Prostate Cancer, Prostate Cancer Surgery, Radical Prostatectomies, Rehabilitation Exercise, Rehabilitation Outcome
Conditions
Keywords
radical prostatectomy, rehabilitation, continence, quality of life
Brief summary
In France, a considerable number of radical prostactectomy for cancer is carried out every year.This number was estimated at 20.000 in 2016.This surgery may have negative impact on the continence's subjects and their quality of life. The rehabilitation, preoperative or postoperative, practiced by a physiotherapist, can reduced those side effects. The rehabilitation techniques are many and their efficacy may differ. No study where found about the clasification and evaluation of those rehabilitation techniques.
Detailed description
Investigator aim to create homogeneous clusters of subjects according to the rehabilitation techniques they have received during the preoperative or postoperative period, using a survey replied 6 months after the surgery. To achieve that goal, invesgator will call subjects conduct two interviews. The first interview will take place around one month after the radical prostatectomy and the second around 6 month after the surgery. During those interviews, investigator will question subjects about the rehabilitation techniques practiced on them, about their continence and quality of life. To evaluate the continence investigator will use the survey ICIQ-SF. To evaluate the quality of life, investagator will use the survey KHQ-HR Qol.
Interventions
OTHERQuality of life questionnary
Subjects will be call 1 month and 6 months after prostetectomy to evaluate the type of reeducation received and they will be evaluated with the help of QoL questionnaries : KHQ-HR QoL and ICIQ-SF QoL
Sponsors
Centre Hospitalier de Roubaix
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
MALE
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* men who has undergone a radical prostactectomy to treat a prostatic adenocarcinoma * having a follow up postoperative consultation between one and two month after the surgery * being able to answer to respond the questions during the interviews * agreeing to participate by signing informed consent form
Exclusion criteria
* undergoing an adjuvant therapy as radiotherpy, chemotherapy and hormone therapy * Refusing to take part in the study
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Set up homogeneous groups of subjects (clusters) | It will take place around six months after the surgery. | The primary outcome is a survey questionning the subject about the rehabilitation techniques realised during the post operative period. This survey will be asked during a phone interview directed by investgator. |
Contacts
Primary ContactCamille Trouillet, Clinical Research Associate
Backup ContactMaxence Mokeddem, Clinical Research Assistant
Outcome results
None listed