Description Module

Description Module

The Description Module contains narrative descriptions of the clinical trial, including a brief summary and detailed description. These descriptions provide important information about the study's purpose, methodology, and key details in language accessible to both researchers and the general public.

Description Module path is as follows:

Study -> Protocol Section -> Description Module

Description Module


Ignite Creation Date: 2025-12-24 @ 5:10 PM
Ignite Modification Date: 2025-12-24 @ 5:10 PM
NCT ID: NCT05056350
Brief Summary: The diagnosis of breast cancer and the treatments implemented have a significant impact on the professional situation. Maintaining employment and/or reintegration into working life are therefore major issues for cancer patients. This trial proposes to study the feasibility of a support/coaching program for a return to work in patients after breast cancer.
Detailed Description: This study involves patients with breast cancer at the end of their adjuvant treatment. The aim of this study is to evaluate the feasibility of a support program for an adapted return to work of these patients. This back-to-work support program including an individual interview to identify patient needs and expectations, 7 coaching workshops (every 3 weeks +/- 15 days) and a final individual assessment post workshops. The evolution of quality of life, psychological distress and perceptions concerning work will also be evaluated through assessments and questionnaires before (inclusion) and after the support program \[1 month (+/- 7 days) and 6 months (+/- 1 month) after the final individual assessment\]. The study also aims to estimate the recruitment rate in the study and to assess the satisfaction of this support program. Finally, the impact of this support program on the return to work will be described. This initial study will eventually lead to a larger research protocol on the effectiveness of the program, using a randomized controlled trial design.
Study: NCT05056350
Study Brief:
Protocol Section: NCT05056350