This is a monocentric, prospective cohort study evaluating the feasibility of a perioperative e-follow-up protocol in patients with ambulatory surgery for breast cancer. This protocol will be based on: * A coordinated ambulatory follow-up performed by a dedicated nurse * An electronic follow-up tool used in pre- and post-surgery Patients will be followed 8 days before the surgery until 30 days after the surgery of breast cancer.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE
Enrollment
40
In pre- and post-surgery: * Completion of questionnaires using an electronic tool, * Telephone follow-up if necessary between the nurse and the patient.
Institut Claudius Regaud IUCT-ONCOPOLE
Toulouse, France
Rate of patients without failure to the e-follow-up. A failure is defined by absence of connection to the electronic tool and the mismatch between the alert level and severity of complications.
Time frame: 1.5 months by patient
Patient satisfaction to the e-follow-up.
Satisfaction will be evaluated by questionnaire.
Time frame: 1.5 months by patient
The rate of patients who discontinue the study 8 days before the surgery.
Time frame: 1.5 months by patient
The number of unplanned visits into the Center after ambulatory surgery in the first 24 hours and during the first 30 days will be assessed for each patient.
Time frame: 1.5 months by patient
Rate of patients with at least one unplanned visit.
Time frame: 1.5 months by patient
The time spent by the dedicated nurse for the follow-up protocol management.
It will be defined as the sum of the time spent at different stages: initial training of patients, tracking of the connections to the tool, tracking of the alerts and telephone contacts.
Time frame: 1.5 months by patient
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