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State of Play of Physiotherapy in the Postoperative Management of Prostate Cancer : Prospective, Monocentric, National Survey, Aiming to Explore the Technics of Physiotherapy (PREduKiné)

C

Centre Hospitalier de Roubaix

Status

Not yet enrolling

Conditions

Prostate Cancer Surgery
Radical Prostatectomies
Rehabilitation Outcome
Prostate Cancer
Rehabilitation Exercise

Treatments

Other: Quality of life questionnary

Study type

Observational

Funder types

Other

Identifiers

NCT06815055
2022-010

Details and patient eligibility

About

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.

Full 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.

Enrollment

510 estimated patients

Sex

Male

Ages

18+ years old

Volunteers

No Healthy Volunteers

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

Trial contacts and locations

0

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Central trial contact

Maxence Mokeddem, Clinical Research Assistant; Camille Trouillet, Clinical Research Associate

Data sourced from clinicaltrials.gov

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