Feasibility Study of an Intervention Therapeutic Education for Patients Treated With Androgen Deprivation

Institut de Cancérologie de la Loire9 enrolled

Overview

The purpose of the study is to build and assess the feasibility of a therapeutic education program, constructed in collaboration with the urologists of the University Hospital of Saint Etienne. The aim of this therapeutic education program is to delay the onset or to reduce the amplitude of the development of insulin resistance and side effects of androgen deprivation therapy in patients treated with androgen deprivation in the context of an evolutive prostate cancer.

Study Type

INTERVENTIONAL

Allocation

Purpose

SUPPORTIVE_CARE

Masking

NONE

Enrollment

Conditions

Prostate Cancer

Interventions

therapeutic education programBEHAVIORAL

Eligibility

Sex: MALEMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Patients supported in consultation Urology at the University Hospital North Saint Etienne. * Aged over 18 years * Having an evolutive prostate cancer * Patient treated with LHRH agonist for at least 6 months - Affiliated with the national health insurance system * And having completed the worksheet informed consent to participate in the program. Exclusion Criteria: * Refusal of participation, protected or under guardianship patients. * Patients unable to understand the study or unable to follow the educational sessions. * Patient (s) with documented cognitive or psychiatric history. * Geographical remotness (more than 100 Kms.)

Locations (2)

CHU Saint-Etienne

Saint-Etienne, France

Institut de Cancérologie de la Loire

Saint-Priest-en-Jarez, France

Outcomes

Primary Outcomes

Number of patients who refused to participate

Time frame: 6 months

Secondary Outcomes

Number of patients in all sessions

Time frame: 6 months

Number of withdrawals

Time frame: 6 months

Data from ClinicalTrials.gov

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