Cancer and Sexual Health : Early Information and Sexual Satisfaction of Couples in Oncology
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Cancer
- Sponsor
- Fondation Hôpital Saint-Joseph
- Enrollment
- 60
- Locations
- 2
- Primary Endpoint
- Change from baseline in Quality Life (QLQ C30) due to a specific information about the sexuality on the sexual satisfaction of the couples, assessed
- Status
- Terminated
- Last Updated
- 8 years ago
Overview
Brief Summary
In a perspective of improvement of the global care of the patients, investigators wish to estimate, within the oncology department of Paris Saint Joseph Hospital, the impact of a clear, written and oral information, on the sexual satisfaction of the couples during treatments.
Further to this study, the project will be to train and to sensitize the medical staff, or still to develop new activities to meet the needs better of patients and of partners.
Detailed Description
To answer the objective, investigators set up a longitudinal study of a maximum duration of 18 months to recruit a minimum of 60 couples distributed in two groups: The inclusion in the study will be made in two phases: * The couples of the non-interventional group (NI) will be recruited at first to avoid the possibility to of sharing information between patients on their care. Indeed, it is about a comparative study and it is necessary that the couples of the NI group do not know about information proposed to the group I, at the risk of cancelling the effect of the information. * The couples of the interventional group (I) will so be recruited during the last phase of the study of the NI group, that is approximately 6 months after the beginning of the study. The choice of the minimal size of participants' sample is stretched out by the necessity of a minimum number of 30 participants by group to make relevant statistical analyses. Once the information were given to the patients and to the partners, according to the group in which they are included, the participants will perform individually same sets of validated questionnaires at three different point times: * initial visit: at the inclusion * intermediate visit: 2 months after the inclusion * final visit: 6 months after the inclusion The Questionnaires will be manage through a local statistical analysis. The set of analyses will be led thanks to the statistical software SPSS. Descriptive analyses of the data, the correlations between the variables of the study and finally the tests of comparison will be perform to have an objective assessment criterion for this study.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Patients and partners declaring itself in couple or having a shared private life;
- •Patients diagnosed by an initial cancer, the prognosis for survival of which at the time of the diagnosis is upper to one year;
- •Patients and partners of more than 18 years old, mastering the French language, and in measure to give their informed consent
Exclusion Criteria
- •Patients having been diagnosed and/or treated for another cancer;
- •Patients and partners having a psychiatric disorder (confusional syndrome, psychotic disorders, disrupted reality perception)
- •Patients and partners protected by the law, according to articles L.1121-5 to L.1121-8 of the Public health code.
Outcomes
Primary Outcomes
Change from baseline in Quality Life (QLQ C30) due to a specific information about the sexuality on the sexual satisfaction of the couples, assessed
Time Frame: Participants will be followed during 6 months
3 times points: Randomization (Day 1), 2 months and 6 months post-inclusion
Secondary Outcomes
- Change from baseline in Sexual Satisfaction Score (ESS) due to a specific information about the sexuality on the sexual satisfaction of the couples, assessed(Participants will be followed during 6 months)