Actively Recruiting
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
Eligibility Criteria
You may qualify if you...
- Consenting patients who are referred for pelvic floor problems to Singleton Hospital Swansea, UK.
You will not qualify if you...
- Under 18 years
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Trial Site Locations
Total: 1 location
1
Singleton Hospital
Swansea, United Kingdom, SA2 8PP
Actively Recruiting
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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