Assessment of the Feasibility and Organisational Impact of a Care Pathway Incorporating the MultiSense® Medical Device for Post-operative Home Monitoring of Elderly Patients.
Recruiting
N/AInterventional Study
Average Length of StaySurgery
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
65 and older
Sex
Any
Study type
Interventional
Purpose
Other
Participants needed
80 (estimated)
Sponsor
Rhythm Diagnostic Systems · Industry
Who this trial is looking for
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Assessing the clinical and organisational impact of a home-based post-operative monitoring strategy incorporating the MultiSense® device involving 80 patients aged 65 years and over who have undergone major surgery.
Trial Locations
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Status
Eligibility Criteria
Inclusion Criteria :
* Patient aged 65 or over
* Patient eligible for remote monitoring using the MultiSense® device
* No psychiatric illness that would prevent them from giving informed consent or receiving optimal treatment and follow-up care
* Subject affiliated with a health insurance scheme
* …
Inclusion Criteria :
* Patient aged 65 or over
* Patient eligible for remote monitoring using the MultiSense® device
* No psychiatric illness that would prevent them from giving informed consent or receiving optimal treatment and follow-up care
* Subject affiliated with a health insurance scheme
* Subject able to read and understand English
* Subject who has signed an informed consent form
* Subjects indicated for scheduled surgery
* Patients indicated for scheduled surgery :
* Transverse colectomy, by laparotomy
* Hepatic laparoscopy
* Laparoscopic or laparoscopic liver surgery (code hlfc or hlfa for procedures)
* Hysterectomy
* Adnexectomy
* Parietal surgery (eventration)
* Rectal resection
* Right and left colectomy
* Stoma closure by direct approach
Exclusion Criteria :
* Patients already participating in an interventional clinical trial.
* Patients subject to legal protection measures, guardianship, curatorship, or deprived of their liberty by judicial or administrative decision.
* Patients hospitalised without consent.
* Patients unable to complete a questionnaire and without a close relative to assist them in using the solution.
* Patients admitted to or residing in a health or social care facility (other than for the surgery itself).
* Persons admitted to or residing in a health or social care institution (other than for the surgery itself);
* Persons unable to give their free and informed consent.
Contacts
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