Actively Recruiting

Age: 18Years +
FEMALE
NCT02549157

Treatments for Urogynaecological Problems and Patient Selfreports

Led by Swansea University · Updated on 2024-11-29

500

Participants Needed

1

Research Sites

526 weeks

Total Duration

On this page

Sponsors

S

Swansea University

Lead Sponsor

A

Abertawe Bro Morgannwg University Health Board

Collaborating Sponsor

AI-Summary

What this Trial Is About

The research aims to assess the relationship between treatments for a range of urogynaecological problems (pelvic floor dysfunction, cancers) and patient reported values, psychological states, and quality of life. The impact of treatments on patients' health outcomes will be measured, using specific urogynaecological outcome measures (for either pelvic floor dysfunction or cancer), and patient reported measures of general health and quality of life. Patients' psychological states and values will be measured by validated self-report instruments for these areas. Researchers will obtain consent for participation from patients. Following consent, baseline measures will be taken at the patients' routine appointment about 4 weeks prior to undergoing treatment (e.g., surgery or physiotherapy for pelvic floor dysfunction, or surgery for a urogynaecology cancer). These measures will be the routinely collected physical data obtained by medical staff, and patient reported measures of their general health, psychological state, and quality of life. These questionnaires should take about 30 minutes to complete, in total. The patients will undergo treatment (physiotherapy programme or surgery), which will not be affected by this research. About four weeks post treatment, patients will receive their usual appointment, and routinely collected physical data will be obtained by medical staff, and patients will complete the measures as described above. With the patient's consent, the above evaluation will be repeated at every follow-up appointment that the patient has (i.e. after 3months, and then at yearly intervals, for 5 years). The impact of treatments on objective routine health measures taken by medical staff, and on patient reported measures of health, quality of life, personal values, and psychological functioning, will be documented at each measurement point. Additionally, relationships between psychological states/values and both objective and subjective ratings of how treatments have impacted the patients will be established.

CONDITIONS

Official Title

Treatments for Urogynaecological Problems and Patient Selfreports

Who Can Participate

Age: 18Years +
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Consenting patients who are referred for pelvic floor problems to Singleton Hospital Swansea, UK.
Not Eligible

You will not qualify if you...

  • Under 18 years

AI-Screening

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Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Singleton Hospital

Swansea, United Kingdom, SA2 8PP

Actively Recruiting

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Research Team

L

Lisa A Osborne, D.Phil.

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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