Prostate Cancer
Conditions
Brief summary
The aim is to built a Therapeutic Education Program for patients treated with radical prostatectomy in order to improve their sexuality. This study is carried out in two steps : * Identification of specific educational objectives through a sociological study, with interviews and focus groups conducted and analyzed by a sociologist. Patients from the urology department of the hospital center (CH) Lyon Sud - Hospices Civils de Lyon (HCL) will be included * Development of the program by a caregiver education expert (Centre Hygée), adapted partly from results of the qualitative study and partly from concepts and tools from the Education Sciences.
Detailed description
8 patients and 2 urologists will be interview to explore the educational needs and to create, expand and validate an interview guide. Exploratory interviews with urologists will address information given to patients on post radical prostatectomy sexual dysfunction, prescribing practices, monitoring therapy (PDE5 inhibitors, IIC, Vacuum), and patients adverse effects management. Focus groups will be conduct to : * Identify the representations associated with erectile dysfunction * Identify the representations related to treatments for erectile dysfunction. * Score patient knowledge about treatments and their managements. * Identify common or original strategies to improve adherence, reduce side effects and overcome the disadvantages of the treatments. * Assessing the needs and expectations of patients
Interventions
Sponsors
Hospices Civils de Lyon
Institut de Cancérologie de la Loire
Study design
Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE
Eligibility
Sex/Gender
MALE
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Patients followed in urology department Lyon Sud CH: * Aged over 18 year * Having a prostate cancer * Treated with radical prostatectomy with or without conservation strips neuro vascular * More than 1 month postoperative * Having a normal preoperative erectile function defined by a score IIEF EF ≥ 26. * And who signed the informed consent form for participation in the study
Exclusion criteria
* Score preoperative IIEF EF \<26 * Refusal of participation, signed consent major patients protected under guardianship. * Patients unable to understand the course of the study * Patient (s) with a documented history of cognitive or psychiatric disorders. * Geographical remoteness of more than 100 Kms.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Thematic and comparative analysis of the recorded interviews | 2 hours | Thematic and comparative analysis of the recorded interviews and transcribed favoring a thematic approach that linked the different elements of speech. |
Countries
France
Outcome results
None listed