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Clinical Trial Summary

Physical activity (PA) has been an integral part of non-drug therapy since the early 2010s. This supportive care is likely to reduce fatigue and improve the quality of life of patients during and after the cancer treatment phase. Physical activity also has a protective effect in terms of tertiary prevention by reducing the risk of recurrence of certain cancers (breast, colon, prostate) by around 40 to 50% and by reducing overall mortality. Adapted physical activity (APA) is offered at the Institut de Cancérologie de l'Ouest (ICO) in Angers, but there are obstacles particularly linked to the geographical distance of the establishment where this activity is offered. The RAPASS project is a prospective study which will be proposed to patients followed at the ICO, living in rural areas and far from Angers. Its main objective is to describe the fatigue and quality of life of patients before, during and after a 13-session home-based APA programme. The data collected will also be used to describe changes in physical condition and level, compliance with the programme, continuation of physical activity beyond the duration of the programme, and satisfaction.


Clinical Trial Description

The oncologist first assesses the patient's need for APA. The patient is then seen by the ICO's APA coach (EAPA) who presents the APA programme. If the patient agrees to participate, the coach assesses the patient's physical capacity in order to adapt the programme to their needs. The programme is then carried out with the departmental sports for all committee 49. The frequency of practice will ideally be one session per week at the patient's home, supervised by a coach from Departmental Committee for Sport for All in 49. A total of 13 sessions will be carried out. The sessions will aim to develop all the components of physical fitness (endurance, strength, balance, flexibility, coordination, etc.). The patient receives a walking logbook to record the number of daily steps taken, an exercise booklet to work independently and a pedometer. In the presence of the coach, the patients perform different exercises and complete different questionnaires. The programme is evaluated by the ICO EAPA 3 months after the 13th and final session. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05981170
Study type Observational
Source Institut Cancerologie de l'Ouest
Contact Loïc FAIVRE
Phone (0)2 41 35 27 00
Email loïc.faivre@ico.unicancer.fr
Status Not yet recruiting
Phase
Start date September 2023
Completion date March 2025

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