RectSexQol: Study of the Prevalence of Sexual Dysfunction in Women After Rectal Cancer Surgery and Analysis of the Impact of a Sexologist Intervention

Sponsor
University Hospital, Limoges (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05933122
Collaborator
(none)
144
6
2
42.1
24
0.6

Study Details

Study Description

Brief 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.

Condition or Disease Intervention/Treatment Phase
  • Other: sexologist consult
  • Other: standart of care
N/A

Detailed Description

The treatment of rectal cancer is multimodal combining surgery, chemotherapy and radiotherapy. Each therapeutic tool may affect the sexual life of treated patients.

The incidence of sexual dysfunction in patients with rectal cancer varies according to literature from 5 to 88%. This may be due to the lack of a common definition relating to sexual dysfunction making it difficult to compare results. On the other hand, it should be noted that all of the work related to sexual dysfunction after treatment for rectal cancer is mainly interested in men. The sexual well-being of women treated for rectal cancer is based on the assessment and management of their sexual functions as well as that of their overall sexual health in a personalized manner. The establishment of a sexology consultation before and after such a surgical procedure could improve the sexual functions as well as the sexual well-being of these women. The main aim of our study is to evaluate the prevalence of sexual dysfunctions at M-1 (before treatment) in the two cohorts "here" and "elsewhere" in the context of surgery for rectal cancer in females. The second aim will be to determine the impact of sexology consultation in the cohort "here" in comparison to the standart cohort without any intervention called "elsewhere".

Study Design

Study Type:
Interventional
Anticipated Enrollment :
144 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Cohort called "elsewhere" = cohort without specific care by a sexologist Cohort called "here" = cohort with an intervention by a sexologistCohort called "elsewhere" = cohort without specific care by a sexologist Cohort called "here" = cohort with an intervention by a sexologist
Masking:
None (Open Label)
Primary Purpose:
Other
Official Title:
Study of the Prevalence of Sexual Dysfunction in Women After Rectal Cancer Surgery and Analysis of the Impact of a Sexologist Intervention
Anticipated Study Start Date :
Aug 1, 2023
Anticipated Primary Completion Date :
Sep 1, 2026
Anticipated Study Completion Date :
Feb 1, 2027

Arms and Interventions

Arm Intervention/Treatment
Sham Comparator: Cohort called "elsewhere"

cohort without specific care by a sexologist

Other: standart of care
in the cohort called "elsewhere" , patients will be treated according to standards of care, without specific care by a sexologist

Experimental: Cohort called "here"

cohort with an intervention by a sexologist

Other: 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.

Outcome Measures

Primary Outcome Measures

  1. 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

Secondary Outcome Measures

  1. Number and proportion of women with sexual dysfunction defined as a total FSFI score greater than 26.55 at Month 6 and Month 12 after usual or specific management in the context of surgery for rectal cancer [Month 12]

    Number and proportion of women with sexual dysfunction defined as a total FSFI ("Female Sexual Function Index") score greater than 26.55 at Month 6 and Month 12 after usual ("elsewhere" cohort) or specific management (duration of 6 months) ("here" cohort, including consultations by a sexologist supervising the surgical procedure) in the context of surgery for rectal cancer

  2. Change in the score of the "satisfaction" dimension of the FSFI scale between Month -1, Month 6 and Month 12 [Month 12]

    Change in the score of the "satisfaction" dimension of the FSFI scale between Month -1, Month 6 and Month 12

  3. Differences (Month 6 - Month -1 and Month 12 - Month 6) in the score of the "satisfaction" dimension of the FSFI scale (Q14-Q16) between the groups with and without treatment by a sexologist (cohort here vs. elsewhere) [Month 12]

    Differences (Month 6 - Month -1 and Month 12 - Month 6) in the score of the "satisfaction" dimension of the FSFI scale (Q14-Q16) between the groups with and without treatment by a sexologist (cohort here vs. elsewhere)

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Women

  • Diagnosis of stage I-III rectal adenocarcinoma or rectosigmoid junction with anastomosis less than 15 cm from the anal margin

  • Surgical management, preceded or not by Radio-chemotherapy, with restoration of continuity

  • Age : over 18

  • Proficiency in French or English

Exclusion Criteria:
  • Current pregnancy

  • Significant cognitive/psychiatric disorders

  • Guardianship

Contacts and Locations

Locations

Site City State Country Postal Code
1 Brive Hospital Brive-la-Gaillarde France 19100
2 Les cedres Clinical Brive-la-Gaillarde France 19316
3 Gueret Hospital Guéret France 23000
4 Chenieux clinical Limoges France 87039
5 Limoges University Hospital Limoges France 87042
6 Saint Junien Hospital Saint-Junien France 87200

Sponsors and Collaborators

  • University Hospital, Limoges

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University Hospital, Limoges
ClinicalTrials.gov Identifier:
NCT05933122
Other Study ID Numbers:
  • 87RI22_0006
First Posted:
Jul 6, 2023
Last Update Posted:
Jul 6, 2023
Last Verified:
Jun 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by University Hospital, Limoges
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 6, 2023