Skip to main content
Clinical Trials/NCT02379260
NCT02379260
Completed
Not Applicable

Development of a Therapeutic Education Intervention Improving Sexuality in Patients With Prostate Cancer Treated With Radical Prostatectomy

Institut de Cancérologie de la Loire1 site in 1 country19 target enrollmentMay 2015
ConditionsProstate Cancer

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Prostate Cancer
Sponsor
Institut de Cancérologie de la Loire
Enrollment
19
Locations
1
Primary Endpoint
Thematic and comparative analysis of the recorded interviews
Status
Completed
Last Updated
10 years ago

Overview

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

Registry
clinicaltrials.gov
Start Date
May 2015
End Date
November 2015
Last Updated
10 years ago
Study Type
Interventional
Study Design
Single Group
Sex
Male

Investigators

Sponsor
Institut de Cancérologie de la Loire
Responsible Party
Sponsor

Eligibility Criteria

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 ≥
  • 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.

Outcomes

Primary Outcomes

Thematic and comparative analysis of the recorded interviews

Time Frame: 2 hours

Thematic and comparative analysis of the recorded interviews and transcribed favoring a thematic approach that linked the different elements of speech.

Study Sites (1)

Loading locations...

Similar Trials