Ireland
--:--IST
Recruiting Not applicable

Preparation for Medical and Surgical Procedures in Oncogeriatry.

NCT06443138 · tracked via the Priya Life Science France tracker
Phase
Not applicable
Started
2026-09-11
Last updated
2026-09-14

Condition(s) studied

Geriatric Oncology

Investigational drug(s) / intervention(s)

Personalized pre-habilitation program

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

Sex
ALL
Min age
70 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patient aged 70 or over * Cancer patient with planned surgery, * Mini Mental State Examination score greater than or equal to 24 (performed in advance by the geriatrician), * Patient affiliated to or benefiting from a social security insurance * Signed free and informed consent. Exclusion Criteria: * Inability to walk or perform unsupervised exercises. * Vulnerable people

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)

FacilityCityRegionStatus
CHU de Nice Nice France Recruiting

Other trials for the same condition

Official registry record

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