Developing a stepped approach to improving sexual function after treatment for gynaecological cancer

Not Applicable

Completed

• Conditions: Cancer; Psycho-sexual difficulties following treatment for gynaecological cancer

• Registration Number: ISRCTN12010952
• Lead Sponsor: niversity College London (UK)

Brief Summary

2019 results in: https://www.ncbi.nlm.nih.gov/pubmed/30798790 (added 27/02/2019)

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2015-06-04
• Study Completion: 2017-06-30
• Last Update Posted: 5 May 2019

Recruitment & Eligibility

• Status: Completed
• Sex: Female
• Target Recruitment: 100

Inclusion Criteria

1. Women aged over 18 (with partners at their choice) treated for any gynaecological malignancy with surgery and/or chemotherapy and/or radiation at UCLH Gynaecological Cancer Centre or University Hospitals Bristol Gynaecological Cancer Centre
2. 3 months minimum post end of treatment
3. Any sexual orientation
4. With sexual function difficulties identified by initial screen (3 clinical questions within clinical interview posed by doctor or nurse)

Exclusion Criteria

1. Poor English
2. Current drug or alcohol abuse
3. Current sexual therapy or psychotherapy

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<br> Primary endpoints – measures of feasibility:<br> 1. Rate of recruitment<br> 2. Consent rate to randomization and treatment<br> 3. Proportion of women stepping up from level 1 to 2, and level 2 to 3<br> 4. Proportion of women dropping out of therapy<br> 5. Number of usable data points from all measures at all time points<br> 6. Proportion of women lost to follow-up on trial measures<br>