and the resulting patient-reported outcomes, including psychological states and quality of life. Participants will be recruited from Singleton Hospital and will provide baseline measures prior to treatment, followed by assessments at multiple time points post-treatment. The study aims to correlate objective physical outcomes with self-reported health measures and psychological factors to better understand treatment impacts.
Why it matters
Potential benefit: If successful, this study could enhance treatment approaches for urogynaecological conditions by integrating patient-reported outcomes into clinical practice.
How similar studies have gone: While similar studies have explored patient-reported outcomes in urogynaecological treatments, this specific approach of correlating psychological factors with treatment outcomes is relatively novel.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * consenting patients who are referred for pelvic floor problems to Singleton Hospital Swansea, UK. Exclusion Criteria: * under 18 years
Where it's running
-
Singleton Hospital
Swansea, United Kingdom Recruiting
Study contacts
- Principal investigator: Phil Reed, D.Phil. — Swansea University
- Study coordinator: Lisa A Osborne, D.Phil.
- Email: lisa.osborne@nhs.wales.uk
- Phone: 0044 (0)1792 285229
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.