Implementation of a "Remission" Consultation in the Management of Patients Treated for Localized Breast Cancer
- Conditions
- Breast Neoplasms
- Interventions
- Other: Remission Consultation
- Registration Number
- NCT02740491
- Lead Sponsor
- Centre Hospitalier Universitaire de Nīmes
- Brief Summary
The main objective of this study is to describe the evolution in quality of life (QLQ-C30) for patients receiving breast cancer care at 3, 6 and 12 months after a "remission" consultation.
- Detailed Description
The secondary objectives of this study are:
A. to describe changes in body image (Image Body Scale Version F) at 3, 6 and 12 months after a "remission" consultation.
B. to describe changes in psychological distress (visual analog scale) at 3, 6 and 12 months after a "remission" consultation.
C. to assess the time of resumption of work (date of last chemotherapy - date of the actual resumption of work) after a "remission" consultation.
D. to evaluate the acceptance rate for the "remission" consultation.
E. to describe the modes of the observed management, their distribution and the characteristics of the patients according to different monitoring arrangements.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- Female
- Target Recruitment
- 50
- The patient is receiving care for localized breast cancer and finished her adjuvant treatment (chemotherapy, radiotherapy)
- The patient has completed his/her adjuvant therapy in the last 6 months (chemotherapy, radiotherapy).
- The patient is participating in another study
- The patient is under judicial protection
- It is impossible to correctly inform the patient
- The patient has a metastatic form of the disease at diagnosis
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description The study population Remission Consultation The study population consists of adult patients diagnosed with localized breast cancer who have completed adjuvant treatment (chemotherapy, radiotherapy) and who are cared for in the Medical Oncology department of the Nîmes University Hospital.
- Primary Outcome Measures
Name Time Method The EORTC QLQ-C30 questionnaire Month 12
- Secondary Outcome Measures
Name Time Method Psychological distress (visual analog scale) Month 12 Work recovery time (date of last chemotherapy - date of the actual resumption of work) Month 12 Body Image Scale Month 12 Acceptance of remission consultation (yes/no) Day 0
Trial Locations
- Locations (1)
CHRU de Nîmes - Hôpital Universitaire Carémeau
🇫🇷Nîmes Cedex 09, France