This is a single-center, non-randomized feasibility study. For this study, 19 young adults treated for cancer at the Paoli-Calmettes Institute will be included.This study includes interviews and questionnaires to assess the adherence rate. It will be measured by the percentage of patients who attend the first two coaching sessions (either in person or via videoconference) relative to the total number of patients included in the study.
The invitation to participate in this program will be made by the surgeon, hematologist, oncologist, or radiation therapist.
Male or female aged 18 to 25 at the time of cancer diagnosis and/or at the time of inclusion.
In complete remission, within one year following the end of treatment and at the time of inclusion.
Treated at the Comprehensive Cancer Center Institut Paoli-Calmettes.
Able to speak and write in French.
None
Male or female aged 18 to 25 at the time of cancer diagnosis and/or at the time of inclusion.In complete remission, within one year following the end of treatment and at the time of inclusion
Other
Prospective
Not listed
The primary objective of the study is to assess the feasibility of a sport-inspired onco-coaching program by evaluating the participation rate of young adults in the first two coaching sessions.
The primary evaluation criterion of the study will be the adherence rate to the onco-coaching program. It will be measured by the percentage of patients who attend the first two coaching sessions (either in person or via videoconference) relative to the total number of patients enrolled in the study. The invitation to participate in the program will be made by the surgeon, hematologist, oncologist, or radiation therapist.
To identify the success and failure factors of the extrahospital support program through qualitative interviews.
Assessment of participants' satisfaction with the program through semi-structured interviews
To evaluate overall adherence to the onco-coaching program
Compliance with the onco-coaching program, measured empirically across all scheduled visits by assigning equal weight to all participants, regardless of the number of visits planned.
To collect and characterize the reasons why patients decline to participate in the study
Number of refusals to sign the informed consent form.
Click on the lead sponsor to view all of their trials.
