Preparing elderly cancer patients for surgery
Preparation for Medical and Surgical Procedures in Oncogeriatry. Pilote Study PRIMECHO
This study is testing a personalized training program to help older cancer patients get stronger and recover better before and after surgery.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 20 (estimated) |
| Ages | 70 Years and up |
| Sex | All |
| Sponsor | Centre Hospitalier Universitaire de Nice Academic / other |
| Locations | 1 site (Nice) |
| Trial ID | NCT06443138 on ClinicalTrials.gov |
What this trial studies
This study focuses on optimizing the functional abilities of elderly cancer patients before, during, and after surgical procedures. It aims to implement a personalized pre-habilitation program that addresses individual training loads and fatigue management to enhance patient adherence and outcomes. By tailoring interventions to the specific needs of patients aged 70 and over, the study seeks to reduce postoperative complications associated with surgical management in geriatric oncology. The approach is based on existing literature that highlights the benefits of pre- and post-operative training programs.
Who should consider this trial
Good fit: Ideal candidates for this study are cancer patients aged 70 or older who are scheduled for surgery and have a Mini Mental State Examination score of 24 or higher.
Not a fit: Patients who are unable to walk or perform unsupervised exercises, as well as those considered vulnerable, may not benefit from this study.
Why it matters
Potential benefit: If successful, this program could significantly reduce postoperative complications and improve recovery outcomes for elderly cancer patients.
How similar studies have performed: Previous studies have shown benefits from pre- and post-operative training programs, but this specific individualized approach is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
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
Where this trial is running
Nice
- CHU de Nice — Nice, France (Recruiting)
Study contacts
- Principal investigator: Rabia Boulahssass, MD — Centre Hospitalier Universitaire de Nice
- Study coordinator: Rabia Boulahssass, MD
- Email: boulahssass.r@chu-nice.fr
- Phone: 04 92 03 41 94
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.