Preparation for Medical and Surgical Procedures in Oncogeriatry.
Condition(s) studied
Investigational drug(s) / intervention(s)
Personalized pre-habilitation program: Each patient will undergo 4 weeks of individualized pre-habilitation before surgery. Each session (1 session per day) will be carried out autonomously by the patient at home, via a dedicated application (Activiti Pro) installed on their tablet or smartphone.
Study summary
Surgical management is one of the most frequently used interventions in the treatment of many cancers, but it can be associated with a high risk of postoperative complications.
The maintenance and optimization of functional abilities before, during and after treatment are major for elderly cancer patients, as it is now well established that there is a link between the level of functional capacity and the occurrence of these complications.
The scientific literature shows that the benefits of pre- and post-operative training programs, but these benefits only apply to a fraction of the patients adhering to the programs. The modalities of intervention (training load, follow-up, etc.) as well as patient involvement in these programs are major issues that need to be addressed to optimize their benefits.
Individualizing pre-habilitation, on the basis of the management of the training load, and therefore objective fatigue, would enable better patient adherence to the program, and optimize its benefits.
In this context, the PRIMECHO project aims to individualize pre-habilitation in order to improve functional of patients in the pre-habilitation or accelerated recovery after surgery phase. The aim is for the patient to be in optimum physical condition at the time of the intervention or treatment.
Eligibility
Primary outcome measure(s)
- Maximal walking distance to 6 -MWT — at inclusion
Metres walked during 6 minutes - Maximal walking distance to 6 -MWT — at 4 weeks
Metres walked during the test - Maximal walking distance to 6 -MWT — at 8 weeks
Metres walked during the test - Maximal walking distance to 6 -MWT — at 16 weeks
Metres walked during the test
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| CHU de Nice | Nice | France | Recruiting |
More Centre Hospitalier Universitaire de Nice trials in France
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT06443138 on ClinicalTrials.gov ↗ ← All trials in France