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State of Play of Physiotherapy in the Postoperative Management of Prostate Cancer (PREduKiné)

Not yet recruiting
Conditions
Radical Prostatectomies
Rehabilitation Outcome
Prostate Cancer
Prostate Cancer Surgery
Rehabilitation Exercise
Registration Number
NCT06815055
Lead Sponsor
Centre Hospitalier de Roubaix
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.

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
Male
Target Recruitment
510
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

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
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.

Secondary Outcome Measures
NameTimeMethod
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