Study of the Prevalence of Sexual Dysfunction in Women After Rectal Cancer Surgery and Analysis of the Impact of a Sexologist Intervention
Condition(s) studied
Investigational drug(s) / intervention(s)
sexologist consult: in the cohort called "here", after the diagnosis of rectal cancer, patients will be seen by a sexologist before any kind of treatment for rectal cancer. Sexual dysfunctions will be assessed by a sexologist. After the surgery of rectal cancer, the sexologist will see them again to assess sexual dysfunctions after such a management of rectal cancer. If there is any discovery of a sexual dysfunction or aggravation of a previous one or alteration of sexual life, the sexologist will help the patients to improve their sexual quality of life.
standart of care: in the cohort called "elsewhere" , patients will be treated according to standards of care, without specific care by a sexologist
Study summary
RectSexQoL is a study aiming at determining the prevalence of female sexual dysfunction after rectal cancer surgery. It has the goal as well to analyse the impact of an intervention given by a sexologist to such patients.
Eligibility
Primary outcome measure(s)
- Number and proportion of women with sexual dysfunction defined as a total FSFI — Month -1
Number and proportion of women with sexual dysfunction defined as a total FSFI ("Female Sexual Function Index") score greater than 26.55 at Month -1 (before any treatment) in the context of surgery for rectal cancer
Trial sites (6)
| Facility | City | Region | Status |
|---|---|---|---|
| Brive Hospital | Brive-la-Gaillarde | France | Recruiting |
| Les cedres Clinical | Brive-la-Gaillarde | France | Recruiting |
| Gueret Hospital | Guéret | France | Recruiting |
| Chenieux clinical | Limoges | France | Not Yet Recruiting |
| Limoges University Hospital | Limoges | France | Recruiting |
| Saint Junien Hospital | Saint-Junien | France | Recruiting |
More University Hospital, Limoges trials in France
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT05933122 on ClinicalTrials.gov ↗ ← All trials in France