Actively Recruiting

Phase Not Applicable
Age: 70Years +
All Genders
ID06443138

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

Age: 70Years +
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

You will not qualify if you...

  • Inability to walk or perform unsupervised exercises
  • Vulnerable people

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Personalized Pre-habilitation Program

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

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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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