Actively Recruiting
Preparation for Medical and Surgical Procedures in Oncogeriatry. Pilote Study PRIMECHO
Led by Centre Hospitalier Universitaire de Nice · Updated on 2026-03-19
20
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Surgical treatment is commonly used for many cancers but can carry a significant risk of complications after surgery, especially in older adults. Maintaining and improving physical abilities before, during, and after treatment is important for elderly cancer patients because better functional capacity is linked to fewer complications. This study focuses on personalizing pre-surgery exercise programs to help patients better adhere and potentially gain more benefits from these programs, aiming to optimize their physical condition before surgery or treatment. Participants will take part in a personalized pre-habilitation program lasting four weeks before their planned surgery. Each day, patients will independently complete a session at home using a special app called Activiti Pro on their tablet or smartphone. This individualized training is designed to manage their exercise load and fatigue to improve adherence and outcomes. During the study, researchers will assess participants' maximum walking distance using the 6-minute walk test at the start and at 4, 8, and 16 weeks. They will also measure quality of life, fatigue levels, and physical activity through questionnaires at these same time points. This monitoring will help understand how the personalized program affects functional abilities and recovery. The total duration of involvement includes the pre-surgery training and follow-up assessments over 16 weeks.
CONDITIONS
Brief Title
Preparation for Medical and Surgical Procedures in Oncogeriatry.
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patient aged 70 or over
- Cancer patient with planned surgery
- Mini Mental State Examination score 24 or higher
- Patient affiliated with or benefiting from social security insurance
- Signed free and informed consent
You will not qualify if you...
- Inability to walk or perform unsupervised exercises
- Vulnerable people
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 4 weeks
Participants follow a personalized pre-habilitation program at home using a dedicated application, completing one session per day for 4 weeks before surgery.
Daily sessions completed independently at home
Trial Site Locations
Total: 1 location
1
CHU de Nice
Nice, France
Actively Recruiting
Research Team
R
Rabia Boulahssass, MD
F
Frédéric Chorin
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
PREVENTION
Number of Arms
1
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