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

Institut de Cancérologie de la Loire

Status

Completed

Conditions

Prostate Cancer

Treatments

Behavioral: therapeutic education program

Study type

Interventional

Funder types

Other

Identifiers

NCT02460549

2014-04

2013-A01169-36 (Other Identifier)

Details and patient eligibility

About

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.

Enrollment

9 patients

Sex

Male

Ages

18+ years old

Volunteers

No Healthy Volunteers

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.)